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职业迁徙
个人简介
I have been conducting human genomics research for over 20 years. The highlights of my career are the discovery of the polymorphic Sp1 site in the COL1A1 gene and its association with osteoporosis, the identification of variation in the TCF7L2 gene playing a key role in conferring type 2 diabetes risk and providing leadership in an international genetics effort to characterize genes influencing birth weight and common childhood obesity risk. I have also previously played a role in uncovering genes involved in other traits, including cleft lip with or without palate, scoliosis, inflammatory bowel disease, autism, ADHD, head circumference, intracranial volume, myocardial infarction, pediatric eosinophilic esophagitis, type 1 diabetes, asthma, multiple sclerosis and neuroblastoma.
研究兴趣
论文共 408 篇作者统计合作学者相似作者
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Khanh B Trang,Matthew C Pahl,James A Pippin,Chun Su,Sheridan H Littleton,Prabhat Sharma, Nikhil N Kulkarni,Louis R Ghanem,Natalie A Terry, Joan M O'Brien,Yadav Wagley,Kurt D Hankenson,
medRxiv : the preprint server for health sciences (2024)
EBioMedicine (2024): 105038-105038
Sleep (2024)
eLife (2024)
Genome Biologyno. 1 (2024): 1-19
Nature Geneticsno. 7 (2023): 1250-1250
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Science Advancesno. 1 (2023)
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