المؤلفون: Werren, Elizabeth, Laforce, Geneva, Srivastava, Anshika, Perillo, Delia, Li, Shaokun, Johnson, Katherine, Baris, Safa, Berger, Brandon, Regan, Samantha, Pfennig, Christian, de Munnik, Sonja, Pfundt, Rolph, Hebbar, Malavika, Jimenez-Heredia, Raúl, Karakoc-Aydiner, Elif, Ozen, Ahmet, Dmytrus, Jasmin, Krolo, Ana, Corning, Ken, Prijoles, E., Louie, Raymond, Lebel, Robert Roger, Le, Thuy-Linh, Amiel, Jeanne, Gordon, Christopher, Boztug, Kaan, Girisha, Katta, Shukla, Anju, Bielas, Stephanie, Schaffer, Ashleigh

المساهمون: University of Michigan Medical School Ann Arbor, University of Michigan Ann Arbor, University of Michigan System-University of Michigan System, The Jackson Laboratory Bar Harbor (JAX), Case Western Reserve University Cleveland, Sanjay Gandhi Postgraduate Institute of Medical Sciences Lucknow, India, Marmara University Kadıköy - İstanbul, Radboud University Medical Center Nijmegen, University of Washington Seattle, Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases (LBI-RUD), Austrian Academy of Sciences (OeAW), The Greenwood Genetic Center, SUNY Upstate Medical University, State University of New York (SUNY), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Hôpital Necker - Enfants Malades AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Medizinische Universität Wien = Medical University of Vienna, Saint Anna Children's Hospital Vienne = St Anna Kinderspital (St. Anna Children's Hospital), Kasturba Medical College, Manipal

المصدر: ISSN: 2041-1723.

مصطلحات موضوعية: [SDV]Life Sciences [q-bio]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38388531; hal-04586623; https://u-paris.hal.science/hal-04586623Test; https://u-paris.hal.science/hal-04586623/documentTest; https://u-paris.hal.science/hal-04586623/file/s41467-024-45948-y.pdfTest; PUBMED: 38388531; PUBMEDCENTRAL: PMC10884030

الإتاحة: https://doi.org/10.1038/s41467-024-45948-yTest
https://u-paris.hal.science/hal-04586623Test
https://u-paris.hal.science/hal-04586623/documentTest
https://u-paris.hal.science/hal-04586623/file/s41467-024-45948-y.pdfTest

المؤلفون: Werren, Elizabeth A., Guxholli, Alba, Jones, Natasha, Wagner, Matias, Hannibal, Iris, Granadillo, Jorge L., Tyndall, Amanda V., Moccia, Amanda, Kuehl, Ryan, Levandoski, Kristin M., Day-Salvatore, Debra L., Wheeler, Marsha, Chong, Jessica X., Bamshad, Michael J., Innes, A. Micheil, Pierson, Tyler Mark, Mackay, Joel P., Bielas, Stephanie L., Martin, Donna M.

المصدر: Human Genetics and Genomics Advances ; volume 4, issue 3, page 100198 ; ISSN 2666-2477

مصطلحات موضوعية: Genetics (clinical), Molecular Medicine

الإتاحة: https://doi.org/10.1016/j.xhgg.2023.100198Test
https://api.elsevier.com/content/article/PII:S2666247723000301?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2666247723000301?httpAccept=text/plainTest

المؤلفون: Werren, Elizabeth A., Peirent, Emily R., Jantti, Henna, Guxholli, Alba, Srivastava, Kinshuk Raj, Orenstein, Naama, Narayanan, Vinodh, Wiszniewski, Wojciech, Dawidziuk, Mateusz, Gawlinski, Pawel, Umair, Muhammad, Khan, Amjad, Khan, Shahid Niaz, Geneviève, David, Lehalle, Daphné, van Gassen, K. L. I., Giltay, Jacques C., Oegema, Renske, van Jaarsveld, Richard H., Rafiullah, Rafiullah

المصدر: Cell Death & Disease; May2024, Vol. 15 Issue 5, p1-15, 15p

المؤلفون: Werren, Elizabeth A., LaForce, Geneva R., Srivastava, Anshika, Perillo, Delia R., Li, Shaokun, Johnson, Katherine, Baris, Safa, Berger, Brandon, Regan, Samantha L., Pfennig, Christian D., de Munnik, Sonja, Pfundt, Rolph, Hebbar, Malavika, Jimenez-Heredia, Raúl, Karakoc-Aydiner, Elif, Ozen, Ahmet, Dmytrus, Jasmin, Krolo, Ana, Corning, Ken, Prijoles, E. J.

المصدر: Nature Communications; 2/23/2024, Vol. 15 Issue 1, p1-21, 21p

مصطلحات موضوعية: INTELLECTUAL disabilities, RNA, DEVELOPMENTAL biology, NERVE tissue, GENETIC variation

المؤلفون: Werren, Elizabeth A., Srinivasan, Varunvenkat M., Gowda, Vykuntaraju K., Pandey, Akanksha, Vaish, Saurabh, Kabbur, Anusha Raj, Nandeesh, Bevinahalli N., Srivastava, Anshika

المصدر: American Journal of Medical Genetics. Part A; Sep2023, Vol. 191 Issue 9, p2446-2450, 5p

المؤلفون: Norton, Heather, Werren, Elizabeth, Friedlaender, Jonathan

مصطلحات موضوعية: Pigmentation phenotype, Natural selection, Island Melanesia

العلاقة: http://www.biomedcentral.com/1471-2156/16/122Test

الإتاحة: http://www.biomedcentral.com/1471-2156/16/122Test

المؤلفون: Norton, Heather L., Werren, Elizabeth, Friedlaender, Jonathan

المساهمون: University of Cincinnati (US)

المصدر: BMC Genetics ; volume 16, issue 1 ; ISSN 1471-2156

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1186/s12863-015-0277-xTest

المؤلفون: Werren, Elizabeth A., Garcia, Obed, Bigham, Abigail W.

المصدر: Human Genetics ; volume 140, issue 2, page 241-276 ; ISSN 0340-6717 1432-1203

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1007/s00439-020-02206-7Test

المؤلفون: Werren, Elizabeth A.^1,2 (AUTHOR), Garcia, Obed² (AUTHOR), Bigham, Abigail W.³ (AUTHOR) awbigham@ucla.edu

المصدر: Human Genetics. 2021, Vol. 140 Issue 2, p241-276. 36p.

مصطلحات موضوعية: *HUMAN biology, *HUMAN genetic variation, *GENETIC drift, *NATURAL selection, *HUMAN variation (Biology)

المؤلفون: Norton, Heather L., Edwards, Melissa, Krithika, S., Johnson, Monique, Werren, Elizabeth A., Parra, Esteban J.

مصطلحات موضوعية: psy, envir

العلاقة: https://arro.anglia.ac.uk/id/eprint/705734Test/

الإتاحة: https://arro.anglia.ac.uk/id/eprint/705734Test/