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1.

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

Willsey, A Jeremy; Sanders, Stephan J; Li, Mingfeng; Dong, Shan; Tebbenkamp, Andrew T; Muhle, Rebecca A; Reilly, Steven K; Lin, Leon; Fertuzinhos, Sofia; Miller, Jeremy A; Murtha, Michael T; Bichsel, Candace; Niu, Wei; Cotney, Justin; Ercan-Sencicek, A Gulhan; Gockley, Jake; Gupta, Abha R; Han, Wenqi; He, Xin; Hoffman, Ellen J; Klei, Lambertus; Lei, Jing; Liu, Wenzhong; Liu, Li; Lu, Cong; Xu, Xuming; Zhu, Ying; Mane, Shrikant M; Lein, Ed S; Wei, Liping; Noonan, James P; Roeder, Kathryn; Devlin, Bernie; Sestan, Nenad; State, Matthew W.

Cell ; 155(5): 997-1007, 2013 Nov 21.

Article in English | MEDLINE | ID: mdl-24267886

2.

A neurogenetic analysis of female autism.

Jack, Allison; Sullivan, Catherine A W; Aylward, Elizabeth; Bookheimer, Susan Y; Dapretto, Mirella; Gaab, Nadine; Van Horn, John D; Eilbott, Jeffrey; Jacokes, Zachary; Torgerson, Carinna M; Bernier, Raphael A; Geschwind, Daniel H; McPartland, James C; Nelson, Charles A; Webb, Sara J; Pelphrey, Kevin A; Gupta, Abha R.

Brain ; 144(6): 1911-1926, 2021 07 28.

Article in English | MEDLINE | ID: mdl-33860292

3.

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.

Sanders, Stephan J; Murtha, Michael T; Gupta, Abha R; Murdoch, John D; Raubeson, Melanie J; Willsey, A Jeremy; Ercan-Sencicek, A Gulhan; DiLullo, Nicholas M; Parikshak, Neelroop N; Stein, Jason L; Walker, Michael F; Ober, Gordon T; Teran, Nicole A; Song, Youeun; El-Fishawy, Paul; Murtha, Ryan C; Choi, Murim; Overton, John D; Bjornson, Robert D; Carriero, Nicholas J; Meyer, Kyle A; Bilguvar, Kaya; Mane, Shrikant M; Sestan, Nenad; Lifton, Richard P; Günel, Murat; Roeder, Kathryn; Geschwind, Daniel H; Devlin, Bernie; State, Matthew W.

Nature ; 485(7397): 237-41, 2012 Apr 04.

Article in English | MEDLINE | ID: mdl-22495306

4.

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.

Murdoch, John D; Gupta, Abha R; Sanders, Stephan J; Walker, Michael F; Keaney, John; Fernandez, Thomas V; Murtha, Michael T; Anyanwu, Samuel; Ober, Gordon T; Raubeson, Melanie J; DiLullo, Nicholas M; Villa, Natalie; Waqar, Zainabdul; Sullivan, Catherine; Gonzalez, Luis; Willsey, A Jeremy; Choe, So-Yeon; Neale, Benjamin M; Daly, Mark J; State, Matthew W.

PLoS Genet ; 11(1): e1004852, 2015 Jan.

Article in English | MEDLINE | ID: mdl-25621974

5.

The relationship between gamma-band neural oscillations and language skills in youth with Autism Spectrum Disorder and their first-degree relatives.

Arutiunian, Vardan; Santhosh, Megha; Neuhaus, Emily; Borland, Heather; Tompkins, Chris; Bernier, Raphael A; Bookheimer, Susan Y; Dapretto, Mirella; Gupta, Abha R; Jack, Allison; Jeste, Shafali; McPartland, James C; Naples, Adam; Van Horn, John D; Pelphrey, Kevin A; Webb, Sara Jane.

Mol Autism ; 15(1): 19, 2024 May 07.

Article in English | MEDLINE | ID: mdl-38711098

6.

Copy Number Variation Informs fMRI-based Prediction of Autism Spectrum Disorder.

Dvornek, Nicha C; Sullivan, Catherine; Duncan, James S; Gupta, Abha R.

Mach Learn Clin Neuroimaging (2023) ; 14312: 133-142, 2023 Oct.

Article in English | MEDLINE | ID: mdl-38371906

7.

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.

Fernandez, Thomas V; Williams, Zsanett P; Kline, Tina; Rajendran, Shreenath; Augustine, Farhan; Wright, Nicole; Sullivan, Catherine A W; Olfson, Emily; Abdallah, Sarah B; Liu, Wenzhong; Hoffman, Ellen J; Gupta, Abha R; Singer, Harvey S.

PLoS One ; 18(10): e0291978, 2023.

Article in English | MEDLINE | ID: mdl-37788244

8.

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Bakkaloglu, Betul; O'Roak, Brian J; Louvi, Angeliki; Gupta, Abha R; Abelson, Jesse F; Morgan, Thomas M; Chawarska, Katarzyna; Klin, Ami; Ercan-Sencicek, A Gulhan; Stillman, Althea A; Tanriover, Gamze; Abrahams, Brett S; Duvall, Jackie A; Robbins, Elissa M; Geschwind, Daniel H; Biederer, Thomas; Gunel, Murat; Lifton, Richard P; State, Matthew W.

Am J Hum Genet ; 82(1): 165-73, 2008 Jan.

Article in English | MEDLINE | ID: mdl-18179895

9.

Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder.

Enriquez, Kristen D; Gupta, Abha R; Hoffman, Ellen J.

Front Psychiatry ; 12: 716673, 2021.

Article in English | MEDLINE | ID: mdl-34690830

10.

Sex-dependent role for EPHB2 in brain development and autism-associated behavior.

Assali, Ahlem; Cho, Jennifer Y; Tsvetkov, Evgeny; Gupta, Abha R; Cowan, Christopher W.

Neuropsychopharmacology ; 46(11): 2021-2029, 2021 10.

Article in English | MEDLINE | ID: mdl-33649502

11.

Parenting Stress and its Associated Components Prior to an Autism Spectrum Disorder (ASD) Diagnostic Evaluation.

Voliovitch, Yair; Leventhal, John M; Fenick, Ada M; Gupta, Abha R; Feinberg, Emily; Hickey, Emily J; Shabanova, Veronika; Weitzman, Carol.

J Autism Dev Disord ; 51(10): 3432-3442, 2021 Oct.

Article in English | MEDLINE | ID: mdl-33387245

12.

Engineering spatial-organized cardiac organoids for developmental toxicity testing.

Hoang, Plansky; Kowalczewski, Andrew; Sun, Shiyang; Winston, Tackla S; Archilla, Adriana M; Lemus, Stephanie M; Ercan-Sencicek, A Gulhan; Gupta, Abha R; Liu, Wenzhong; Kontaridis, Maria I; Amack, Jeffrey D; Ma, Zhen.

Stem Cell Reports ; 16(5): 1228-1244, 2021 05 11.

Article in English | MEDLINE | ID: mdl-33891865

13.

Identification of amygdala-expressed genes associated with autism spectrum disorder.

Herrero, Maria Jesus; Velmeshev, Dmitry; Hernandez-Pineda, David; Sethi, Saarthak; Sorrells, Shawn; Banerjee, Payal; Sullivan, Catherine; Gupta, Abha R; Kriegstein, Arnold R; Corbin, Joshua G.

Mol Autism ; 11(1): 39, 2020 05 27.

Article in English | MEDLINE | ID: mdl-32460837

14.

De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.

Cappi, Carolina; Oliphant, Melody E; Péter, Zsanett; Zai, Gwyneth; Conceição do Rosário, Maria; Sullivan, Catherine A W; Gupta, Abha R; Hoffman, Ellen J; Virdee, Manmeet; Olfson, Emily; Abdallah, Sarah B; Willsey, A Jeremy; Shavitt, Roseli G; Miguel, Euripedes C; Kennedy, James L; Richter, Margaret A; Fernandez, Thomas V.

Biol Psychiatry ; 87(12): 1035-1044, 2020 06 15.

Article in English | MEDLINE | ID: mdl-31771860

15.

PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder.

Goodrich, Meredith; Armour, Anna Chelsea; Panchapakesan, Karuna; You, Xiaozhen; Devaney, Joseph; Knoblach, Susan; Sullivan, Catherine A W; Herrero, Maria Jesus; Gupta, Abha R; Vaidya, Chandan J; Kenworthy, Lauren; Corbin, Joshua G.

Autism Res ; 12(2): 200-211, 2019 02.

Article in English | MEDLINE | ID: mdl-30556326

16.

Recent advances in the genetics of autism.

Gupta, Abha R; State, Matthew W.

Biol Psychiatry ; 61(4): 429-37, 2007 Feb 15.

Article in English | MEDLINE | ID: mdl-16996486

17.

Neurogenetic analysis of childhood disintegrative disorder.

Gupta, Abha R; Westphal, Alexander; Yang, Daniel Y J; Sullivan, Catherine A W; Eilbott, Jeffrey; Zaidi, Samir; Voos, Avery; Vander Wyk, Brent C; Ventola, Pam; Waqar, Zainulabedin; Fernandez, Thomas V; Ercan-Sencicek, A Gulhan; Walker, Michael F; Choi, Murim; Schneider, Allison; Hedderly, Tammy; Baird, Gillian; Friedman, Hannah; Cordeaux, Cara; Ristow, Alexandra; Shic, Frederick; Volkmar, Fred R; Pelphrey, Kevin A.

Mol Autism ; 8: 19, 2017.

Article in English | MEDLINE | ID: mdl-28392909

18.

[Autism: genetics]. / Autismo: genética.

Gupta, Abha R; State, Matthew W.

Braz J Psychiatry ; 28 Suppl 1: S29-38, 2006 May.

Article in Portuguese | MEDLINE | ID: mdl-16791389

19.

Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.

Ercan-Sencicek, A Gulhan; Jambi, Samira; Franjic, Daniel; Nishimura, Sayoko; Li, Mingfeng; El-Fishawy, Paul; Morgan, Thomas M; Sanders, Stephan J; Bilguvar, Kaya; Suri, Mohnish; Johnson, Michele H; Gupta, Abha R; Yuksel, Zafer; Mane, Shrikant; Grigorenko, Elena; Picciotto, Marina; Alberts, Arthur S; Gunel, Murat; Sestan, Nenad; State, Matthew W.

Eur J Hum Genet ; 23(2): 165-72, 2015 Feb.

Article in English | MEDLINE | ID: mdl-24781755

20.

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

Gupta, Abha R; Pirruccello, Michelle; Cheng, Feng; Kang, Hyo Jung; Fernandez, Thomas V; Baskin, Jeremy M; Choi, Murim; Liu, Li; Ercan-Sencicek, Adife Gulhan; Murdoch, John D; Klei, Lambertus; Neale, Benjamin M; Franjic, Daniel; Daly, Mark J; Lifton, Richard P; De Camilli, Pietro; Zhao, Hongyu; Sestan, Nenad; State, Matthew W.

Mol Autism ; 5: 31, 2014.

Article in English | MEDLINE | ID: mdl-24860643

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