ScholarIQanswers from OpenAlex & ORCID
Elaine H. Zackai
ResearcherPublications, citations & collaboration network
Elaine H. Zackai is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Elaine H. Zackai have?
ScholarIQindexed works
Elaine H. Zackai has 1,077 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Elaine H. Zackai have?
ScholarIQcitation count
Elaine H. Zackai has 50,221 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Elaine H. Zackai?
ScholarIQh-index
Elaine H. Zackai has an h-index of 113 in OpenAlex.
What is the i10-index of Elaine H. Zackai?
ScholarIQi10-index
Elaine H. Zackai has an i10-index of 545 in OpenAlex.
What is the ORCID of Elaine H. Zackai?
ScholarIQorcid
The ORCID for Elaine H. Zackai is on the source record.
What is the OpenAlex record for Elaine H. Zackai?
ScholarIQopenalex
The OpenAlex for Elaine H. Zackai is on the source record.
What are the most-cited papers on Elaine H. Zackai?
ScholarIQmost cited works
Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
Maude Schneider, Martin Debbané, Anne S. Bassett, Eva W.C. Chow, Wai Lun Alan Fung, Marianne B. M. van den Bree, Michael J. Owen, Kieran C. Murphy, Maria Niarchou, Wendy R. Kates, Kevin M. Antshel, Wanda Fremont, Donna M. McDonald‐McGinn, Raquel E. Gur, Elaine H. Zackai, Jacob Vorstman, Sasja N. Duijff, Petra Klaassen, Ann Swillen, Doron Gothelf, Tamar Green, Abraham Weizman, Thérèse van Amelsvoort, L. J. M. Evers, Erik Boot, Vandana Shashi, Stephen R. Hooper, Carrie E. Bearden, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Declan Murphy, Opal Ousley, Linda Campbell, Tony J. Simon, Stéphan Eliez
Characterization of Potocki-Lupski Syndrome (dup(17)(p11.2p11.2)) and Delineation of a Dosage-Sensitive Critical Interval That Can Convey an Autism Phenotype
Lorraine Potocki, Weimin Bi, Diane Treadwell‐Deering, Claudia M.B. Carvalho, Anna Eifert, Ellen M. Friedman, Daniel G. Glaze, Kevin R. Krull, Jennifer A. Lee, Richard A. Lewis, Roberto Mendoza‐Londono, Patricia Robbins‐Furman, Chad A. Shaw, Xin Shi, George Weissenberger, Marjorie Withers, Svetlana A. Yatsenko, Elaine H. Zackai, Paweł Stankiewicz, James R. Lupski
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
Konrad Platzer, Hongjie Yuan, Hannah M. Schutz, Alexander Winschel, Wenjuan Chen, Chun Hu, Hirofumi Kusumoto, Henrike Heyne, Katherine L. Helbig, Sha Tang, Marcia Willing, Brad T. Tinkle, Darius J. Adams, Christel Depienne, Boris Keren, Cyril Mignot, Eirik Frengen, Petter Strømme, Saskia Biskup, Dennis Döcker, Tim M. Strom, Heather C. Mefford, Candace T. Myers, Alison M. Muir, Amy Lacroix, Lynette G. Sadleir, Ingrid E. Scheffer, Eva H. Brilstra, Mieke M. van Haelst, Jasper J. van der Smagt, Levinus A. Bok, Rikke S. Møller, Uffe Birk Jensen, J Gordon Millichap, Anne T. Berg, Ethan M. Goldberg, Isabelle De Bie, Stéphanie Fox, Philippe Major, Julie R. Jones, Elaine H. Zackai, Rami Abou Jamra, Arndt Rolfs, Richard J. Leventer, John A. Lawson, Tony Roscioli, Floor E. Jansen, Emmanuelle Ranza, Christian Korff, Anna-Elina Lehesjoki, Carolina Courage, Tarja Linnankivi, Douglas R Smith, Christine M. Stanley, Mark Mintz, Dianalee McKnight, Amy Decker, Wen‐Hann Tan, Mark A. Tarnopolsky, Lauren Brady, Markus Wolff, Lutz Dondit, Hélio Pedro, Sarah Parisotto, Kelly L. Jones, Anup D. Patel, David Neal Franz, Rena Vanzo, Elysa Marco, Judith D. Ranells, Nataliya Di Donato, William B. Dobyns, Bodo Laube, Stephen F. Traynelis, Johannes R. Lemke
Human Chromosome 7: DNA Sequence and Biology
Stephen W. Scherer, Joseph Cheung, Jeffrey R. MacDonald, Lucy R. Osborne, Kazuhiko Nakabayashi, Jo-Anne Herbrick, Andrew R. Carson, Layla Parker-Katiraee, Jennifer Skaug, Razi Khaja, Junjun Zhang, Alexander K. Hudek, Martin Li, May Hobeika Haddad, Gavin E. Duggan, Bridget A. Fernandez, Emiko Kanematsu, S. Gentles, Constantine Christopoulos, Sanaa Choufani, Dorota A. Kwasnicka, Xiangqun Zheng-Bradley, Zhongwu Lai, Deborah Nusskern, Qing Zhang, Zhiping Gu, Fu Lu, Susan Zeesman, Małgorzata J.M. Nowaczyk, Ikuko Teshima, David Chitayat, Cheryl Shuman, Rosanna Weksberg, Elaine H. Zackai, Theresa A. Grebe, Sarah Cox, Susan J. Kirkpatrick, Nazneen Rahman, Jan M. Friedman, Henry H. Heng, Pier Giuseppe Pelicci, Francesco Lo‐Coco, Elena Belloni, Lisa G. Shaffer, Barbara R. Pober, Cynthia C. Morton, James F. Gusella, G.A.P. Bruns, Bruce R. Korf, Bradley J. Quade, Azra H. Ligon, Heather Ferguson, Anne W. Higgins, Natalia T. Leach, Steven R. Herrick, Emmanuelle Lemyre, Chantal G. Farra, Hyung‐Goo Kim, Anne Summers, Karen W. Gripp, Wendy Roberts, Péter Szatmári, E.J.T. Winsor, Karl‐Heinz Grzeschik, Ahmed Teebi, Berge A. Minassian, Juha Kere, Lluı́s Armengol, Miguel Ángel Pujana, Xavier Estivill, Michael D. Wilson, Ben F. Koop, Sabrina Tosi, Gudrun E. Moore, Andrew P. Boright, Eitan Zlotorynski, Batsheva Kerem, Peter M. Kroisel, Erwin Petek, David Oscier, Sarah Mould, Hartmut DoÌhner, Konstanze DoÌhner, Johanna M. Rommens, John B. Vincent, J. Craig Venter, Peter W. Li, Richard Mural, Mark D. Adams, Lap-Chee Tsui
Spectrum of <i>MLL2</i> (<i>ALR</i>) mutations in 110 cases of Kabuki syndrome
Mark Hannibal, Kati J. Buckingham, Sarah Ng, Jeffrey E. Ming, Anita E. Beck, Margaret J. McMillin, Heidi Gildersleeve, Abigail W. Bigham, Holly K. Tabor, Heather C. Mefford, Joseph Cook, Koh‐ichiro Yoshiura, Tadashi Matsumoto, Naomichi Matsumoto, Noriko Miyake, Hidefumi Tonoki, Kenji Naritomi, Tadashi Kaname, Toshiro Nagai, Hirofumi Ohashi, Kenji Kurosawa, Jia‐Woei Hou, Tohru Ohta, Deshung Liang, Akira Sudo, Colleen A. Morris, Siddharth Banka, Graeme C. Black, Jill Clayton‐Smith, Deborah A. Nickerson, Elaine H. Zackai, Tamim H. Shaikh, Dian Donnai, Norio Niikawa, Jay Shendure, Michael J. Bamshad