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Jeremy Schwartzentruber

ResearcherPublications, citations & collaboration network

Jeremy Schwartzentruber is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Jeremy Schwartzentruber have?

ScholarIQindexed works

Jeremy Schwartzentruber has 178 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Jeremy Schwartzentruber have?

ScholarIQcitation count

Jeremy Schwartzentruber has 22,545 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Jeremy Schwartzentruber?

ScholarIQh-index

Jeremy Schwartzentruber has an h-index of 64 in OpenAlex.

What is the i10-index of Jeremy Schwartzentruber?

ScholarIQi10-index

Jeremy Schwartzentruber has an i10-index of 122 in OpenAlex.

What is the ORCID of Jeremy Schwartzentruber?

ScholarIQorcid

The ORCID for Jeremy Schwartzentruber is on the source record.

What is the OpenAlex record for Jeremy Schwartzentruber?

ScholarIQopenalex

The OpenAlex for Jeremy Schwartzentruber is on the source record.

What are the most-cited papers on Jeremy Schwartzentruber?

ScholarIQmost cited works
Mapping the human genetic architecture of COVID-19
COVID-19 Host Genetics Initiative, COVID-19 Host Genetics InitiativeLeadership, Mari Niemi, Juha Karjalainen, Rachel G. Liao, Benjamin M. Neale, Mark J. Daly, Andrea Ganna, Writing group, Writing group leaders, Gita A. Pathak, Shea J. Andrews, Masahiro Kanai, Writing group members, Kumar Veerapen, Israel Fernández‐Cadenas, Eva C. Schulte, Pasquale Striano, M. Marttila, Camelia C. Minică, Eirini Marouli, Mohd Anisul Karim, Frank R. Wendt, Jeanne E. Savage, Laura Sloofman, Guillaume Butler‐Laporte, Han‐Na Kim, Stavroula Kanoni, Yukinori Okada, Jinyoung Byun, Younghun Han, Mohammed Jashim Uddin, George Davey Smith, Cristen J. Willer, Joseph D. Buxbaum, Analysis group, Manuscript analyses team leader, Manuscript analyses team member: meta-analysis, Juha Mehtonen, Manuscript analyses team member: heritability, methods and supplements, Manuscript analyses team member: PHEWAS, Manuscript analyses team member: Mendelian randomization, Manuscript analyses team member: PC projection and gene prioritization, Manuscript analyses team member: gene prioritization, Hilary K. Finucane, Manuscript analyses team member: sensitivity analysis, Mattia Cordioli, Manuscript analyses team members: PC projection, Alicia R. Martin, Wei Zhou, In silico analysis team members, Bogdan Paşaniuc, Hanna Julienne, Hugues Aschard, Huwenbo Shi, Loïc Yengo, Renato Polimanti, Maya Ghoussaini, Jeremy Schwartzentruber, Ian Dunham, Project management group, Project management leader, Project management support, Karolina Chwiałkowska, Margherita Francescatto, Amy Trankiem, Mary K. Balaconis, Phenotype steering group, Lea K. Davis, Sulggi A. Lee, James R. Priest, Alessandra Renieri, Vijay G. Sankaran, David A. van Heel, Patrick Deelen, J. Brent Richards, Tomoko Nakanishi, Les Biesecker, V. Eric Kerchberger, J. Kenneth Baillie, Data dictionary, Francesca Mari, Anna Bernasconi, J. Kenneth Baillie, Arif Canakoglu, Scientific communication group, Scientific communication leaders, Brooke Wolford, Scientific communication members, Annika Faucon, Atanu Kumar Dutta, Claudia Schurmann, Emi N. Harry, Ewan Birney, Huy Nguyen, Jamal Nasir, Mari Kaunisto, Matthew Solomonson, Nicole Dueker, Nirmal Vadgama
Nature. 20211,122 CitationsOPEN ACCESS
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
Adam M. Fontebasso, Simon Papillon‐Cavanagh, Jeremy Schwartzentruber, Hamid Nikbakht, Noha Gerges, Pierre Fiset, Denise Béchet, Damien Faury, Nicolas Jay, Lori Ramkissoon, Aoife Corcoran, David Jones, Dominik Sturm, Pascal D. Johann, Tadanori Tomita, Stewart Goldman, Mahmoud G. Nagib, Anne Bendel, Liliana Goumnerova, Daniel C. Bowers, Jeffrey R Leonard, Joshua B. Rubin, Tord D. Alden, Samuel R. Browd, J. Russell Geyer, Sarah Leary, George I. Jallo, Kenneth J. Cohen, Nalin Gupta, Michael D. Prados, Anne‐Sophie Carret, Benjamin Ellezam, Louis Crevier, Álmos Klekner, László Bognár, Péter Hauser, Miklós Garami, John S. Myseros, Zhifeng Dong, Peter M. Siegel, Hayley Malkin, Azra H. Ligon, Steffen Albrecht, Stefan M. Pfister, Keith L. Ligon, Jacek Majewski, Nada Jabado, Mark W. Kieran
Nature Genetics. 2014472 CitationsOPEN ACCESS
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
Robert K. Koenekoop, Hui Wang, Jacek Majewski, Xia Wang, Irma López, Huanan Ren, Yiyun Chen, Yumei Li, Gerald A. Fishman, Mohammed Genead, Jeremy Schwartzentruber, Naimesh Solanki, Elias I. Traboulsi, Jingliang Cheng, Clare V. Logan, Martin McKibbin, Bruce E. Hayward, David Parry, Colin A. Johnson, Mohammed Nageeb, James A. Poulter, Moin Mohamed, Hussain Jafri, Yasmin Abdul Rashid, Graham R. Taylor, Vafa Keser, Graeme Mardon, Huidan Xu, Chris F. Inglehearn, Qing Fu, Carmel Toomes, Rui Chen
Nature Genetics. 2012207 Citations

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