1. R. Michael Roberts 美国 University of Missouri 1996美国科学院院士;2002沃尔夫农业奖 Comparison of extravillous trophoblast cells derived from human embryonic stem cells and from first ..
2. Richard K. Miller 美国 Franklin W. Olin College of Engineering 2012美国工程院院士 Molecular pathways in placental-fetal development and disruption
3. Gleeson, Joseph G. 美国 University of California, San Diego 2013美国医学院院士 The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian child..
4. Mardis, Elaine R. 美国 Ohio State University College of Medicine and Public Health 2019美国医学院院士 Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy
5. Epstein, Jonathan A. 美国 University of Pennsylvania 2008美国医学院院士 Dysregulated H19/Igf2 expression disrupts cardiac-placental axis during development of Silver-Russel..
6. Marisa S. Bartolomei 美国 University of Pennsylvania 2021美国科学院院士 Dysregulated H19/Igf2 expression disrupts cardiac-placental axis during development of Silver-Russel..
7. Evan E. Eichler 美国 University of Washington 2012美国科学院院士;2017美国医学院院士 Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders
8. Muglia, Louis J. 美国 Burroughs Wellcome Fund 2013美国医学院院士 Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth
9. 王晓斌 美国 Johns Hopkins University 2018美国医学院院士 Association between atopic diseases and neurodevelopmental disabilities in a longitudinal birth coho..
10. Gibbs, Richard A. 美国 Baylor College of Medicine 2011美国医学院院士 Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome
11. Lupski, James R. 美国 Baylor College of Medicine 2002美国医学院院士 Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome
12. Richard P. Lifton 美国 The Rockefeller University 2001美国科学院院士;2002美国医学院院士 Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies a..
13. Hildebrandt, Friedhelm 美国 Harvard Medical School 2015美国医学院院士 Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies a..
14. Gleeson, Joseph G. 美国 University of California, San Diego 2013美国医学院院士 Sperm mosaicism: implications for genomic diversity and disease
15. Christopher A. Walsh 美国 Harvard University 2018美国科学院院士;2013美国医学院院士 RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes
16. Gibbs, Richard A. 美国 Baylor College of Medicine 2011美国医学院院士 RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes
17. Gleeson, Joseph G. 美国 University of California, San Diego 2013美国医学院院士 Closing in on Mechanisms of Open Neural Tube Defects
18. Christopher A. Walsh 美国 Harvard University 2018美国科学院院士;2013美国医学院院士 Duplication 2p16 is associated with perisylvian polymicrogyria
19. Gelb, Bruce D. 美国 Mount Sinai School of Medicine 2010美国医学院院士 Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart d..
20. Chung, Wendy K. 美国 Columbia University 2020美国医学院院士 Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN