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Commentary: Using human genetics to guide the repurposing of medicines.

• Authors : Bovijn J; Big Data Institute at the Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK.; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.

Subjects: Alzheimer Disease* ; Antihypertensive Agents*; Drug Repositioning

• Source: International journal of epidemiology [Int J Epidemiol] 2020 Aug 01; Vol. 49 (4), pp. 1140-1146.Publisher: Oxford University Press Country of Publication: England NLM ID: 7802871 Publication Model: Print Cited Medium:

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Commentary: The central questions of human genetics: Richard Lewontin's 1968 senior lecture in Victor McKusick's Bar Harbor short course.

• Authors : Chakravarti A; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Broadway Research Building, Suite 579, 733 N. Broadway, Baltimore, MD 21205, USA. E-mail: .

Subjects: Human Genetics*; Humans

• Source: International journal of epidemiology [Int J Epidemiol] 2016 Jun; Vol. 45 (3), pp. 668-72. Date of Electronic Publication: 2016 Aug 31.Publisher: Oxford University Press Country of Publication: England NLM ID: 7802871 Publication Model: Print-Electronic Cited

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Commentary: Through a glass, darkly-Dick Lewontin's 1968 lecture on human genetics.

• Authors : Cobb M; Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK. .

Subjects: Genetics, Population* ; Human Genetics*; Humans

• Source: International journal of epidemiology [Int J Epidemiol] 2016 Jun; Vol. 45 (3), pp. 664-6.Publisher: Oxford University Press Country of Publication: England NLM ID: 7802871 Publication Model: Print Cited Medium:

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Polympact: exploring functional relations among common human genetic variants.

• Authors : Valentini S; Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.; Gandolfi F

Subjects: Genome-Wide Association Study* ; Human Genetics*; Cluster Analysis

• Source: Nucleic acids research [Nucleic Acids Res] 2022 Feb 22; Vol. 50 (3), pp. 1335-1350.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium:

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When a gene makes you smell like a fish-- and other tales about the genes in your body. [electronic resource]

• Authors : Chiu, Lisa Seachrist; Seachrist, Judith A.; ...

Subjects: Human genetics -- Popular works; Human genetics -- Anecdotes; Electronic books

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The need for interaction between assisted reproduction technology and genetics: recommendations of the European Societies of Human Genetics and Human Reproduction and Embryology

• Authors : European Society of Human Genetics and European Society of Human Reproduction and Embryology

Subjects: ESHRE PAGES

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The Sonoda–Tajima Cell Collection: A Human Genetics Research Resource with Emphasis on South American Indigenous Populations

• Authors : Yukio Nakamura; Inaho Danjoh; Takashi Hiroyama

Subjects: Epstein-Barr Virus Infections; Herpesvirus 4, Human; Resource (biology)

• Source: Genome Biology and Evolution

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DAXX promotes centromeric stability independently of ATRX by preventing the accumulation of R-loop-induced DNA double-stranded breaks

• Authors : Pinto, Lia, M; Pailas, Alexandros; Bondarchenko, Max ...

Subjects: MESH: Adaptor Proteins; Signal Transducing / genetics; Signal Transducing / metabolism

• Source: ISSN: 0305-1048.

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Reconstructing DNA methylation maps of ancient populations.

• Authors : Barouch A; Department of Genetics, The Alexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.; School of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.

Subjects: DNA Methylation*/DNA Methylation*/DNA Methylation*/genetics ; DNA, Ancient*; Humans

• Source: Nucleic acids research [Nucleic Acids Res] 2024 Feb 28; Vol. 52 (4), pp. 1602-1612.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium:

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Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects

• Authors : Werren, Elizabeth; Rodriguez Bey, Guillermo; Majethia, Purvi ...

Subjects: 4.1B; delayed myelination; loss-of-function

• Source: ISSN: 0006-8950.

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