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A neurogenetic analysis of female autism.
Published in:
2021
By:
- Jack, Allison;
- Sullivan, Catherine A W;
- Aylward, Elizabeth;
- Bookheimer, Susan Y;
- Dapretto, Mirella;
- Gaab, Nadine;
- Horn, John D Van;
- 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;
- Consortium, the GENDAAR;
- Van Horn, John D;
- GENDAAR Consortium
Publication type:
journal article
Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder.
Published in:
Frontiers in Psychiatry, 2021, v. 12, p. 1, doi. 10.3389/fpsyt.2021.716673
By:
- Enriquez, Kristen D.;
- Gupta, Abha R.;
- Hoffman, Ellen J.
Publication type:
Article
The relationship between gamma-band neural oscillations and language skills in youth with Autism Spectrum Disorder and their first-degree relatives.
Published in:
Molecular Autism, 2024, v. 15, n. 1, p. 1, doi. 10.1186/s13229-024-00598-1
By:
- 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
Publication type:
Article
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
Published in:
PLoS ONE, 2023, v. 18, n. 10, p. 1, doi. 10.1371/journal.pone.0291978
By:
- 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.
Publication type:
Article
Temporal and spatial regulation of gene expression mediated by the promoter for the human tissue inhibitor of metalloproteinases-3 (TIMP-3)-encoding gene.
Published in:
Developmental Dynamics, 1998, v. 211, n. 3, p. 228, doi. 10.1002/(SICI)1097-0177(199803)211:3<228::AID-AJA4>3.0.CO;2-J
By:
- Zeng, Yong;
- Rosborough, Rania C.;
- Li, Yanjiao;
- Gupta, Abha R.;
- Bennett, Jean
Publication type:
Article
PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2019, v. 12, n. 2, p. 200, doi. 10.1002/aur.2051
By:
- 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.
Publication type:
Article
Parenting Stress and its Associated Components Prior to an Autism Spectrum Disorder (ASD) Diagnostic Evaluation.
Published in:
Journal of Autism & Developmental Disorders, 2021, v. 51, n. 10, p. 3432, doi. 10.1007/s10803-020-04804-w
By:
- Voliovitch, Yair;
- Leventhal, John M.;
- Fenick, Ada M.;
- Gupta, Abha R.;
- Feinberg, Emily;
- Hickey, Emily J.;
- Shabanova, Veronika;
- Weitzman, Carol
Publication type:
Article
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 2, p. 165, doi. 10.1038/ejhg.2014.82
By:
- 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;
- Šestan, Nenad;
- State, Matthew W
Publication type:
Article
Basic fibroblast growth factor induces a transformed phenotype in normal human melanocytes.
Published in:
Oncogene, 1999, v. 18, n. 47, p. 6469, doi. 10.1038/sj.onc.1203066
By:
- Nesbit, Mark;
- Nesbit, Heike KE;
- Bennett, Jean;
- Andl, Thomas;
- Hsu, Mei-Yu;
- Dejesus, Emma;
- McBrian, Michelle;
- Gupta, Abha R;
- Eck, Stephen L;
- Herlyn, Meenhard
Publication type:
Article
Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.
Published in:
Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-31
By:
- Gupta, Abha R.;
- Pirruccello, Michelle;
- Feng Cheng;
- Hyo Jung Kang;
- Fernandez, Thomas V.;
- Baskin, Jeremy M.;
- Murim Choi;
- Li Liu;
- Ercan-Sencicek, Adife Gulhan;
- Murdoch, John D.;
- Klei, Lambertus;
- Neale, Benjamin M.;
- Franjic, Daniel;
- Daly, Mark J.;
- Lifton, Richard P.;
- De Camilli, Pietro;
- Hongyu Zhao;
- Šestan, Nenad;
- State, Matthew W.
Publication type:
Article
Strain-dependent anterior segment neovascularization following intravitreal gene transfer of basic fibroblast growth factor (bFGF).
Published in:
Journal of Gene Medicine, 2001, v. 3, n. 3, p. 252, doi. 10.1002/1521-2254(200105/06)3:3<252::AID-JGM185>3.0.CO;2-S
By:
- Gupta, Abha R.;
- Dejneka, Nadine S.;
- D'Amato, Robert J.;
- Yang, Zaixin;
- Syed, Nasreen;
- Maguire, Albert M.;
- Bennett, Jean
Publication type:
Article
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Published in:
Nature, 2012, v. 485, n. 7397, p. 237, doi. 10.1038/nature10945
By:
- 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.
Publication type:
Article
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.
Published in:
PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004852
By:
- 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.
Publication type:
Article
Identification of amygdala-expressed genes associated with autism spectrum disorder.
Published in:
Molecular Autism, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13229-020-00346-1
By:
- 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.
Publication type:
Article
Neurogenetic analysis of childhood disintegrative disorder.
Published in:
Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0133-0
By:
- 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
Publication type:
Article

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