F. Kyle Satterstrom - Publications, H-index & Citations

F. Kyle Satterstrom

mount sinai

39H指数

105论文数

1.7W被引数

收录论文 41

发表时间

Identification of moderate effect size genes in autism spectrum disorder through a novel gene pairing approach 通过新型基因配对方法鉴定自闭症谱系障碍中的中等效应量基因

Communications Biology

IF5.1

2026-05-30

OAAI

Madison Caballero; F. Kyle Satterstrom; Silvia de Rubeis; Joseph D. Buxbaum; Behrang Mahjani

Deleterious coding variation associated with autism is shared across ancestries 与自闭症相关的有害编码变异在祖先之间共享

Nature Medicine

IF50

2026-03-30

OAAI

Marina Natividad Avila; Seulgi Jung; F. Kyle Satterstrom; Jack M. Fu; Tess Levy; Laura G. Sloofman; Lambertus Klei; Thariana Pichardo; Dalia Marquez; Christine R. Stevens; Caroline M. Cusick; Jennifer L. Ames; Gabriele S. Campos; Hilda Cerros; Roberto Chaskel; Claudia I. S. Costa; Michael L. Cuccaro; Andrea del Pilar Lopez; Magdalena Fernandez; Eugenio Ferro; Liliana Galeano; Ana Cristina D. E. S. Girardi; Anthony J. Griswold; Luis C. Hernandez; Naila Lourenço; Yunin Ludena; Diana Núñez-Ríos; Rosa Oyama; Katherine P. Peña; Isaac Pessah; Rebecca Schmidt; Holly M. Sweeney; Lizbeth Tolentino; Jaqueline Y. T. Wang; Lilia Albores-Gallo; Lisa A. Croen; Carlos S. Cruz-Fuentes; Irva Hertz-Picciotto; Alexander Kolevzon; Maria Claudia Lattig; Liliana Mayo; Maria Rita Passos-Bueno; Margaret A. Pericak-Vance; Paige M. Siper; Flora Tassone; M. Pilar Trelles; Michael E. Talkowski; Mark J. Daly; Behrang Mahjani; Silvia De Rubeis; Edwin H. Cook; Kathryn Roeder; Catalina Betancur; Bernie Devlin; Joseph D. Buxbaum

MIRAGE: A Bayesian statistical method for gene-level rare-variant analysis incorporating functional annotations MIRAGE：一种整合功能注释的基因水平稀有变异分析的贝叶斯统计方法

The American Journal of Human Genetics

IF0

2025-12-19

PREAI

Shengtong Han; Xiaotong Sun; Laura Sloofman; F. Kyle Satterstrom; Xizhi Xu; Lifan Liang; Nicholas Knoblauch; Wenhui Sheng; Siming Zhao; Tan-Hoang Nguyen; Gao Wang; Joseph Buxbaum; Xin He

Rare genetic variants confer a high risk of ADHD and implicate neuronal biology 稀有遗传变异会增加ADHD的风险，并涉及神经元生物学。

Nature

IF48.5

2025-11-12

OAAI

Ditte Demontis; Jinjie Duan; Yu-Han H. Hsu; Greta Pintacuda; Jakob Grove; Trine Tollerup Nielsen; Janne Thirstrup; Makayla Martorana; Travis Botts; F. Kyle Satterstrom; Jonas Bybjerg-Grauholm; Jason H. Y. Tsai; Simon Glerup; Martine Hoogman; Jan Buitelaar; Marieke Klein; Georg C. Ziegler; Christian Jacob; Oliver Grimm; Maximilian Bayas; Nene F. Kobayashi; Sarah Kittel-Schneider; Klaus-Peter Lesch; Barbara Franke; Andreas Reif; Esben Agerbo; Thomas Werge; Merete Nordentoft; Ole Mors; Preben Bo Mortensen; Kasper Lage; Mark J. Daly; Benjamin M. Neale; Anders D. Børglum

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder KDM6B相关的神经发育障碍的临床与分子谱

The American Journal of Human Genetics

IF0

2025-10-18

PREAI

Dmitrijs Rots; Taryn E. Jakub; Crystal Keung; Adam Jackson; Siddharth Banka; Rolph Pfundt; Bert B.A. de Vries; Richard H. van Jaarsveld; Saskia M.J. Hopman; Ellen van Binsbergen; Irene Valenzuela; Maja Hempel; Tatjana Bierhals; Fanny Kortüm; Francois Lecoquierre; Alice Goldenberg; Jens Michael Hertz; Charlotte Brasch Andersen; Maria Kibæk; Eloise J. Prijoles; Roger E. Stevenson; David B. Everman; Wesley G. Patterson; Linyan Meng; Charul Gijavanekar; Karl De Dios; Shenela Lakhani; Tess Levy; Matias Wagner; Dagmar Wieczorek; Paul J. Benke; María Soledad Lopez Garcia; Renee Perrier; Sergio B. Sousa; Pedro M. Almeida; Maria José Simões; Bertrand Isidor; Wallid Deb; Andrew A. Schmanski; Omar Abdul-Rahman; Christophe Philippe; Ange-Line Bruel; Laurence Faivre; Antonio Vitobello; Christel Thauvin; Jeroen J. Smits; Livia Garavelli; Stefano G. Caraffi; Francesca Peluso; Laura Davis-Keppen; Dylan Platt; Erin Royer; Lisette Leeuwen; Margje Sinnema; Alexander P.A. Stegmann; Constance T.R.M. Stumpel; George E. Tiller; Daniëlle G.M. Bosch; Stephanus T. Potgieter; Shelagh Joss; Miranda Splitt; Simon Holden; Matina Prapa; Nicola Foulds; Sofia Douzgou; Kaija Puura; Regina Waltes; Andreas G. Chiocchetti; Christine M. Freitag; F. Kyle Satterstrom; Silvia De Rubeis; Joseph Buxbaum; Bruce D. Gelb; Aleksic Branko; Itaru Kushima; Jennifer Howe; Stephen W. Scherer; Alessia Arado; Chiara Baldo; Olivier Patat; Demeer Bénédicte; Diego Lopergolo; Filippo M. Santorelli; Tobias B. Haack; Andreas Dufke; Miriam Bertrand; Ruth J. Falb; Angelika Rieß; Peter Krieg; Stephanie Spranger; Maria Francesca Bedeschi; Maria Iascone; Sarah Josephi-Taylor; Tony Roscioli; Michael F. Buckley; Jan Liebelt; Aditi I. Dagli; Emmelien Aten; Anna C.E. Hurst; Alesha Hicks; Mohnish Suri; Ermal Aliu; Sunil Naik; Richard Sidlow; Juliette Coursimault; Gaël Nicolas; Hanna Küpper; Florence Petit; Veyan Ibrahim; Deniz Top; Francesca Di Cara; Raymond J. Louie; Elliot Stolerman; Han G. Brunner; Lisenka E.L.M. Vissers; Jamie M. Kramer; Tjitske Kleefstra

Contribution of autosomal rare and de novo variants to sex differences in autism

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2025-02-01

OAAI

Koko, Mahmoud; Satterstrom, F. Kyle; Warrier, Varun; Martin, Hilary

THE ALLELIC ARCHITECTURE OF RARE VARIATION IN AUTISM AND OTHER NEURODEVELOPMENTAL CONDITIONS

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2024-10-01

PREAI

Fu, Jack; Satterstrom, F. Kyle; McWalter, Kirsty; Brand, Harrison; Kueffner, Robert; Cutler, David; Samocha, Kaitlin; Robinson, Elise; Buxbaum, Joseph; Devlin, Bernie; Roeder, Kathryn; Kruszka, Paul; Sanders, Stephan; Daly, Mark; Talkowski, Michael

CHARACTERIZING FUNCTIONAL CONVERGENCE OF COMMON POLYGENIC VARIATION IN NEUROPSYCHIATRIC DISORDER RISK GENES

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2024-10-01

PREAI

Kuo, Susan; Weiner, Daniel; Ling, Emi; Fu, Jack; Satterstrom, F. Kyle; Talkowski, Michael; McCarroll, Steve; Robinson, Elise

HOW MUCH DO RARE DE NOVO VARIANTS CONTRIBUTE TO AUTISM?

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2024-10-01

PREAI

Nadig, Ajay; Lu, Wenhan; Fu, Jack; Satterstrom, F. Kyle; Karczewski, Konrad; Talkowski, Michael; Robinson, Elise; O'Connor, Luke

CROSS-DISORDER RARE VARIANT ANALYSIS OF AUTISM AND ADHD

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2024-10-01

PREAI

Duan, Jinjie; Grove, Jakob; Demontis, Ditte; Satterstrom, F. Kyle; Fu, Jack; Carey, Caitlin; Sanders, Stephan; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph; Robinson, Elise; Talkowski, Michael; Neale, Benjamin; Daly, Mark; Borglum, Anders

THE POLYGENETIC ARCHITECTURE OF AUTISM

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2024-10-01

PREAI

Zhang, Jing; Grove, Jakob; Carey, Caitlin; Fu, Jack; Satterstrom, F. Kyle; Kuo, Susan; Nadig, Ajay; Awasthi, Swapnil; Samocha, Kaitlin; Borglum, Anders; Robinson, Elise

CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE VARIANTS: INSIGHTS FROM DANISH IPSYCH EXOMES

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2023-10-01

PREAI

Duan, Jinjie; Grove, Jakob; Demontis, Ditte; Satterstrom, F. Kyle; Fu, Jack; Carey, Caitlin; Sanders, Stephan J.; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph; Robinson, Elise; Talkowski, Michael; Neale, Benjamin; Daly, Mark; Borglum, Anders

Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders

NATURE GENETICS

IF31.8

2023-07-27

OAAI

Valencia, Alfredo M.; Sankar, Akshay; van der Sluijs, Pleuntje J.; Satterstrom, F. Kyle; Fu, Jack; Talkowski, Michael E.; Vergano, Samantha A. Schrier; Santen, Gijs W. E.; Kadoch, Cigall

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder KDM6B-related神经发育障碍的临床和分子谱

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-06-01

OAAI

Rots, Dmitrijs; Jakub, Taryn E.; Keung, Crystal; Lisenka, Vissers E. L. M.; Banka, Siddharth; Pfundt, Rolph; de Vries, Bert B. A.; van Jaarsveld, Richard H.; Hopman, Saskia M. J.; van Binsbergen, Ellen; Valenzuela, Irene; Hempel, Maja; Bierhals, Tatjana; Kortuem, Fanny; Lecoquierre, Francois; Goldenberg, Alice; Hertz, Jens Michael; Andersen, Charlotte Brasch; Kibaek, Maria; Prijoles, Eloise J.; Stevenson, Roger E.; Everman, David B.; Patterson, Wesley G.; Meng, Linyan; Gijavanekar, Charul; De Dios, Karl; Lakhani, Shenela; Levy, Tess; Wagner, Matias; Wieczorek, Dagmar; Benke, Paul J.; Garcia, Maria Soledad Lopez; Perrier, Renee; Sousa, Sergio B.; Almeida, Pedro M.; Simoes, Maria Jose; Isidor, Bertrand; Deb, Wallid; Schmanski, Andrew A.; Abdul-Rahman, Omar; Philippe, Christophe; Bruel, Ange-Line; Faivre, Laurence; Vitobello, Antonio; Thauvin, Christel; Smits, Jeroen J.; Garavelli, Livia; Caraffi, Stefano G.; Peluso, Francesca; Davis-Keppen, Laura; Platt, Dylan; Royer, Erin; Leeuwen, Lisette; Sinnema, Margje; Stegmann, Alexander P. A.; Stumpel, Constance T. R. M.; Tiller, George E.; Bosch, Danielle G. M.; Potgieter, Stephanus T.; Joss, Shelagh; Splitt, Miranda; Holden, Simon; Prapa, Matina; Foulds, Nicola; Douzgou, Sofia; Puura, Kaija; Waltes, Regina; Chiocchetti, Andreas G.; Freitag, Christine M.; Satterstrom, F. Kyle; De Rubeis, Silvia; Buxbaum, Joseph; Gelb, Bruce D.; Branko, Aleksic; Kushima, Itaru; Howe, Jennifer; Scherer, Stephen W.; Arado, Alessia; Baldo, Chiara; Patat, Olivier; Benedicte, Demeer; Lopergolo, Diego; Santorelli, Filippo M.; Haack, Tobias B.; Dufke, Andreas; Bertrand, Miriam; Falb, Ruth J.; Riess, Angelika; Krieg, Peter; Spranger, Stephanie; Bedeschi, Maria Francesca; Iascone, Maria; Josephi-Taylor, Sarah; Roscioli, Tony; Buckley, Michael F.; Liebelt, Jan; Dagli, Aditi I.; Aten, Emmelien; Hurst, Anna C. E.; Hicks, Alesha; Suri, Mohnish; Aliu, Ermal; Naik, Sunil; Sidlow, Richard; Coursimault, Juliette; Nicolas, Gael; Kuepper, Hanna; Petit, Florence; Ibrahim, Veyan; Top, Deniz; Di Cara, Francesca; Louie, Raymond J.; Stolerman, Elliot; Brunner, Han G.; Vissers, Lisenka E. L. M.; Kramer, Jamie M.; Kleefstra, Tjitske

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains (vol 55, pg 198, 2023)

NATURE GENETICS

IF31.8

2023-03-01

OAAI

Demontis, Ditte; Walters, G. Bragi; Athanasiadis, Georgios; Walters, Raymond; Therrien, Karen; Nielsen, Trine Tollerup; Farajzadeh, Leila; Voloudakis, Georgios; Bendl, Jaroslav; Zeng, Biau; Zhang, Wen; Grove, Jakob; Als, Thomas D.; Duan, Jinjie; Satterstrom, F. Kyle; Bybjerg-Grauholm, Jonas; Baekved-Hansen, Marie H.; Gudmundsson, Olafur; Magnusson, Sigurdur; Baldursson, Gisli; Davidsdottir, Katrin C.; Haraldsdottir, Gyda; Agerbo, Esben; Hoffman, Gabriel M.; Dalsgaard, Soren; Martin, Jonna; Ribases, Marta; Boomsma, Dorret H.; Soler Artigas, Maria; Roth Mota, Nina; Howrigan, Daniel; Medland, Sarah J.; Zayats, Tetyana J.; Rajagopal, Veera; Nordentoft, Merete; Mors, Ole; Hougaard, David M.; Mortensen, Preben Bo; Daly, Mark J.; Faraone, Stephen V.; Stefansson, Hreinn; Roussos, Panos; Franke, Barbara; Werge, Thomas; Neale, Benjamin M.; Stefansson, Kari; Borglum, Anders D.

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains ADHD的全基因组分析确定了27个风险位点，完善了遗传结构并暗示了几个认知域

NATURE GENETICS

IF31.8

2023-01-26

192

OAAI

Demontis, Ditte; Walters, G. Bragi; Athanasiadis, Georgios; Walters, Raymond; Therrien, Karen; Nielsen, Trine Tollerup; Farajzadeh, Leila; Voloudakis, Georgios; Bendl, Jaroslav; Zeng, Biau; Zhang, Wen; Grove, Jakob; Als, Thomas D.; Duan, Jinjie; Satterstrom, F. Kyle; Bybjerg-Grauholm, Jonas; Baekved-Hansen, Marie; Gudmundsson, Olafur O.; Magnusson, Sigurdur H.; Baldursson, Gisli; Davidsdottir, Katrin; Haraldsdottir, Gyda S.; Agerbo, Esben; Hoffman, Gabriel E.; Dalsgaard, Soren; Martin, Joanna; Ribases, Marta; Boomsma, Dorret, I; Artigas, Maria Soler; Mota, Nina Roth; Howrigan, Daniel; Medland, Sarah E.; Zayats, Tetyana; Rajagopal, Veera M.; Nordentoft, Merete; Mors, Ole; Hougaard, David M.; Mortensen, Preben Bo; Daly, Mark J.; Faraone, Stephen, V; Stefansson, Hreinn; Roussos, Panos; Franke, Barbara; Werge, Thomas; Neale, Benjamin M.; Stefansson, Kari; Borglum, Anders D.

ANALYSIS OF RARE CODING AND COMMON VARIANTS IN AUTISM AND COMORBID SUBGROUPS

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2022-10-01

PREAI

Duan, Jinjie; Grove, Jakob; Satterstrom, F. Kyle; Fu, Jack; Carey, Caitlin; Wang, Jiebiao; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph; Robinson, Elise; Talkowski, Michael; Daly, Mark; Borglum, Anders

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism 罕见的编码变异提供了对自闭症遗传结构和表型背景的洞察

NATURE GENETICS

IF31.8

2022-08-18

198

OAAI

Fu, Jack M.; Satterstrom, F. Kyle; Peng, Minshi; Brand, Harrison; Collins, Ryan L.; Dong, Shan; Wamsley, Brie; Klei, Lambertus; Wang, Lily; Hao, Stephanie P.; Stevens, Christine R.; Cusick, Caroline; Babadi, Mehrtash; Banks, Eric; Collins, Brett; Dodge, Sheila; Gabriel, Stacey B.; Gauthier, Laura; Lee, Samuel K.; Liang, Lindsay; Ljungdahl, Alicia; Mahjani, Behrang; Sloofman, Laura; Smirnov, Andrey N.; Barbosa, Mafalda; Betancur, Catalina; Brusco, Alfredo; Chung, Brian H. Y.; Cook, Edwin H.; Cuccaro, Michael L.; Domenici, Enrico; Ferrero, Giovanni Battista; Gargus, J. Jay; Herman, Gail E.; Hertz-Picciotto, Irva; Maciel, Patricia; Manoach, Dara S.; Passos-Bueno, Maria Rita; Persico, Antonio M.; Renieri, Alessandra; Sutcliffe, James S.; Tassone, Flora; Trabetti, Elisabetta; Campos, Gabriele; Cardaropoli, Simona; Carli, Diana; Chan, Marcus C. Y.; Fallerini, Chiara; Giorgio, Elisa; Girardi, Ana Cristina; Hansen-Kiss, Emily; Lee, So Lun; Lintas, Carla; Ludena, Yunin; Nguyen, Rachel; Pavinato, Lisa; Pericak-Vance, Margaret; Pessah, Isaac N.; Schmidt, Rebecca J.; Smith, Moyra; Costa, Claudia I. S.; Trajkova, Slavica; Wang, Jaqueline Y. T.; Yu, Mullin H. C.; Cutler, David J.; De Rubeis, Silvia; Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Roeder, Kathryn; Sanders, Stephan J.; Talkowski, Michael E.

Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder

NATURE GENETICS

IF31.8

2022-08-04

OAAI

Rajagopal, Veera M.; Duan, Jinjie; Vilar-Ribo, Laura; Grove, Jakob; Zayats, Tetyana; Antoni Ramos-Quiroga, J.; Satterstrom, F. Kyle; Soler Artigas, Maria; Bybjerg-Grauholm, Jonas; Baekvad-Hansen, Marie; Als, Thomas D.; Rosengren, Anders; Daly, Mark J.; Neale, Benjamin M.; Nordentoft, Merete; Werge, Thomas; Mors, Ole; Hougaard, David M.; Mortensen, Preben B.; Ribases, Marta; Borglum, Anders D.; Demontis, Ditte

The female protective effect against autism spectrum disorder

CELL GENOMICS

IF9

2022-06-01

OAAI

Wigdor, Emilie M.; Weiner, Daniel J.; Grovo, Jako; Fu, Jack M.; Thompson, Wesley K.; Carey, Caitlin E.; Baya, Nikolas; van der Merwe, Celia; Walters, Raymond K.; Satterstrom, F. Kyle; Palmer, Duncan S.; Rosengren, Anders; iPSYCH Consortium, David M.; Hougaard, David M.; Mortensen, Preben Bo; Daily, Mark J.; Talkowski, Michael E.; Sanders, Stephan J.; Bishop, Somer L.; Borglum, Anders D.; Robinson, Elise B.

研究方向