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Mary Porteous

ResearcherPublications, citations & collaboration network

Mary Porteous is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Mary Porteous have?

ScholarIQindexed works

Mary Porteous has 220 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Mary Porteous have?

ScholarIQcitation count

Mary Porteous has 21,298 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Mary Porteous?

ScholarIQh-index

Mary Porteous has an h-index of 62 in OpenAlex.

What is the i10-index of Mary Porteous?

ScholarIQi10-index

Mary Porteous has an i10-index of 141 in OpenAlex.

What is the OpenAlex record for Mary Porteous?

ScholarIQopenalex

The OpenAlex for Mary Porteous is on the source record.

What are the most-cited papers on Mary Porteous?

ScholarIQmost cited works
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
Kimberly A. McAllister, K.M. Grogg, David W. Johnson, Carol J. Gallione, Melanie A. Baldwin, Charles E. Jackson, E.A. Helmbold, Dorene S. Markel, Wendy McKinnon, J. Murrel, Mary Kay McCormick, M. A. Pericak‐Vance, Peter Heutink, Ben A. Oostra, T. Haitjema, C.J.J. Westerman, Mary Porteous, Alan E. Guttmacher, Michelle Letarte, Douglas A. Marchuk
Nature Genetics. 19941,503 CitationsOPEN ACCESS
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
David W. Johnson, Jonathan Berg, Melanie A. Baldwin, Carol J. Gallione, Ivonne Marondel, Sang-Heon Yoon, Timothy T. Stenzel, Marcy C. Speer, M. A. Pericak‐Vance, Austin G. Diamond, Alan E. Guttmacher, Charles E. Jackson, Liliana Attisano, Raju Kucherlapati, Mary Porteous, Douglas A. Marchuk
Nature Genetics. 19961,130 Citations
International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia
Marie E. Faughnan, Valerie A. Palda, Guadalupe García–Tsao, Urban W. Geisthoff, Jamie McDonald, Deborah D. Proctor, John C. Spears, Dale Brown, Elisabetta Buscarini, Mark S. Chesnutt, Vincent Cottin, Arupa Ganguly, James R. Gossage, Alan E. Guttmacher, Robert H. Hyland, Shelley Kennedy, Joshua R. Korzenik, Johannes J. Mager, Augustin Ozanne, Jay F. Piccirillo, Daniel Picus, Henri Plauchu, Mary Porteous, Reed E. Pyeritz, Douglas A. Ross, Carlo Sabbà, Karen L. Swanson, P. B. Terry, M. Christopher Wallace, C. J. J. Westermann, Robert I. White, Lawrence H. Young, Roberto Zarrabeitia
Journal of Medical Genetics. 20091,081 Citations
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, Zhancheng Zhang, Kevin J. Arvai, Ruth Y. Eberhardt, Giuseppe Gallone, Stefan H. Lelieveld, Hilary C. Martin, Jeremy F. McRae, Patrick Short, Rebecca I. Torene, Elke de Boer, Petr Danecek, Eugene J. Gardner, Ni Huang, Jenny Lord, Iñigo Martincorena, Rolph Pfundt, Margot R.F. Reijnders, Alison Yeung, Helger G. Yntema, Deciphering Developmental Disorders Study, Sílvia Borràs, Caroline Clark, John Dean, Zosia Miedzybrodzka, Alison Ross, Stephen Tennant, Tabib Dabir, Deirdre Donnelly, Mervyn Humphreys, Alex Magee, Vivienne McConnell, Shane McKee, Susan McNerlan, Patrick J. Morrison, Gillian Rea, Fiona Stewart, Trevor Cole, Nicola Cooper, Lisa Cooper‐Charles, Helen Cox, Lily Islam, Joanna Jarvis, Rebecca Keelagher, Derek Lim, Dominic McMullan, Jenny Morton, Swati Naik, Mary O’Driscoll, Kai‐Ren Ong, Deborah Osio, Nicola Ragge, Sarah Turton, Julie Vogt, Denise Williams, Simon Bodek, Alan Donaldson, Alison Hills, Karen Low, Ruth Newbury‐Ecob, Andrew Norman, Eileen Roberts, Ingrid Scurr, Sarah Smithson, Madeleine Tooley, Steve Abbs, Ruth Armstrong, Carolyn Dunn, Simon Holden, Soo‐Mi Park, Joan Paterson, Lucy Raymond, Evan Reid, Richard Sandford, Ingrid Simonic, Marc Tischkowitz, Geoff Woods, Lisa Bradley, Joanne Comerford, Andrew Green, Sally Ann Lynch, Shirley McQuaid, Brendan Mullaney, Jonathan Berg, David Goudie, Eleni Mavrak, Joanne McLean, Catherine McWilliam, Eleanor Reavey, Tara Azam, Elaine Cleary, Andrew P. Jackson, Wayne Lam, Anne Lampe, David Moore, Mary Porteous, Emma L. Baple, Júlia Baptista
Nature. 2020690 CitationsOPEN ACCESS
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Albert Tenesa, Susan M. Farrington, James Prendergast, Mary Porteous, Marion Walker, Naila Haq, Rebecca A. Barnetson, Evropi Τheodoratou, Roseanne Cetnarskyj, Nicola Cartwright, Colin A. Semple, Andrew J. Clark, Fiona Jane Reid, Lorna Smith, Kostas Kavoussanakis, Thibaud Koessler, Paul D.P. Pharoah, Stephan Buch, Clemens Schafmayer, Jürgen Tepel, Stefan Schreiber, Henry Völzke, Carsten Oliver Schmidt, Jochen Hampe, Jenny Chang‐Claude, Michael Hoffmeister, Hermann Brenner, Stefan Wilkening, Federico Canzian, Gabriel Capellá, Vı́ctor Moreno, Ian J. Deary, John M. Starr, Ian Tomlinson, Zoe Kemp, Kimberley Howarth, Luis G. Carvajal‐Carmona, Emily L. Webb, Peter Broderick, Jayaram Vijayakrishnan, Richard S. Houlston, Gad Rennert, Dennis G. Ballinger, Laura S. Rozek, Stephen B. Gruber, Koichi Matsuda, Tomohide Kidokoro, Yusuke Nakamura, Brent W. Zanke, Celia M.T. Greenwood, Jagadish Rangrej, Rafal Kustra, Alexandre Montpetit, Thomas J. Hudson, Steven Gallinger, Harry Campbell, Malcolm G. Dunlop
Nature Genetics. 2008605 CitationsOPEN ACCESS

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