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Mark Lathrop

ResearcherPublications, citations & collaboration network

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

How many works does Mark Lathrop have?

ScholarIQindexed works

Mark Lathrop has 145 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 Lathrop have?

ScholarIQcitation count

Mark Lathrop has 29,593 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Mark Lathrop?

ScholarIQh-index

Mark Lathrop has an h-index of 66 in OpenAlex.

What is the i10-index of Mark Lathrop?

ScholarIQi10-index

Mark Lathrop has an i10-index of 109 in OpenAlex.

What is the OpenAlex record for Mark Lathrop?

ScholarIQopenalex

The OpenAlex for Mark Lathrop is on the source record.

What are the most-cited papers on Mark Lathrop?

ScholarIQmost cited works
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Jeffrey C. Barrett, Sarah Hansoul, Dan L. Nicolae, Judy H. Cho, Richard H. Duerr, John D. Rioux, Steven R. Brant, Mark S. Silverberg, Kent D. Taylor, M. Michael Barmada, Alain Bitton, Themistocles Dassopoulos, Lisa W. Datta, Todd J. Green, Anne M. Griffiths, Emily O. Kistner, Michael T. Murtha, Miguel Regueiro, Jerome I. Rotter, L. Philip Schumm, A. Hillary Steinhart, Stephan R. Targan, Ramnik J. Xavier, Cécile Libioulle, Cynthia Sandor, Mark Lathrop, Jacques Bélaïche, Olivier Dewit, Marta Gut, Simon Heath, Debby Laukens, Myriam Mni, Paul Rutgeerts, A. Van Gossum, Diana Zélénika, Denis Franchimont, Jean‐Pierre Hugot, Martine De Vos, Séverine Vermeire, Édouard Louis, Lon R. Cardon, Carl A. Anderson, Hazel E. Drummond, Elaine R. Nimmo, Tariq Ahmad, Natalie J. Prescott, Clive M. Onnie, Sheila Fisher, Jonathan Marchini, Jilur Ghori, Suzannah Bumpstead, Rhian Gwilliam, Mark Tremelling, Panos Deloukas, John Mansfield, Derek P. Jewell, Jack Satsangi, Christopher G. Mathew, Miles Parkes, Michel Georges, Mark J. Daly
Nature Genetics. 20082,640 CitationsOPEN ACCESS
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
Claire S. Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kévin Mouzat, Dalila Pinto, Jennifer Howe, Nathalie Lemière, Christelle M. Durand, Jessica Guibert, Elodie Ey, Roberto Toro, Hugo Peyre, Alexandre Mathieu, Frédérique Amsellem, Maria Råstam, I. Carina Gillberg, Gudrun Rappold, Richard Holt, Anthony P. Monaco, Elena Maestrini, Pilar Galán, Delphine Héron, Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron
PLoS Genetics. 2014672 CitationsOPEN ACCESS
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma
Maria Teresa Landi, Nilanjan Chatterjee, Kai Yu, Lynn R. Goldin, Alisa M. Goldstein, Melissa Rotunno, Lisa Mirabello, Kevin B. Jacobs, William Wheeler, Meredith Yeager, Andrew W. Bergen, Qizhai Li, Dario Consonni, Angela Cecilia Pesatori, Sholom Wacholder, Michael J. Thun, W. Ryan Diver, Martin M. Oken, Jarmo Virtamo, Demetrius Albanes, Zhaoming Wang, Laurie Burdette, Kimberly F. Doheny, Elizabeth Pugh, Cathy C. Laurie, Paul Brennan, Rayjean Hung, Valérie Gaborieau, James McKay, Mark Lathrop, John McLaughlin, Ying Wang, Ming‐Sound Tsao, Margaret R. Spitz, Yufei Wang, Hans E. Krokan, Lars J. Vatten, Frank Skorpen, Egil Arnesen, Simone Benhamou, Christine Bouchard, Andres Metsapalu, Tõnu Vooder, Mari Nelis, Kristian Välk, John K. Field, Chu Chen, Gary E. Goodman, Patrick Sulem, Guðmar Þorleifsson, Þórunn Rafnar, Timothy Eisen, Wiebke Sauter, Albert Rosenberger, Heike Bickeböller, Angela Risch, Jenny Chang‐Claude, H.‐Erich Wichmann, Kari Stefansson, Richard S. Houlston, Christopher I. Amos, Joseph F. Fraumeni, Sharon A. Savage, Pier Alberto Bertazzi, Margaret A. Tucker, Stephen Chanock, Neil E. Caporaso
The American Journal of Human Genetics. 2009509 CitationsOPEN ACCESS
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma
Maria Teresa Landi, Nilanjan Chatterjee, Kai Yu, Lynn R. Goldin, Alisa M. Goldstein, Melissa Rotunno, Lisa Mirabello, Kevin B. Jacobs, William Wheeler, Meredith Yeager, Andrew W. Bergen, Qizhai Li, Dario Consonni, Angela Cecilia Pesatori, Sholom Wacholder, Michael J. Thun, W. Ryan Diver, Martin M. Oken, Jarmo Virtamo, Demetrius Albanes, Zhaoming Wang, Laurie Burdette, Kimberly F. Doheny, Elizabeth Pugh, Cathy C. Laurie, Paul Brennan, Rayjean Hung, Valérie Gaborieau, James McKay, Mark Lathrop, John McLaughlin, Ying Wang, Ming‐Sound Tsao, Margaret R. Spitz, Yufei Wang, Hans E. Krokan, Lars J. Vatten, Frank Skorpen, Egil Arnesen, Simone Benhamou, Christine Bouchard, Andres Metspalu, Tõnu Vooder, Mari Nelis, Kristian Välk, John K. Field, Chu Chen, Gary Goodman, Patrick Sulem, Guðmar Þorleifsson, Þórunn Rafnar, Timothy Eisen, Wiebke Sauter, Albert Rosenberger, Heike Bickeböller, Angela Risch, Jenny Chang-Claude, H. Erich Wichmann, Kari Stefansson, Richard S. Houlston, Christopher I. Amos, Joseph F. Fraumeni, Sharon A. Savage, Pier Alberto Bertazzi, Margaret A. Tucker, Stephen Chanock, Neil E. Caporaso
The American Journal of Human Genetics. 2011506 CitationsOPEN ACCESS
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Claire S. Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Råstam, Henrik Anckarsäter, Gudrun Nygren, I. Carina Gillberg, Jonas Melke, Roberto Toro, Béatrice Regnault, Fabien Fauchereau, Oriane Mercati, Nathalie Lemière, David Skuse, Martin Poot, Richard Holt, Anthony P. Monaco, Irma Järvelä, Katri Kantojärvi, Raija Vanhala, Sarah Curran, David Collier, Patrick Bolton, Andreas G. Chiocchetti, Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana Filipa Sequeira, Bárbara Oliveira, Astrid M. Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zélénika, Marc Délepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie–Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron
PLoS Genetics. 2012446 CitationsOPEN ACCESS

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