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Genetic Variation in the Alternative Complement Pathway Contributes to Individual Susceptibility to Bacteremia and Sepsis Inman, Kyle; Chernus, Jonathan; Lee, Myoungkeun; Alder, Jonathan K.; Shah, Faraaz Ali; Mayr, Florian B.; Dempsey, Timothy; Nouraie, S. Mehdi; Dela Cruz, Charles; Ferreira, Viviana P.; Kulkarni, Hrishikesh S.; Meyer, Nuala J.; Strollo, Patrick J.; Feingold, Eleanor; Bain, William 分享 收藏
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk CALD1、ESRP1和RBFOX1的变异与面裂风险相关 Carlson, Jenna C.; Zhang, Xinyi; Erdogan-Yildirim, Zeynep; Beaty, Terri H.; Butali, Azeez; Buxo, Carmen J.; Gowans, Lord J. J.; Hecht, Jacqueline T.; Long, Ross E.; Moreno, Lina; Murray, Jeffrey C.; Orioli, Ieda M.; Padilla, Carmencita; Wehby, George L.; Feingold, Eleanor; Leslie-Clarkson, Elizabeth J.; Weinberg, Seth M.; Marazita, Mary L.; Shaffer, John R. 分享 收藏
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Search for the elusive haplotype of the APOE polymorphism associated with Alzheimer's disease 搜索与阿尔茨海默病相关的APOE多态性的难寻单倍型 Cheema, Asma Naseer; Fan, Kang-Hsien; Lawrence, Elizabeth; Zafari, Narges; Shi, Ruyu; Aslam, Muhammad Muaaz; Acharya, Vibha; Holderman, Alayna Jean; Bedison, Annie; Feingold, Eleanor 分享 收藏
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Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting Perez, Kimberly K. Diaz; Curtis, Sarah W.; Sanchis-Juan, Alba; Zhao, Xuefang; Head, Taylor; Ho, Samantha; Carter, Bridget; McHenry, Toby; Bishop, Madison R.; Valencia-Ramirez, Luz C.; Restrepo, Claudia; Hecht, Jacqueline T.; Uribe, Lina M.; Wehby, George; Weinberg, Seth M.; Beaty, Terri H.; Murray, Jeffrey C.; Feingold, Eleanor; Marazita, Mary L.; Cutler, David J.; Epstein, Michael P.; Brand, Harrison; Leslie, Elizabeth J. 分享 收藏
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Investigation of the independent role of a rare APOE variant (L28P; APOE*4Pittsburgh) in late-onset Alzheimer disease Fan, KangHsien; Francis, Lily; Aslam, M. Muaaz; Bedison, Margret A.; Lawrence, Elizabeth; Acharya, Vibha; Snitz, Beth E.; Ganguli, Mary; DeKosky, Steven T.; Lopez, Oscar L.; Feingold, Eleanor; Kamboh, M. Ilyas 分享 收藏
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Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations 东非人面部特征的基因组扫描和跨人群比较揭示了新的关联 Liu, Chenxing; Lee, Myoung Keun; Naqvi, Sahin; Hoskens, Hanne; Liu, Dongjing; White, Julie D.; Indencleef, Karlijne; Matthews, Harold; Eller, Ryan J.; Li, Jiarui; Mohammed, Jaaved; Swigut, Tomek; Richmond, Stephen; Manyama, Mange; Hallgrimsson, Benedikt; Spritz, Richard A.; Feingold, Eleanor; Marazita, Mary L.; Wysocka, Joanna; Walsh, Susan; Shriver, Mark D.; Claes, Peter; Weinberg, Seth M.; Shaffer, John R. 分享 收藏
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip 20p11的PAX1基因座是双侧唇裂的潜在遗传修饰因子 Curtis, Sarah W.; Chang, Daniel; Lee, Myoung Keun; Shaffer, John R.; Indencleef, Karlijne; Epstein, Michael P.; Cutler, David J.; Murray, Jeffrey C.; Feingold, Eleanor; Beaty, Terri H.; Claes, Peter; Weinberg, Seth M.; Marazita, Mary L.; Carlson, Jenna C.; Leslie, Elizabeth J. 分享 收藏
Impact of low-frequency coding variants on human facial shape 低频编码变体对人体面部形状的影响 Liu, Dongjing; Alhazmi, Nora; Matthews, Harold; Lee, Myoung Keun; Li, Jiarui; Hecht, Jacqueline T.; Wehby, George L.; Moreno, Lina M.; Heike, Carrie L.; Roosenboom, Jasmien; Feingold, Eleanor; Marazita, Mary L.; Claes, Peter; Liao, Eric C.; Weinberg, Seth M.; Shaffer, John R. 分享 收藏
Insights into the genetic architecture of the human face 洞察人脸的遗传结构 White, Julie D.; Indencleef, Karlijne; Naqvi, Sahin; Eller, Ryan J.; Hoskens, Hanne; Roosenboom, Jasmien; Lee, Myoung Keun; Li, Jiarui; Mohammed, Jaaved; Richmond, Stephen; Quillen, Ellen E.; Norton, Heather L.; Feingold, Eleanor; Swigut, Tomek; Marazita, Mary L.; Peeters, Hilde; Hens, Greet; Shaffer, John R.; Wysocka, Joanna; Walsh, Susan; Weinberg, Seth M.; Shriver, Mark D.; Claes, Peter 分享 收藏
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research Samuels, Bridget D.; Aho, Robert; Brinkley, James F.; Bugacov, Alejandro; Feingold, Eleanor; Fisher, Shannon; Gonzalez-Reiche, Ana S.; Hacia, Joseph G.; Hallgrimsson, Benedikt; Hansen, Karissa; Harris, Matthew P.; Thach-Vu Ho; Holmes, Greg; Hooper, Joan E.; Jabs, Ethylin Wang; Jones, Kenneth L.; Kesselman, Carl; Klein, Ophir D.; Leslie, Elizabeth J.; Li, Hong; Liao, Eric C.; Long, Hannah; Lu, Na; Maas, Richard L.; Marazita, Mary L.; Mohammed, Jaaved; Prescott, Sara; Schuler, Robert; Selleri, Licia; Spritz, Richard A.; Swigut, Tomek; van Bakel, Harm; Visel, Axel; Welsh, Ian; Williams, Cristina; Williams, Trevor J.; Wysocka, Joanna; Yuan, Yuan; Chai, Yang 分享 收藏
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Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios 口面裂三重奏中从头编码突变的全基因组富集 Bishop, Madison R.; Perez, Kimberly K. Diaz; Sun, Miranda; Ho, Samantha; Chopra, Pankaj; Mukhopadhyay, Nandita; Hetmanski, Jacqueline B.; Taub, Margaret A.; Moreno-Uribe, Lina M.; Valencia-Ramirez, Luz Consuelo; Restrepo Muneton, Claudia P.; Wehby, George; Hecht, Jacqueline T.; Deleyiannis, Frederic; Weinberg, Seth M.; Wu-Chou, Yah Huei; Chen, Philip K.; Brand, Harrison; Epstein, Michael P.; Ruczinski, Ingo; Murray, Jeffrey C.; Beaty, Terri H.; Feingold, Eleanor; Lipinski, Robert J.; Cutler, David J.; Marazita, Mary L.; Leslie, Elizabeth J. 分享 收藏
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21 来自Gabriella Miller儿童第一儿科研究联盟的口面裂三重奏的全基因组测序确定了21号染色体上的新基因座 Mukhopadhyay, Nandita; Bishop, Madison; Mortillo, Michael; Chopra, Pankaj; Hetmanski, Jacqueline B.; Taub, Margaret A.; Moreno, Lina M.; Consuelo Valencia-Ramirez, Luz; Restrepo, Claudia; Wehby, George L.; Hecht, Jacqueline T.; Deleyiannis, Frederic; Butali, Azeez; Weinberg, Seth M.; Beaty, Terri H.; Murray, Jefrey C.; Leslie, Elizabeth J.; Feingold, Eleanor; Marazita, Mary L. 分享 收藏
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