ScholarIQanswers from OpenAlex & ORCID
David N. Louis
ResearcherPublications, citations & collaboration network
David N. Louis is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does David N. Louis have?
ScholarIQindexed works
David N. Louis has 628 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does David N. Louis have?
ScholarIQcitation count
David N. Louis has 143,793 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of David N. Louis?
ScholarIQh-index
David N. Louis has an h-index of 137 in OpenAlex.
What is the i10-index of David N. Louis?
ScholarIQi10-index
David N. Louis has an i10-index of 354 in OpenAlex.
What is the ORCID of David N. Louis?
ScholarIQorcid
The ORCID for David N. Louis is on the source record.
What is the OpenAlex record for David N. Louis?
ScholarIQopenalex
The OpenAlex for David N. Louis is on the source record.
What are the most-cited papers on David N. Louis?
ScholarIQmost cited works
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
Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1)
Trilochan Sahoo, Eric W. Johnson, James W. Thomas, Peter Kuehl, Tamara L. Jones, C. G. Dokken, Jeffrey W. Touchman, Carol J. Gallione, S.-Q. Lee-Lin, Barry E. Kosofsky, Janice Kurth, David N. Louis, Gabrielle Mettler, Leslie Morrison, António Gil‐Nagel, Stephen S. Rich, Joseph M. Zabramski, Mark S. Boguski, Eric D. Green, Douglas A. Marchuk
<i>Maternally Expressed Gene 3</i>, an Imprinted Noncoding RNA Gene, Is Associated with Meningioma Pathogenesis and Progression
Xun Zhang, Roger Gejman, Ali Mahta, Ying Zhong, Kimberley A. Rice, Yunli Zhou, Pornsuk Cheunsuchon, David N. Louis, Anne Klibanski
Concurrent <i>CIC</i> mutations, <i>IDH</i> mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers
Stephen Yip, Yaron S.N. Butterfield, Olena Morozova, Suganthi Chittaranjan, Michael Blough, Jianghong An, İnanç Birol, Charles Chesnelong, Readman Chiu, Eric Chuah, Richard Corbett, Roderick Docking, Marlo Firme, Martin Hirst, Shaun D. Jackman, Aly Karsan, Haiyan Li, David N. Louis, Alexandra Maslova, Richard A. Moore, Annie Moradian, Karen Mungall, Marco Perizzolo, Jenny Q. Qian, Glòria Roldán, Eric E. Smith, Jessica Tamura‐Wells, Nina Thiessen, Richard Varhol, Samuel Weiss, Wei Wu, Sean Young, Yongjun Zhao, Andrew J. Mungall, Steven J.M. Jones, Gregg B. Morin, Jennifer A. Chan, J. Gregory Cairncross, Marco A. Marra
Bead-based profiling of tyrosine kinase phosphorylation identifies SRC as a potential target for glioblastoma therapy
Jinyan Du, Paula Bernasconi, Karl R. Clauser, D.R. Mani, Stephen P. Finn, Rameen Beroukhim, Melissa Burns, Bina Julian, Xiao Peng, Haley Hieronymus, Rebecca L. Maglathlin, Timothy A. Lewis, Linda M. Liau, Phioanh L. Nghiemphu, Ingo K. Mellinghoff, David N. Louis, Massimo Loda, Steven A. Carr, Andrew L. Kung, Todd R. Golub