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T

Tess Levy

Icahn School of Medicine at Mount Sinai
H指数:19
被引数:2,929

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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
2026-03-300
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
Catatonia in Autism and Neurodevelopmental Disorders: A Scoping Review for Advancing Identification, Practice, and Research

自闭症和神经发育障碍中的紧张症：一项旨在推进识别、实践和研究的范围综述

journal of the american academy of child & adolescent psychiatry
IF0
2026-03-250
OAAI
Pilar Trelles; Tess Levy; Sonal Jain; Bonnie Lerman; Kate Friedman; Wendy K. Chung; Kelli C. Dominick; Kacie Dunham-Carr; Martine Lamy; April R. Levin; James Luccarelli; Ryan O'Connor; Chase Samsel; Joshua R. Smith; Siddharth Srivastava; Audrey Thurm; Matthew Siegel
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
2025-10-180
PRE
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
Protein-truncating variants and deletions of SHANK2 are associated with autism spectrum disorder and other neurodevelopmental concerns

蛋白截短变异和SHANK2的缺失与自闭症谱系障碍及其他神经发育问题相关。

JOURNAL OF NEURODEVELOPMENTAL DISORDERS
IF4
2025-04-300
OA
Silver, Hailey; Greenberg, Rori; Siper, Paige M.; Zweifach, Jessica; Soufer, Renee; Sahin, Mustafa; Berry-Kravis, Elizabeth; Soorya, Latha Valluripalli; Thurm, Audrey; Bernstein, Jonathan A.; Kolevzon, Alexander; Grice, Dorothy E.; Buxbaum, Joseph D.; Levy, Tess
Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome

Phelan-McDermid综合征癫痫发作的临床、遗传和认知相关性

JOURNAL OF NEURODEVELOPMENTAL DISORDERS
IF4
2024-05-100
OAAI
Levy, Tess; Gluckman, Jacob; Siper, Paige M.; Halpern, Danielle; Zweifach, Jessica; Filip-Dhima, Rajna; Holder Jr, J. Lloyd; Trelles, M. Pilar; Johnson, Kristina; Bernstein, Jonathan A.; Berry-Kravis, Elizabeth; Powell, Craig M.; Soorya, Latha Valluripalli; Thurm, Audrey; Buxbaum, Joseph D.; Sahin, Mustafa; Kolevzon, Alexander; Srivastava, Siddharth
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
2023-06-0111
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
Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome

Phelan-McDermid综合征中的大22 q13.3缺失干扰外周转录组和代谢组学谱

HUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
2023-01-014
OAAI
Breen, Michael S.; Fan, Xuanjia; Levy, Tess; Pollak, Rebecca M.; Collins, Brett; Osman, Aya; Tocheva, Anna S.; Sahin, Mustafa; Berry-Kravis, Elizabeth; Soorya, Latha; Thurm, Audrey; Powell, Craig M.; Bernstein, Jonathan A.; Kolevzon, Alexander; Buxbaum, Joseph D.
An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome
HUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
2022-10-0112
OAAI
Kolevzon, Alexander; Levy, Tess; Barkley, Sarah; Bedrosian-Sermone, Sandra; Davis, Matthew; Foss-Feig, Jennifer; Halpern, Danielle; Keller, Katherine; Kostic, Ana; Layton, Christina; Lee, Rebecca; Lerman, Bonnie; Might, Matthew; Sandin, Sven; Siper, Paige M.; Sloofman, Laura G.; Walker, Hannah; Zweifach, Jessica; Buxbaum, Joseph D.
Neurodevelopmental copy-number variants: A roadmap to improving outcomes by uniting patient advocates, researchers, and clinicians for collective impact
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2022-08-019
OAAI
Buttermore, Elizabeth; Chamberlain, Stormy; Cody, Jannine; Costain, Gregory; Dang, Louis; DeWoody, Andrew; DeWoody, Yssa; Dies, Kira; Eichler, Evan; Girirajan, Santhosh; Gramm, Marie; Halladay, Alycia; Lal, Dennis; Lalli, Matthew; Levy, Tess; Logsdon, Glennis; Lowenstein, Daniel; Mefford, Heather; Mulle, Jennifer; Muotri, Alysson; Murphy, Melissa; Palma, Eduardo Perez; Pinter, Stefan; Pollak, Rebecca; Purcell, Ryan; Samaco, Rodney; Shah, Bina; Singh, Karun; So, Joyce; Sundberg, Maria; Veeraragavan, Surabi; Vogel-Farley, Vanessa; Wynshaw-Boris, Anthony

研究方向

暂未获取到该数据
J
Joseph D. Buxbaum
H 指数:140论文数:796被引数:11.8万
A
Alexander Kolevzon
H 指数:51论文数:225被引数:1.9万
P
Paige M. Siper
H 指数:26论文数:93被引数:5,201
D
Danielle Halpern
H 指数:20论文数:46被引数:4,381
J
Jessica Zweifach
H 指数:11论文数:25被引数:674
J
Jennifer H. Foss‐Feig
H 指数:34论文数:119被引数:5,142
B
Bonnie Lerman
H 指数:7论文数:14被引数:241
A
Audrey Thurm
H 指数:58论文数:301被引数:1.5万
E
Elizabeth Berry‐Kravis
H 指数:90论文数:553被引数:2.7万
S
Silvia De Rubeis
H 指数:40论文数:129被引数:1.7万