ScholarIQanswers from OpenAlex & ORCID
Sha Tang
ResearcherPublications, citations & collaboration network
Sha Tang is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Sha Tang have?
ScholarIQindexed works
Sha Tang has 199 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Sha Tang have?
ScholarIQcitation count
Sha Tang has 9,397 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Sha Tang?
ScholarIQh-index
Sha Tang has an h-index of 55 in OpenAlex.
What is the i10-index of Sha Tang?
ScholarIQi10-index
Sha Tang has an i10-index of 132 in OpenAlex.
What is the ORCID of Sha Tang?
ScholarIQorcid
The ORCID for Sha Tang is on the source record.
What is the OpenAlex record for Sha Tang?
ScholarIQopenalex
The OpenAlex for Sha Tang is on the source record.
What are the most-cited papers on Sha Tang?
ScholarIQmost cited works
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions
Kelly D. Farwell, Layla Shahmirzadi, Dima El‐Khechen, Zöe Powis, Elizabeth Chao, Brigette Tippin Davis, Ruth M. Baxter, Wenqi Zeng, Cameron Mroske, Melissa Parra, Stephanie Gandomi, Ira Lu, Xiang Li, Hong Lu, Hsiao‐Mei Lu, David Salvador, David Ruble, Monica Lao, Soren Fischbach, Jennifer X. Wen, Shela Lee, Aaron Elliott, Charles Dunlop, Sha Tang
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy
Katherine L. Helbig, Kelly D. Farwell Hagman, Deepali N. Shinde, Cameron Mroske, Zöe Powis, Shuwei Li, Sha Tang, Ingo Helbig
Genome-wide identification and functional prediction of novel and drought-responsive lincRNAs in Populus trichocarpa
Peng Shuai, Dan Liang, Sha Tang, Zhoujia Zhang, Chuyu Ye, Yanyan Su, Xinli Xia, Weilun Yin
De novo variants in neurodevelopmental disorders with epilepsy
Henrike Heyne, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Çağlayan, Dana Craiu, Peter De Jonghe, Renzo Guerrini, Katherine L. Helbig, Bobby P.C. Koeleman, Jack A. Kosmicki, Tarja Linnankivi, Patrick May, Hiltrud Muhle, Rikke S. Møller, Bernd A. Neubauer, Aarno Palotie, Manuela Pendziwiat, Pasquale Striano, Sha Tang, Sitao Wu, Annapurna Poduri, Yvonne Weber, Sarah Weckhuysen, Sanjay M. Sisodiya, Mark J. Daly, Ingo Helbig, Dennis Lal, Johannes R. Lemke
<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