Mapping recombination cold spots in wheat via meiotic recombination in a large biparental population.

Authors: Shaltouki-Rizi M; Department of Agronomy, Purdue University, 915 West State Street, West Lafayette, IN 47907, United States., Dewitt N; School of Plant, Environmental and Soil Sciences, Louisiana State University, 104 Sturgis Hall, Baton Rouge, LA 70803, United States., Mohammadi M; Department of Agronomy, Purdue University, 915 West State Street, West Lafayette, IN 47907, United States.

Source: G3 (Bethesda, Md.) [G3 (Bethesda)] 2026 Jul 06; Vol. 16 (7).

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 101566598 Publication Model: Print Cited Medium: Internet ISSN: 2160-1836 (Electronic) Linking ISSN: 21601836 NLM ISO Abbreviation: G3 (Bethesda) Subsets: MEDLINE

MeSH Terms: Triticum*/genetics , Meiosis*/genetics , Chromosome Mapping* , Recombination, Genetic*, Chromosomes, Plant ; Polymorphism, Single Nucleotide ; Crossing Over, Genetic ; Genome, Plant ; Genetic Linkage ; Quantitative Trait Loci

Recent Advances in Genetic Testing and Clinical Management of Hereditary Breast and Ovarian Cancer (HBOC) in India.

Authors: Sherigar P; Department of Medical Oncology, Manipal Comprehensive Cancer Care Centre, Kasturba Medical College (KMC), Manipal Academy of Higher Education, Manipal, Karnataka, India., Kedlaya Herga S; Department of Public Health Genomics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India., Pai A; Department of Medical Oncology, Manipal Comprehensive Cancer Care Centre, Kasturba Medical College (KMC), Manipal Academy of Higher Education, Manipal, Karnataka, India., Mailankody S; Department of Medical Oncology, Manipal Comprehensive Cancer Care Centre, Kasturba Medical College (KMC), Manipal Academy of Higher Education, Manipal, Karnataka, India., Udupa KS; Department of Medical Oncology, Manipal Comprehensive Cancer Care Centre, Kasturba Medical College (KMC), Manipal Academy of Higher Education, Manipal, Karnataka, India.

Source: Cancer medicine [Cancer Med] 2026 Jul; Vol. 15 (7), pp. e71497.

Publication Type: Journal Article; Review

Journal Info: Publisher: John Wiley & Sons Ltd Country of Publication: United States NLM ID: 101595310 Publication Model: Print Cited Medium: Internet ISSN: 2045-7634 (Electronic) Linking ISSN: 20457634 NLM ISO Abbreviation: Cancer Med Subsets: MEDLINE

MeSH Terms: Genetic Testing*/methods , Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis , Hereditary Breast and Ovarian Cancer Syndrome*/therapy , Hereditary Breast and Ovarian Cancer Syndrome*/epidemiology, India/epidemiology ; Ovarian Neoplasms/genetics ; BRCA2 Protein/genetics ; BRCA1 Protein/genetics ; Humans ; Female ; Genetic Predisposition to Disease ; Genetic Counseling ; Mutation ; Disease Management

Prenatal Diagnosis and Novel Therapeutics in Treatment of Genetic Conditions: Challenges and Opportunities.

Authors: Talati AN; Maternal Fetal Medicine & Reproductive Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina. Electronic address: asha_talati@med.unc.edu., Jones M; Maternal Fetal Medicine & Reproductive Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina., Hardisty EE; Maternal Fetal Medicine & Reproductive Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina., Michie M; Department of Bioethics, Case Western Reserve University School Of Medicine, Cleveland, Ohio., Allyse MA; Department of Bioethics, Case Western Reserve University School Of Medicine, Cleveland, Ohio., Vora NL; Maternal Fetal Medicine & Reproductive Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Source: Clinical therapeutics [Clin Ther] 2026 Jul; Vol. 48 (7), pp. 583-587. Date of Electronic Publication: 2026 Jun 06.

Publication Type: Journal Article; Review

Journal Info: Publisher: Excerpta Medica Country of Publication: United States NLM ID: 7706726 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-114X (Electronic) Linking ISSN: 01492918 NLM ISO Abbreviation: Clin Ther Subsets: MEDLINE

MeSH Terms: Prenatal Diagnosis*/ethics , Prenatal Diagnosis*/methods , Genetic Therapy*/methods , Genetic Therapy*/ethics , Genetic Diseases, Inborn*/diagnosis , Genetic Diseases, Inborn*/therapy , Genetic Diseases, Inborn*/genetics, Humans ; Pregnancy ; Female ; United States ; Genetic Counseling ; Genetic Testing

An interactive human PROS1 variants database provides novel insights into the genetics and phenotypes of inherited protein S deficiency.

Authors: Hou Z; Department of hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China; Department of Pathology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China; International Center for Aging and Cancer, Hainan Academy of Medical Sciences, Hainan Medical University, Haikou, Hainan, People's Republic of China., Liu F; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Dong S; Department of hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Guo Y; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Yu X; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Ai LJ; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Zhang M; Department of Pathology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Kang J; Department of Pathology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Jiang B; Department of Pathology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Dong Y; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Zhao M; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China; Department of Neurology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Pan J; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Zhang S; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China., Zhao W; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China. Electronic address: zhaowr@hrbmu.edu.cn., Wang W; Department of hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China. Electronic address: ww0543@163.com., Hao D; Department of Pathology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China. Electronic address: dapenghao@hrbmu.edu.cn., Shen G; Department of hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China; Department of Cell Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin, Heilongjiang, People's Republic of China. Electronic address: shenba433@163.com.

Source: Journal of thrombosis and haemostasis : JTH [J Thromb Haemost] 2026 Jul; Vol. 24 (7), pp. 2579-2592. Date of Electronic Publication: 2026 Apr 10.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 101170508 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1538-7836 (Electronic) Linking ISSN: 15387836 NLM ISO Abbreviation: J Thromb Haemost Subsets: MEDLINE

MeSH Terms: Protein S Deficiency*/genetics , Protein S Deficiency*/blood , Protein S Deficiency*/diagnosis , Protein S Deficiency*/epidemiology , Blood Proteins*/genetics , Databases, Genetic* , Genetic Variation*, Thrombosis/genetics ; Thrombosis/blood ; Thrombosis/epidemiology ; Protein S/metabolism ; Humans ; Phenotype ; Genetic Predisposition to Disease ; Genetic Association Studies ; Risk Factors ; Female ; Age of Onset ; Risk Assessment ; Male ; Mutation ; Adult

Knowledge of cancer genetics and attitudes about genetic counseling and testing: a randomized trial of the Know Your Risk intervention compared to conventional genetic counseling.

Authors: Katz ML; Division of Health Behavior and Health Promotion, College of Public Health, The Ohio State University, Columbus, OH, USA. mira.katz@osumc.edu.; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA. mira.katz@osumc.edu.; The Ohio State University, Room 212, 3650 Olentangy River Road, Columbus, OH, 43214, USA. mira.katz@osumc.edu., Schnell PM; Division of Biostatistics, College of Public Health, The Ohio State University, Columbus, OH, USA., Reiter PL; Division of Health Behavior and Health Promotion, College of Public Health, The Ohio State University, Columbus, OH, USA.; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA., Senter L; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Aeilts A; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Spears C; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Cooper J; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Brown J; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Shane-Carson KP; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Agnese DM; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.; Department of Surgery, College of Medicine, The Ohio State University, Columbus, OH, USA., Toland AE; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.; Department of Cancer Biology and Genetics, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Sweet K; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.

Source: Cancer causes & control : CCC [Cancer Causes Control] 2026 Jun 30; Vol. 37 (7). Date of Electronic Publication: 2026 Jun 30.

Publication Type: Journal Article; Randomized Controlled Trial

Journal Info: Publisher: Kluwer Academic Publishers Country of Publication: Netherlands NLM ID: 9100846 Publication Model: Electronic Cited Medium: Internet ISSN: 1573-7225 (Electronic) Linking ISSN: 09575243 NLM ISO Abbreviation: Cancer Causes Control Subsets: MEDLINE

MeSH Terms: Genetic Counseling*/methods , Genetic Counseling*/psychology , Genetic Testing*/methods , Breast Neoplasms*/genetics , Breast Neoplasms*/psychology , Breast Neoplasms*/diagnosis , Health Knowledge, Attitudes, Practice*, Humans ; Female ; Middle Aged ; Adult ; Genetic Predisposition to Disease ; Surveys and Questionnaires

Expanded carrier screening in a Southwestern Chinese population indicates East Asian specific low-frequency pathogenic variants account for nearly half of the at-risk couple rate.

Authors: Liu S; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Cao L; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Zhang VW; AmCare Genomics Lab, Guangzhou, Guangdong, China., Huang S; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Liu H; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Wei X; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Luo Y; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Li Y; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Zhou L; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Jiang L; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Zhu Q; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China hongqian.liu@163.com zhuqian_2009@163.com.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China., Liu H; Department of Medical Genetics, Sichuan University West China Second University Hospital Department of Medical Genetics, Chengdu, Sichuan, China hongqian.liu@163.com zhuqian_2009@163.com.; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China.

Source: Journal of medical genetics [J Med Genet] 2026 Jun 25; Vol. 63 (7), pp. 447-455. Date of Electronic Publication: 2026 Jun 25.

Publication Type: Journal Article

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

MeSH Terms: Genetic Carrier Screening*/methods , Asian People*/genetics, Gene Frequency/genetics ; China/epidemiology ; Connexin 26/genetics ; Humans ; Male ; Female ; Heterozygote ; East Asian People ; Genetic Testing ; Alleles ; Genetic Predisposition to Disease ; Mutation

Reverse haplotyping: taking full advantage of 25% risk testing for the 50% at-risk parent in Huntington's disease.

Authors: Bijlsma EK; Clinical Genetics, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands e.k.bijlsma@lumc.nl., Koopmann TT; Clinical Genetics, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands., de Bot ST; Neurology, Leiden University Medical Center, Leiden, The Netherlands., Losekoot M; Clinical Genetics, Leiden University Medical Center, Leiden, Zuid-Holland, The Netherlands.

Source: Journal of medical genetics [J Med Genet] 2026 Jun 25; Vol. 63 (7), pp. 463-465. Date of Electronic Publication: 2026 Jun 25.

Publication Type: Journal Article

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

MeSH Terms: Huntington Disease*/genetics , Huntington Disease*/diagnosis , Genetic Testing*/methods , Haplotypes*/genetics , Genetic Predisposition to Disease*, Humans ; Female ; Pregnancy ; Genetic Counseling ; Prenatal Diagnosis ; Parents

Introgression and Divergence in a Young Species Group.

Authors: Satokangas I; Organismal & Evolutionary Biology Research Programme, University of Helsinki, Helsinki, Finland.; Institute of Ecology and Evolution, Ashworth Laboratories, University of Edinburgh, Edinburgh, UK., Martin SH; Institute of Ecology and Evolution, Ashworth Laboratories, University of Edinburgh, Edinburgh, UK., Seifert B; Department of Entomology, Senckenberg Museum für Naturkunde, Görlitz, Germany., Puukko T; Organismal & Evolutionary Biology Research Programme, University of Helsinki, Helsinki, Finland., Schultz R; Department of Entomology, Senckenberg Museum für Naturkunde, Görlitz, Germany., Helanterä H; Ecology and Genetics Research Unit, University of Oulu, Oulu, Finland., Kulmuni J; Organismal & Evolutionary Biology Research Programme, University of Helsinki, Helsinki, Finland.; Tvärminne Zoological Station, University of Helsinki, Hanko, Finland.; Institute for Biodiversity and Ecosystem Dynamics, Department of Evolutionary and Population Biology, University of Amsterdam, Amsterdam, the Netherlands.

Source: Molecular ecology [Mol Ecol] 2026 Jun; Vol. 35 (12), pp. e70448.

Publication Type: Journal Article

Journal Info: Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 9214478 Publication Model: Print Cited Medium: Internet ISSN: 1365-294X (Electronic) Linking ISSN: 09621083 NLM ISO Abbreviation: Mol Ecol Subsets: MEDLINE

MeSH Terms: Ants*/genetics , Ants*/classification , Genetic Speciation* , Genetic Introgression*, DNA, Mitochondrial/genetics ; Animals ; Gene Flow ; Phylogeny ; Models, Genetic ; Sequence Analysis, DNA ; Hybridization, Genetic ; Genetic Variation ; Reproductive Isolation ; Genetics, Population

Genetic diversity and population structure of Passiflora spp. using inter-primer binding site (iPBS) - retrotransposon markers.

Authors: de Jesus ON; Embrapa Mandioca e Fruticultura, Rua Embrapa, s/n, Cruz das Almas, P.O. Box 007, Chapadinha, Bahia, 44380-000, Brazil. onildo.nunes@embrapa.br., Costa EMR; Embrapa Mandioca e Fruticultura, Rua Embrapa, s/n, Cruz das Almas, P.O. Box 007, Chapadinha, Bahia, 44380-000, Brazil., Azevedo FQ; Embrapa Clima Temperado, BR 392, km 78 - 9º Distrito, Monte Bonito, P.O. Box 403, Pelotas, 96010-971, Rio Grande do Sul, Brazil., de Sousa VR; Embrapa Mandioca e Fruticultura, Rua Embrapa, s/n, Cruz das Almas, P.O. Box 007, Chapadinha, Bahia, 44380-000, Brazil., Gonçalves ZS; Embrapa Mandioca e Fruticultura, Rua Embrapa, s/n, Cruz das Almas, P.O. Box 007, Chapadinha, Bahia, 44380-000, Brazil., Lima LKS; Universidade Estadual de Feira de Santana, Av. Transnordestina, s/n, Novo Horizonte, Feira de Santana, Bahia, 44036-900, Brazil., Soares TL; Embrapa Mandioca e Fruticultura, Rua Embrapa, s/n, Cruz das Almas, P.O. Box 007, Chapadinha, Bahia, 44380-000, Brazil.

Source: Molecular biology reports [Mol Biol Rep] 2026 Jun 01; Vol. 53 (1). Date of Electronic Publication: 2026 Jun 01.

Publication Type: Journal Article

Journal Info: Publisher: Reidel Country of Publication: Netherlands NLM ID: 0403234 Publication Model: Electronic Cited Medium: Internet ISSN: 1573-4978 (Electronic) Linking ISSN: 03014851 NLM ISO Abbreviation: Mol Biol Rep Subsets: MEDLINE

MeSH Terms: Passiflora*/genetics , Genetic Variation*/genetics , Retroelements*/genetics, Genetics, Population/methods ; Binding Sites/genetics ; Genetic Markers/genetics ; DNA Primers/genetics ; Genotype ; Phylogeny ; Polymorphism, Genetic ; Alleles ; Principal Component Analysis ; Cluster Analysis

Optimising POU3F4 variant interpretation through gene-specific evidence in X-linked hearing loss.

Authors: Geng J; Department of Otolaryngology-Head and Neck Surgery, West China Hospital, Sichuan University, Chengdu, China; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Zhao Y; Department of Otolaryngology, Head and Neck Surgery, People's Hospital, Peking University, Beijing, China., Huang Y; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Xiong W; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Zhong M; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Wang C; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Wang X; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Zhang Q; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Tang T; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Chen M; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China; Brain Hospital of Hunan Province (The Second People's Hospital of Hunan Province), Hunan, China., Fang L; Genomics Center, Core Facility of West China Hospital, Sichuan University, Chengdu, China., Yang Y; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China., Bu F; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China. Electronic address: bufengxiao@wchscu.cn., Cheng J; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China. Electronic address: chengjing@wchscu.cn., Lu Y; Department of Otolaryngology-Head and Neck Surgery, West China Hospital, Sichuan University, Chengdu, China; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China. Electronic address: luyu@wchscu.cn., Yuan H; Department of Otolaryngology-Head and Neck Surgery, West China Hospital, Sichuan University, Chengdu, China; Institute of Rare Diseases, West China Hospital, Sichuan University, Chengdu, China. Electronic address: yuanhj301@wchscu.cn.

Source: EBioMedicine [EBioMedicine] 2026 Jun; Vol. 128, pp. 106318. Date of Electronic Publication: 2026 May 29.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier B.V Country of Publication: Netherlands NLM ID: 101647039 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2352-3964 (Electronic) Linking ISSN: 23523964 NLM ISO Abbreviation: EBioMedicine Subsets: MEDLINE

MeSH Terms: POU Domain Factors*/genetics , POU Domain Factors*/chemistry , Hearing Loss*/genetics , Hearing Loss*/diagnosis , Genetic Diseases, X-Linked*/genetics , Genetic Diseases, X-Linked*/diagnosis , Genetic Variation*, Humans ; Genetic Association Studies ; Bayes Theorem ; Mutation ; Polymorphism, Single Nucleotide ; Female ; Male ; Phenotype ; Genetic Predisposition to Disease ; Alleles

Breast cancer patients' experiences and outcomes of mainstream genetic testing with and without genetic counseling.

Authors: Beard C; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australia.; Department of Medicine, The University of Melbourne, Melbourne, VIC, Australia., Monohan K; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australia., Lang N; Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia., Cicciarelli L; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australia., James PA; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australia.; Department of Medicine, The University of Melbourne, Melbourne, VIC, Australia.; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia., Forrest LE; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australia.; Department of Medicine, The University of Melbourne, Melbourne, VIC, Australia.; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia.

Source: Future oncology (London, England) [Future Oncol] 2026 Jun; Vol. 22 (14), pp. 1703-1710. Date of Electronic Publication: 2026 May 27.

Publication Type: Journal Article

Journal Info: Publisher: Taylor & Francis Country of Publication: England NLM ID: 101256629 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-8301 (Electronic) Linking ISSN: 14796694 NLM ISO Abbreviation: Future Oncol Subsets: MEDLINE

MeSH Terms: Genetic Counseling*/psychology , Breast Neoplasms*/genetics , Breast Neoplasms*/psychology , Breast Neoplasms*/diagnosis , Genetic Testing*/methods , Genetic Testing*/statistics & numerical data, Humans ; Female ; Middle Aged ; Adult ; Decision Making ; Aged ; Genetic Predisposition to Disease ; Surveys and Questionnaires

The Time Invariance and Nondecreasing Expectation of an Evolutionary Path Characteristic under Weak Selection.

Authors: Yu YY; School of Mathematics and Statistics, Northwestern Polytechnical University, Xi'an 710072, China., Hui C; Department of Mathematical Sciences, Stellenbosch University, Stellenbosch 7602, South Africa; National Institute for Theoretical and Computational Sciences, African Institute for Mathematical Sciences, Stellenbosch 7602, South Africa; and International Initiative for Theoretical Ecology, London N1 2EE, United Kingdom., Feng TJ; Key Laboratory of Animal Ecology and Conservation Biology, Center for Computational and Evolutionary Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China., Li C; School of Ecology and Environment, Northwestern Polytechnical University, Xi'an 710072, China., Wang C; School of Ecology and Environment, Northwestern Polytechnical University, Xi'an 710072, China., Tao Y; Key Laboratory of Animal Ecology and Conservation Biology, Center for Computational and Evolutionary Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; School of Ecology and Environment, Northwestern Polytechnical University, Xi'an 710072, China., Wang RW; College of Life Sciences, Zhejiang University, Hangzhou 310058, China.

Source: The American naturalist [Am Nat] 2026 Jun; Vol. 207 (6), pp. 860-869. Date of Electronic Publication: 2026 Mar 31.

Publication Type: Journal Article

Journal Info: Publisher: University of Chicago Press Country of Publication: United States NLM ID: 2984688R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-5323 (Electronic) Linking ISSN: 00030147 NLM ISO Abbreviation: Am Nat Subsets: MEDLINE

MeSH Terms: Selection, Genetic* , Biological Evolution* , Genetic Fitness*, Genetic Drift ; Phenotype ; Stochastic Processes ; Models, Genetic

An interdisciplinary Inherited Retinal Disease clinic improves time to genetic diagnosis and access to genetics services.

Authors: Goldin MR; Department of Ophthalmology and Visual Sciences, Vanderbilt University School of Medicine, Nashville, Tennessee, USA., Suh H; Department of Ophthalmology and Visual Sciences, Vanderbilt University School of Medicine, Nashville, Tennessee, USA., Kessler C; Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute, Nashville, Tennessee, USA., Dones A; Department of Ophthalmology and Visual Sciences, Vanderbilt University School of Medicine, Nashville, Tennessee, USA., Zubieta D; Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute, Nashville, Tennessee, USA., Decker J; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA., Brantley MA Jr; Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute, Nashville, Tennessee, USA.

Source: Ophthalmic genetics [Ophthalmic Genet] 2026 Jun; Vol. 47 (3), pp. 268-274. Date of Electronic Publication: 2026 Feb 23.

Publication Type: Journal Article

Journal Info: Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE

MeSH Terms: Genetic Testing*/statistics & numerical data , Retinal Diseases*/diagnosis , Retinal Diseases*/genetics , Health Services Accessibility*/statistics & numerical data , Genetic Services*/statistics & numerical data , Genetic Services*/organization & administration, Genetic Counseling/statistics & numerical data ; Humans ; Female ; Retrospective Studies ; Male ; Adult ; Middle Aged ; Referral and Consultation ; Adolescent ; Young Adult ; Aged

Optimum recombination rates for genetic gains in simulated recurrent selection in empirical maize populations.

Authors: Anilkumar C; Department of Agronomy and Plant Genetics, University of Minnesota, Saint Paul, Minnesota, USA.; Indian Council of Agricultural Research-Central Rice Research Institute, Cuttack, India., Bernardo R; Department of Agronomy and Plant Genetics, University of Minnesota, Saint Paul, Minnesota, USA.

Source: The plant genome [Plant Genome] 2026 Jun; Vol. 19 (2), pp. e70229.

Publication Type: Journal Article

Journal Info: Publisher: Crop Science Society of America Country of Publication: United States NLM ID: 101273919 Publication Model: Print Cited Medium: Internet ISSN: 1940-3372 (Electronic) Linking ISSN: 19403372 NLM ISO Abbreviation: Plant Genome Subsets: MEDLINE

MeSH Terms: Zea mays*/genetics , Recombination, Genetic* , Selection, Genetic*, Haplotypes ; Polymorphism, Single Nucleotide ; Crossing Over, Genetic ; Phenotype ; Genetic Linkage

Genetic Susceptibility to Neurodevelopmental Conditions Is Associated With Neonatal DNA Methylation Patterns in the General Population: An Individual Participant Data Meta-Analysis.

Authors: Schuurmans IK; Department of Epidemiology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Generation R Study Group, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands., Smajlagic D; PROMENTA Research Centre, Department of Psychology, University of Oslo, Oslo, Norway., Baltramonaityte V; Department of Psychology, University of Bath, Bath, United Kingdom., Malmberg ALK; Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland., Neumann A; Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands., Creasey N; Generation R Study Group, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Division of Psychology & Language Sciences, Department of Clinical, Educational, and Health Psychology, University College London, London, United Kingdom., Felix JF; Generation R Study Group, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Department of Pediatrics, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands., Tiemeier H; Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Department of Social and Behavioral Sciences, Harvard TH Chan School of Public Health, Boston, Massachusetts., Pingault JB; Division of Psychology & Language Sciences, Department of Clinical, Educational, and Health Psychology, University College London, London, United Kingdom; Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom., Czamara D; Department Genes and Environment, Max-Planck-Institute of Psychiatry, Munich, Germany., Raïkkönen K; Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Department of Obstetrics and Gynecology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland., Page CM; Centre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway., Lyle R; Centre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway., Havdahl A; PsychGen Centre for Genetic Epidemiology and Mental Health, Norwegian Institute of Public Health, Oslo, Norway; Nic Waals Institute, Lovisenberg Diaconal Hospital, Oslo, Norway., Lahti J; Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland., Walton E; Department of Psychology, University of Bath, Bath, United Kingdom., Bekkhus M; PROMENTA Research Centre, Department of Psychology, University of Oslo, Oslo, Norway., Cecil CAM; Department of Epidemiology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands; Molecular Epidemiology, Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: c.cecil@erasmusmc.nl.

Source: Biological psychiatry [Biol Psychiatry] 2026 Aug 15; Vol. 100 (4), pp. 414-425. Date of Electronic Publication: 2025 Sep 22.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 0213264 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2402 (Electronic) Linking ISSN: 00063223 NLM ISO Abbreviation: Biol Psychiatry Subsets: MEDLINE

MeSH Terms: DNA Methylation*/genetics , Schizophrenia*/genetics , Autism Spectrum Disorder*/genetics , Attention Deficit Disorder with Hyperactivity*/genetics , Neurodevelopmental Disorders*/genetics , Genetic Predisposition to Disease*, Humans ; Female ; Genetic Risk Score ; Infant, Newborn ; Male ; Child ; Adolescent ; Child, Preschool ; Epigenesis, Genetic ; Fetal Blood ; Infant

Genetics and Screening in Prostate Cancer.

Authors: Partuzo JGR; Department of Urology, Georgetown University School of Medicine, Washington, DC, USA., Mora-Garijo B; Department of Urology, Medstar Georgetown University Hospital, Washington Hospital Center, Washington, DC, USA., Hwang J; Department of Urology, Georgetown University School of Medicine, Washington, DC, USA. Electronic address: Jonathan.J.Hwang@medstar.net.

Source: The Surgical clinics of North America [Surg Clin North Am] 2026 Aug; Vol. 106 (4), pp. 603-617. Date of Electronic Publication: 2026 May 27.

Publication Type: Journal Article; Review

Journal Info: Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0074243 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-3171 (Electronic) Linking ISSN: 00396109 NLM ISO Abbreviation: Surg Clin North Am Subsets: MEDLINE

MeSH Terms: Prostatic Neoplasms*/genetics , Prostatic Neoplasms*/diagnosis , Genetic Testing*/methods , Early Detection of Cancer*/methods, Humans ; Male ; Genetic Predisposition to Disease ; Genetic Risk Score ; Prognosis

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations.

Authors: Diogo-Cavassana S; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Alencar-Coutinho D; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Abreu-Oberhuber R; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Paramo-Neto ME; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Oiticica J; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Bento RF; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Batissoco AC; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Lezirovitz K; Laboratório de Otorrinolaringologia Genética Molecular, Celular e Translacional/LIM32, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.; Otorhinolaryngology Department, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Source: Clinical genetics [Clin Genet] 2026 Aug; Vol. 110 (2), pp. 210-226. Date of Electronic Publication: 2026 Jun 03.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

MeSH Terms: Hearing Loss*/genetics , Hearing Loss*/epidemiology , Hearing Loss*/diagnosis , Genetic Predisposition to Disease*, Brazil/epidemiology ; Myosins/genetics ; Connexins/genetics ; Humans ; Female ; Myosin VIIa ; Male ; Mutation ; Connexin 26 ; Phenotype ; High-Throughput Nucleotide Sequencing ; Gene Frequency ; Genetic Association Studies ; Child ; Genetic Testing ; Child, Preschool ; Adolescent

Genetic Diversity and Population Structure of Tunisian Festuca Arundinacea Schreb. Revealed by Functional Gene-Based Markers.

Authors: Chadded H; Faculté des Sciences de Tunis, Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie (LR99ES12), Université de Tunis El Manar, Campus Universitaire Farhat Hached, 2092, El Manar, Tunis, Tunisia., Guenni K; Faculté des Sciences de Tunis, Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie (LR99ES12), Université de Tunis El Manar, Campus Universitaire Farhat Hached, 2092, El Manar, Tunis, Tunisia., Crespan M; CREA Research Centre for Viticulture and Enology, Viale XXVIII Aprile, 26, 31015, Conegliano, Italy., Sai-Kachout S; Laboratoire des Productions Animales et Fourragères, Institut National de la Recherche Agronomique de Tunisie, Université de Carthage, Rue Hédi Karray El Menzah, 1004, Tunis, Tunisia., Chtourou-Ghorbel N; Faculté des Sciences de Tunis, Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie (LR99ES12), Université de Tunis El Manar, Campus Universitaire Farhat Hached, 2092, El Manar, Tunis, Tunisia. nidhal.ghorbel@issbat.utm.tn.

Source: Biochemical genetics [Biochem Genet] 2026 Aug; Vol. 64 (4), pp. 5843-5867. Date of Electronic Publication: 2026 Jan 20.

Publication Type: Journal Article

Journal Info: Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 0126611 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-4927 (Electronic) Linking ISSN: 00062928 NLM ISO Abbreviation: Biochem Genet Subsets: MEDLINE

MeSH Terms: Festuca*/genetics , Genetic Variation* , Polymorphism, Genetic*, Tunisia ; Genetic Markers ; Genetics, Population ; Phylogeny

A multidisciplinary model for implementation of nephrogenetics in CKD outpatients: a clinical and data-driven perspective.

Authors: Mazzierli T; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy., Tsalouchos A; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy., Gallo P; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy., Somma C; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy., Mehmetaj A; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy., Pizzarelli F; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy., Pelo E; Diagnostic Genetic Unit, Careggi University Hospital, Florence 50134, Italy., Giuliani C; Diagnostic Genetic Unit, Careggi University Hospital, Florence 50134, Italy., Dattolo P; Nephrology and Dialysis Unit Firenze 2, Department of Medical Specialties, Azienda Usl Toscana Centro, Firenze 50100, Italy.

Source: Journal of nephrology [J Nephrol] 2026 Jul 31; Vol. 39 (3), pp. 512-518.

Publication Type: Journal Article

Journal Info: Publisher: Springer Country of Publication: England NLM ID: 9012268 Publication Model: Print Cited Medium: Internet ISSN: 1724-6059 (Electronic) Linking ISSN: 11218428 NLM ISO Abbreviation: J Nephrol Subsets: MEDLINE

MeSH Terms: Patient Care Team*/organization & administration , Renal Insufficiency, Chronic*/therapy , Renal Insufficiency, Chronic*/genetics , Renal Insufficiency, Chronic*/diagnosis , Ambulatory Care*/organization & administration , Nephrology*/organization & administration , Genetic Testing*, Humans ; Female ; Middle Aged ; Male ; Adult ; Aged ; Italy ; Genetic Predisposition to Disease ; Interdisciplinary Communication ; Genetic Counseling ; Phenotype

[Survey on the involvement of Japanese neurologists in genetic medicine].

Authors: Shibata Y; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University., Chang H; Department of Genomic Medicine, The University of Tokyo Hospital., Yamada S; Department of Neurology, Nagoya University Graduate School of Medicine., Matsushima M; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.; Health Care Center, Hokkaido University., Saigoh K; Department of Clinical genetics, Kindai University Hospital., Ishiura H; Department of Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences., Sekijima Y; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine., Maruyama H; Department of Clinical Neuroscience and Therapeutics, Hiroshima University Graduate School of Biomedical and Health Sciences., Ikeuchi T; Department of Molecular Genetics, Brain Research Institute, Niigata University., Hasegawa K; Department of Neurology, National Hospital Organization, Sagamihara National Hospital., Aoki M; Department of Neurology, Tohoku University Graduate School of Medicine., Katsuno M; Department of Neurology, Nagoya University Graduate School of Medicine., Toda T; National Center Hospital, National Center of Neurology and Psychiatry., Yabe I; Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.

Corporate Authors: Committee on Medical Genetics, Japanese Society of Neurology

Source: Rinsho shinkeigaku = Clinical neurology [Rinsho Shinkeigaku] 2026 Jul 28; Vol. 66 (7), pp. 450-456. Date of Electronic Publication: 2026 Jun 18.

Publication Type: English Abstract; Journal Article

Journal Info: Publisher: Nihon Shinkei Gakkai Country of Publication: Japan NLM ID: 0417466 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1882-0654 (Electronic) Linking ISSN: 0009918X NLM ISO Abbreviation: Rinsho Shinkeigaku Subsets: MEDLINE

MeSH Terms: Genetic Testing*/statistics & numerical data , Genetic Testing*/trends , Neurologists*/statistics & numerical data , Genomic Medicine*/trends , Neurology*, Humans ; Japan ; Surveys and Questionnaires ; Genetic Counseling ; Early Diagnosis ; Prenatal Diagnosis ; Preimplantation Diagnosis ; East Asian People