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Eric M. Morrow

ResearcherPublications, citations & collaboration network

Eric M. Morrow is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Eric M. Morrow have?

ScholarIQindexed works

Eric M. Morrow has 149 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Eric M. Morrow have?

ScholarIQcitation count

Eric M. Morrow has 18,612 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Eric M. Morrow?

ScholarIQh-index

Eric M. Morrow has an h-index of 50 in OpenAlex.

What is the i10-index of Eric M. Morrow?

ScholarIQi10-index

Eric M. Morrow has an i10-index of 82 in OpenAlex.

What is the ORCID of Eric M. Morrow?

ScholarIQorcid

The ORCID for Eric M. Morrow is on the source record.

What is the OpenAlex record for Eric M. Morrow?

ScholarIQopenalex

The OpenAlex for Eric M. Morrow is on the source record.

What are the most-cited papers on Eric M. Morrow?

ScholarIQmost cited works
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An, Minshi Peng, Ryan L. Collins, Jakob Grove, Lambertus Klei, Christine Stevens, Jennifer Reichert, Maureen Mulhern, Mykyta Artomov, Sherif Gerges, Brooke Sheppard, Xinyi Xu, Aparna Bhaduri, Utku Norman, Harrison Brand, Grace Schwartz, Rachel Nguyen, Elizabeth E. Guerrero, Caroline Dias, Branko Aleksić, Richard Anney, Mafalda Barbosa, Somer Bishop, Alfredo Brusco, Jonas Bybjerg‐Grauholm, Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montse Fernández‐Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, Alexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Morgana Silva Montenegro, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura
Cell. 20202,488 CitationsOPEN ACCESS
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan Sanders, Xin He, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Kaitlin E. Samocha, A. Ercüment Çiçek, Michael T. Murtha, Vanessa H. Bal, Somer Bishop, Shan Dong, Arthur P. Goldberg, Jinlu Cai, John F. Keaney, Lambertus Klei, Jeffrey D. Mandell, Daniel Moreno‐De‐Luca, Christopher S. Poultney, Elise Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y. Su, Nicole A. Teran, Michael F. Walker, Donna M. Werling, Arthur L. Beaudet, Rita M. Cantor, Éric Fombonne, Daniel H. Geschwind, Dorothy E. Grice, Catherine Lord, Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State
Neuron. 20151,561 CitationsOPEN ACCESS
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State
Neuron. 20111,300 CitationsOPEN ACCESS
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
Brett S. Abrahams, Dan E. Arking, Jerry L. Campbell, Heather C. Mefford, Eric M. Morrow, Lauren A. Weiss, Idan Menashe, Tim Wadkins, Sharmila Banerjee‐Basu, Alan Packer
Molecular Autism. 2013955 CitationsOPEN ACCESS
Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders
Michael S. Ching, Yiping Shen, Wen‐Hann Tan, Shafali Jeste, Eric M. Morrow, Xiaoli Chen, Nahit Motavallı Mukaddes, Seung‐Yun Yoo, Ellen Hanson, Rachel J. Hundley, Christina L. Austin, Ronald E. Becker, Gerard T. Berry, Katherine Driscoll, Elizabeth C. Engle, Sandra Friedman, James F. Gusella, Fuki M. Hisama, Mira Irons, Tina Lafiosca, Elaine LeClair, David T. Miller, Michael Neessen, Jonathan Picker, Leonard Rappaport, Cynthia M. Rooney, Dean Sarco, Joan M. Stoler, Christopher A. Walsh, Robert R. Wolff, Ting Zhang, Ramzi H. Nasir, Bai‐Lin Wu
American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 2010311 CitationsOPEN ACCESS

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