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Mark W. Kieran

ResearcherPublications, citations & collaboration network

Mark W. Kieran is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Mark W. Kieran have?

ScholarIQindexed works

Mark W. Kieran has 558 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Mark W. Kieran have?

ScholarIQcitation count

Mark W. Kieran has 31,232 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Mark W. Kieran?

ScholarIQh-index

Mark W. Kieran has an h-index of 93 in OpenAlex.

What is the i10-index of Mark W. Kieran?

ScholarIQi10-index

Mark W. Kieran has an i10-index of 272 in OpenAlex.

What is the ORCID of Mark W. Kieran?

ScholarIQorcid

The ORCID for Mark W. Kieran is on the source record.

What is the OpenAlex record for Mark W. Kieran?

ScholarIQopenalex

The OpenAlex for Mark W. Kieran is on the source record.

What are the most-cited papers on Mark W. Kieran?

ScholarIQmost cited works
A small-molecule antagonist of CXCR4 inhibits intracranial growth of primary brain tumors
Joshua B. Rubin, Andrew L. Kung, Robyn S. Klein, Jennifer A. Chan, Yanping Sun, Karl Schmidt, Mark W. Kieran, Andrew D. Luster, Rosalind A. Segal
Proceedings of the National Academy of Sciences. 2003612 CitationsOPEN ACCESS
Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas
Priscilla K. Brastianos, Amaro Taylor‐Weiner, Peter Manley, Robert T. Jones, Dora Dias‐Santagata, Aaron R. Thorner, Michael S. Lawrence, Fausto J. Rodríguez, Lindsay A. Bernardo, Laura Schubert, Ashwini Sunkavalli, Nick Shillingford, Monica L. Calicchio, Hart G.W. Lidov, Hala Taha, Maria Martinez‐Lage, Mariarita Santi, Phillip B. Storm, John Y. K. Lee, James N. Palmer, Nithin D. Adappa, R. Michael Scott, Ian F. Dunn, Edward R. Laws, Chip Stewart, Keith L. Ligon, Mai P. Hoang, Paul Van Hummelen, William C. Hahn, David N. Louis, Adam Resnick, Mark W. Kieran, Gad Getz, Sandro Santagata
Nature Genetics. 2014518 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

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