日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Measuring sexual dimorphism in human faces

测量人类面部的性别二态性

Da Silva, Cassidy; Hoskens, Hanne; Aponte, J David; Caine, Katherine; Weinberg, Seth M; Claes, Peter; Hallgrímsson, Benedikt

Laterality and Completeness Patterns of Nonsyndromic Clefts in a Multiethnic Cohort

多民族人群中非综合征性唇腭裂的侧别和完整性模式

Spencer, Christina; Machado-Paula, Ligiane A; Qian, Fang; Butali, Azeez; Buxo-Martinez, Carmen J; Padilla, Carmencita D; Restrepo-Muneton, Claudia; Valencia-Ramirez, Consuelo; Long, Ross E; Weinberg, Seth M; Marazita, Mary L; Murray, Jeff; Moreno Uribe, Lina M; Petrin, Aline L

The craniofacial shape of modern humans embodies genomic signatures of evolution, diversity, and clinical conditions

现代人类的颅面形态体现了进化、多样性和临床状况的基因组特征。

Goovaerts, Seppe; Devine, Jay; Claessens, Nina; Gabbita, Sameer; Deprest, Jolien; Pauwels, Kaat; Herrick, Noah; Mohammed, Jaaved; Mounier, Aurélien; Sofer, Tamar; Long, Hannah K; Bartsch, Ullrich; Hallgrímsson, Benedikt; Lewis, Sarah J; Richmond, Stephen; Bauermeister, Sarah; Walsh, Susan; Shaffer, John R; Shriver, Mark D; Naqvi, Sahin; Wysocka, Joanna; Kivisild, Toomas; Weinberg, Seth M; Claes, Peter

Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanation

7p14.1是唇腭裂风险位点吗?对多个群体拷贝数变异的全基因组研究既重复了之前的研究结果,也提供了一种新的解释。

Mukhopadhyay, Nandita; Feingold, Eleanor E; Brand, Harrison; Lee, Myoung Keun; Kurtas, Edibe Nehir; Sanchis-Juan, Alba; Moreno-Uribe, Lina; Wehby, George; Valencia-Ramirez, Luz Consuelo; Muñeton, Claudia P Restrepo; Padilla, Carmencita; Deleyiannis, Frederic; Poletta, Fernando A; Orioli, Ieda M; Hecht, Jacqueline T; Buxó, Carmen J; Butali, Azeez; Adeyemo, Wasiu L; Abebe, Mekonen Eshete; Vieira, Alexandre R; Shaffer, John R; Murray, Jeffrey C; Weinberg, Seth M; Ruczinski, Ingo; Leslie-Clarkson, Elizabeth J; Marazita, Mary L

Leveraging the genetics of human face shape boosts the discovery of orofacial cleft risk loci

利用人类面部形状的遗传学信息可以促进唇腭裂风险基因位点的发现。

Herrick, Noah; Goovaerts, Seppe; Manchel, Alexandra; Lee, Myoung Keun; Zhang, Xinyi; Davies, Amy; Carlson, Jenna C; Leslie-Clarkson, Elizabeth J; Lewis, Sarah J; Marazita, Mary L; Cotney, Justin; Claes, Peter; Shaffer, John R; Weinberg, Seth M

Trio-based GWAS reveals novel loci associated with different forms of isolated cleft lip

基于三联体的全基因组关联研究揭示了与不同类型孤立性唇裂相关的新基因位点

Herrick, Noah; Erdogan-Yildirim, Zeynep; Lee, Myoung Keun; Curtis, Sarah W; Berke, Seth; Brewer, Grace; McHenry, Toby; El Sergani, Ahmed M; Anderton, Joel; Mukhopadhyay, Nandita; Carlson, Jenna C; Beaty, Terri; Butali, Azeez; Buxo-Martinez, Carmen J; Hecht, Jacqueline T; Liao, Eric; Moreno Uribe, Lina M; Padilla, Carmencita D; Wehby, George; Feingold, Eleanor; Murray, Jeffrey C; Ruczinski, Ingo; Leslie-Clarkson, Elizabeth J; Weinberg, Seth M; Shaffer, John R; Marazita, Mary L

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios

通过分析818个三联体中改变蛋白质的新生变异,区分综合征型和非综合征型腭裂。

Robinson, Kelsey R; Curtis, Sarah W; Paschall, Justin E; Adeyemo, Wasiu Lanre; Beaty, Terri H; Butali, Azeez; Buxó, Carmen J; Cutler, David J; Epstein, Michael P; Gowans, Lord J J; Hecht, Jacqueline T; Shaw, Gary M; Uribe, Lina Moreno; Murray, Jeffrey C; Brand, Harrison; Weinberg, Seth M; Marazita, Mary L; Doheny, Kimberly F; Leslie-Clarkson, Elizabeth J

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

PRKCI 的罕见变异导致 Van der Woude 综合征和皮周病的其他特征

Robinson, Kelsey; Singh, Sunil K; Walkup, Rachel B; Fawwal, Dorelle V; Vilfort, Kendra M; Koloskee, Amanda; Fashina, Azeez; Adeyemo, Wasiu Lanre; Beaty, Terri H; Butali, Azeez; Buxó, Carmen J; Chung, Wendy K; Cutler, David J; Epstein, Michael P; Gasser, Brooklynn; Gowans, Lord J J; Hecht, Jacqueline T; Mankad, Anuj; Moreno Uribe, Lina; Scott, Daryl A; Shaw, Gary M; Thomas, Mary Ann; Weinberg, Seth M; Liao, Eric C; Brand, Harrison; Marazita, Mary L; Lipinski, Robert J; Murray, Jeffrey C; Cornell, Robert A; Leslie-Clarkson, Elizabeth J

Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variants

优化复杂形态特征的表型分析:增强常见和罕见遗传变异的发现

Yuan, Meng; Goovaerts, Seppe; Lee, Myoung K; Devine, Jay; Richmond, Stephen; Walsh, Susan; Shriver, Mark D; Shaffer, John R; Marazita, Mary L; Peeters, Hilde; Weinberg, Seth M; Claes, Peter

Enhanced insights into the genetic architecture of 3D cranial vault shape using pleiotropy-informed GWAS

利用多效性信息全基因组关联分析,加深对三维颅盖形态遗传结构的理解。

Goovaerts, Seppe; Naqvi, Sahin; Hoskens, Hanne; Herrick, Noah; Yuan, Meng; Shriver, Mark D; Shaffer, John R; Walsh, Susan; Weinberg, Seth M; Wysocka, Joanna; Claes, Peter