Evin M. Padhi - Publications, H-index & Citations

Evin M. Padhi

stanford university

9H指数

23论文数

364被引数

收录论文 5

发表时间

Genomics-Informed Approach Identifies Which Cell Types Regulate the Metabolome 基因组学指导的方法鉴定调控代谢组的细胞类型

Bioinformatics

IF5.4

2026-05-29

OAAI

Haim Krupkin; Evin M Padhi; Daniel Nachun; Jessica Kain; Jonathan Z Long; Stephen B Montgomery; null

Transcriptome-wide outlier approach identifies individuals with minor spliceopathies 转录组范围离群值方法识别具有微小剪接病变的个体

american journal of human genetics

IF0

2025-09-19

OAAI

Taylor M. Arriaga; Rodrigo Mendez; Rachel A. Ungar; Devon E. Bonner; Dena R. Matalon; Gabrielle Lemire; Pagé C. Goddard; Evin M. Padhi; Alexander M. Miller; Jonathan V. Nguyen; Jialan Ma; Kevin S. Smith; Stuart A. Scott; Linda Liao; Zena Ng; Shruti Marwaha; Guney Bademci; Stephanie A. Bivona; Mustafa Tekin; Jonathan A. Bernstein; Stephen B. Montgomery; Anne O’Donnell-Luria; Matthew T. Wheeler; Vijay S. Ganesh

Predicting expression-altering promoter mutations with deep learning 利用深度学习预测改变表达量的启动子突变

Science

IF45.8

2025-05-29

PREAI

Kishore Jaganathan; Nicole Ersaro; Gherman Novakovsky; Yuchuan Wang; Terena James; Jeremy Schwartzentruber; Petko Fiziev; Irfahan Kassam; Fan Cao; Johann Hawe; Henry Cavanagh; Ashley Lim; Grace Png; Jeremy McRae; Abhimanyu Banerjee; Arvind Kumar; Jacob Ulirsch; Yan Zhang; Francois Aguet; Pierrick Wainschtein; Laksshman Sundaram; Adriana Salcedo; Sofia Kyriazopoulou Panagiotopoulou; Delasa Aghamirzaie; Evin Padhi; Ziming Weng; Shan Dong; Damian Smedley; Mark Caulfield; Anne O’Donnell-Luria; Heidi L. Rehm; Stephan J. Sanders; Anshul Kundaje; Stephen B. Montgomery; Mark T. Ross; Kyle Kai-How Farh

de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project de novo变体调用在1000基因组项目中识别癌症突变特征

HUMAN MUTATION

IF3.7

2022-09-10

OAAI

Ng, Jeffrey K.; Vats, Pankaj; Fritz-Waters, Elyn; Sarkar, Stephanie; Sams, Eleanor I.; Padhi, Evin M.; Payne, Zachary L.; Leonard, Shawn; West, Marc A.; Prince, Chandler; Trani, Lee; Jansen, Marshall; Vacek, George; Samadi, Mehrzad; Harkins, Timothy T.; Pohl, Craig; Turner, Tychele N.

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

HUMAN GENOMICS

IF4.3

2021-07-13

OAAI

Padhi, Evin M.; Hayeck, Tristan J.; Cheng, Zhang; Chatterjee, Sumantra; Mannion, Brandon J.; Byrska-Bishop, Marta; Willems, Marjolaine; Pinson, Lucile; Redon, Sylvia; Benech, Caroline; Uguen, Kevin; Audebert-Bellanger, Severine; Le Marechal, Cedric; Ferec, Claude; Efthymiou, Stephanie; Rahman, Fatima; Maqbool, Shazia; Maroofian, Reza; Houlden, Henry; Musunuri, Rajeeva; Narzisi, Giuseppe; Abhyankar, Avinash; Hunter, Riana D.; Akiyama, Jennifer; Fries, Lauren E.; Ng, Jeffrey K.; Mehinovic, Elvisa; Stong, Nick; Allen, Andrew S.; Dickel, Diane E.; Bernier, Raphael A.; Gorkin, David U.; Pennacchio, Len A.; Zody, Michael C.; Turner, Tychele N.

研究方向