Nicholas A. Watts - Publications, H-index & Citations

Nicholas A. Watts

Broad Institute of MIT and Harvard

23H指数

51论文数

1.7W被引数

收录论文 7

发表时间

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database 探索基因组聚合数据库中超过80万人的临床相关变异的穿透性

Nature Communications

IF15.7

2025-10-31

OAAI

Sanna Gudmundsson; Moriel Singer-Berk; Sarah L. Stenton; Julia K. Goodrich; Michael W. Wilson; Jonah Einson; Nicholas A. Watts; Tuuli Lappalainen; Heidi L. Rehm; Daniel G. MacArthur; Anne O’Donnell-Luria

Improved allele frequencies in gnomAD through local ancestry inference 通过局部祖先推断在gnomAD中改进等位基因频率

Nature Communications

IF15.7

2025-10-06

OAAI

Pragati Kore; Michael W. Wilson; Grace Tiao; Katherine Chao; Philip W. Darnowsky; Nicholas A. Watts; Jessica Honorato Mauer; Samantha M. Baxter; Heidi L. Rehm; Mark J. Daly; Konrad J. Karczewski; Elizabeth G. Atkinson

Advanced variant classification framework reduces the false positive rate of predicted loss-of-function variants in population sequencing data

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-09-01

OAAI

Singer-Berk, Moriel; Gudmundsson, Sanna; Baxter, Samantha; Seaby, Eleanor G.; England, Eleina; Wood, Jordan C.; Son, Rachel G.; Watts, Nicholas A.; Karczewski, Konrad J.; Harrison, Steven M.; Macarthur, Daniel G.; Rehm, Heidi L.; O'Donnell-Luria, Anne

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

CELL GENOMICS

IF9

2022-09-01

OAAI

Karczewski, Konrad J.; Solomonson, Matthew; Chao, Katherine R.; Goodrich, Julia K.; Tiao, Grace; Lu, Wenhan; Riley-Gillis, Bridget M.; Tsai, Ellen A.; Kim, Hye In; Zheng, Xiuwen; Rahimov, Fedik; Esmaeeli, Sahar; Grundstad, A. Jason; Reppell, Mark; Waring, Jeff; Jacob, Howard; Sexton, David; Bronson, Paola G.; Chen, Xing; Hu, Xinli; Goldstein, Jacqueline I.; King, Daniel; Vittal, Christopher; Poterba, Timothy; Palmer, Duncan S.; Churchhouse, Claire; Howrigan, Daniel P.; Zhou, Wei; Watts, Nicholas A.; Nguyen, Kevin; Nguyen, Huy; Mason, Cara; Farnham, Christopher; Tolonen, Charlotte; Gauthier, Laura D.; Gupta, Namrata; MacArthur, Daniel G.; Rehm, Heidi L.; Seed, Cotton; Philippakis, Anthony A.; Daly, Mark J.; Davis, J. Wade; Runz, Heiko; Miller, Melissa R.; Neale, Benjamin M.

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia 双相情感障碍中的外显子组测序将AKAP11鉴定为与精神分裂症共享的风险基因

NATURE GENETICS

IF31.8

2022-04-11

OAAI

Palmer, Duncan S.; Howrigan, Daniel P.; Chapman, Sinead B.; Adolfsson, Rolf; Bass, Nick; Blackwood, Douglas; Boks, Marco P. M.; Chen, Chia-Yen; Churchhouse, Claire; Corvin, Aiden P.; Craddock, Nicholas; Curtis, David; Di Florio, Arianna; Dickerson, Faith; Freimer, Nelson B.; Goes, Fernando S.; Jia, Xiaoming; Jones, Ian; Jones, Lisa; Jonsson, Lina; Kahn, Rene S.; Landen, Mikael; Locke, Adam E.; McIntosh, Andrew M.; McQuillin, Andrew; Morris, Derek W.; O'Donovan, Michael C.; Ophoff, Roel A.; Owen, Michael J.; Pedersen, Nancy L.; Posthuma, Danielle; Reif, Andreas; Risch, Neil; Schaefer, Catherine; Scott, Laura; Singh, Tarjinder; Smoller, Jordan W.; Solomonson, Matthew; St Clair, David; Stahl, Eli A.; Vreeker, Annabel; Walters, James T. R.; Wang, Weiqing; Watts, Nicholas A.; Yolken, Robert; Zandi, Peter P.; Neale, Benjamin M.

Mitochondrial DNA variation across 56,434 individuals in gnomAD

GENOME RESEARCH

IF5.5

2022-01-24

OAAI

Laricchia, Kristen M.; Lake, Nicole J.; Watts, Nicholas A.; Shand, Megan; Haessly, Andrea; Gauthier, Laura; Benjamin, David; Banks, Eric; Soto, Jose; Garimella, Kiran; Emery, James; Rehm, Heidi L.; MacArthur, Daniel G.; Tiao, Grace; Lek, Monkol; Mootha, Vamsi K.; Calvo, Sarah E.

Variant interpretation using population databases: Lessons from gnomAD 使用人口数据库的变体解释: gnomAD的经验教训

HUMAN MUTATION

IF3.7

2021-12-16

302

OAAI

Gudmundsson, Sanna; Singer-Berk, Moriel; Watts, Nicholas A.; Phu, William; Goodrich, Julia K.; Solomonson, Matthew; Rehm, Heidi L.; MacArthur, Daniel G.; O'Donnell-Luria, Anne

研究方向