ScholarIQanswers from OpenAlex & ORCID
Cathryn M. Lewis
ResearcherPublications, citations & collaboration network
Cathryn M. Lewis is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Cathryn M. Lewis have?
ScholarIQindexed works
Cathryn M. Lewis has 935 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Cathryn M. Lewis have?
ScholarIQcitation count
Cathryn M. Lewis has 90,250 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Cathryn M. Lewis?
ScholarIQh-index
Cathryn M. Lewis has an h-index of 122 in OpenAlex.
What is the i10-index of Cathryn M. Lewis?
ScholarIQi10-index
Cathryn M. Lewis has an i10-index of 446 in OpenAlex.
What is the ORCID of Cathryn M. Lewis?
ScholarIQorcid
The ORCID for Cathryn M. Lewis is on the source record.
What is the OpenAlex record for Cathryn M. Lewis?
ScholarIQopenalex
The OpenAlex for Cathryn M. Lewis is on the source record.
What are the most-cited papers on Cathryn M. Lewis?
ScholarIQmost cited works
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S Hong Lee, Bryan Mowry, E Byrne, Peter M. Visscher, Naomi R. Wray, Stephan Ripke, B M Neale, Shaun Purcell, Verneri Anttila, Soumya Raychaudhuri, Mark J. Daly, Roy H. Perlis, Sarah E. Bergen, Kimberly Chambert, Steven A. McCarroll, Jennifer L. Moran, Colm Ó'Dúshláine, Lizzy Rossin, Edward Scolnick, Jordan W. Smoller, Stephen V Faraone, Douglas M. Ruderfer, Pamela Sklar, P H Lee, Anita Thapar, Christine Fraser, Lyudmila Georgieva, Katherine Gordon‐Smith, Detelina Grozeva, Marian L. Hamshere, Peter A Holmans, I. Jones, George Kirov, Valentina Moskvina, Ivan Nikolov, Michael J Owen, Nigel Williams, Stanley Zammit, Michael O‘Donovan, Nicholas Craddock, Michael E. Goddard, John S. Witte, Devin Absher, Richard M. Myers, Ingrid Agartz, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Huda Akil, Fan Meng, Robert C. Thompson, Stanley J Watson, Farooq Amin, Adebayo Anjorin, Nicholas Bass, Khalid Choudhury, Hugh Gurling, Radhika Kandaswamy, Robert Krasucki, Jacob Lawrence, Andrew McQuillin, Jonathan Pimm, Vinay Puri, Richard Anney, Paul Cormican, Aiden Corvin, Gary Donohoe, Louise Gallagher, Michael Gill, Elaine Kenny, Derek W. Morris, Emma M. Quinn, Dan E. Arking, Aravinda Chakravarti, Philip Asherson, Gerome Breen, David Collier, Ian Craig, Anne Farmer, Jonna Kuntsi, Cathryn M. Lewis, Peter McGuffin, Maria Helena Pinto de Azevedo, Guiomar Oliveira, Lena Backlund, Louise Frisén, Urban Ösby, Martin Schalling, Judith A. Badner, Elliot S. Gershon, Anthony Bailey, Tobias Banaschewski, Jack D. Barchas, Michael R. Barnes, Thomas B. Barrett, Agatino Battaglia, Michael Bauer, Mónica Bayés, Frank Bellivier
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Rainer Malik, Ganesh Chauhan, Matthew Traylor, Muralidharan Sargurupremraj, Yukinori Okada, Aniket Mishra, Loes C.A. Rutten‐Jacobs, Anne-Katrin Giese, Sander W. van der Laan, Sólveig Grétarsdóttir, Christopher D. Anderson, Michael Chong, Hieab H.H. Adams, Tetsuro Ago, Peter Almgren, Philippe Amouyel, Hakan Ay, Traci M. Bartz, Oscar R. Benavente, Steve Bevan, Giorgio B. Boncoraglio, Robert D. Brown, Adam S. Butterworth, Caty Carrera, Cara L. Carty, Daniel I. Chasman, Wei‐Min Chen, John W. Cole, Adolfo Correa, Ioana Cotlarciuc, Carlos Cruchaga, John Danesh, Paul I. W. de Bakker, Anita L. DeStefano, Marcel den Hoed, Qing Duan, Stefan T. Engelter, Guido J. Falcone, Rebecca F. Gottesman, Raji P. Grewal, Vilmundur Guðnason, Stefan Gustafsson, Jeffrey Haessler, Tamara B. Harris, Ahamad Hassan, Aki S. Havulinna, Susan R. Heckbert, Elizabeth G. Holliday, George Howard, Fang‐Chi Hsu, Hyacinth I. Hyacinth, M. Arfan Ikram, Erik Ingelsson, Marguerite R. Irvin, Xueqiu Jian, Jordi Jiménez‐Conde, Julie A. Johnson, J. Wouter Jukema, Masahiro Kanai, Keith L. Keene, Brett Kissela, Dawn Kleindorfer, Charles Kooperberg, Michiaki Kubo, Leslie A. Lange, Carl D. Langefeld, Claudia Langenberg, Lenore J. Launer, Jin‐Moo Lee, Robin Lemmens, Didier Leys, Cathryn M. Lewis, Wei‐Yu Lin, Arne G. Lindgren, Erik Lorentzen, Patrik K. E. Magnusson, Jane Maguire, Ani Manichaikul, Patrick F. McArdle, James F. Meschia, Braxton D. Mitchell, Thomas H. Mosley, Michael A. Nalls, Toshiharu Ninomiya, Martin O’Donnell, Bruce M. Psaty, Sara L. Pulit, Kristiina Rannikmäe, Alex P. Reiner, Kathryn M. Rexrode, Kenneth Rice, Stephen S. Rich, Paul M. Ridker, Natalia S. Rost, Peter M. Rothwell, Jerome I. Rotter, Tatjana Rundek, Ralph L. Sacco, Saori Sakaue, Michèle M. Sale
A mega-analysis of genome-wide association studies for major depressive disorder
Stephan Ripke, Naomi R. Wray, Cathryn M. Lewis, Steven P. Hamilton, Myrna M. Weissman, Gerome Breen, Enda M. Byrne, Douglas Blackwood, Dorret I. Boomsma, Sven Cichon, Andrew C. Heath, Florian Holsboer, Susanne Lucae, Pamela A. F. Madden, Nicholas G. Martin, Peter McGuffin, Pierandrea Muglia, Markus M. Nöethen, Brenda P Penninx, Michele L. Pergadia, James B. Potash, Marcella Rietschel, D. Y. Lin, Bertram Müller‐Myhsok, Jianxin Shi, Stacy Steinberg, Hans J. Grabe, Paul Lichtenstein, Patrik K. E. Magnusson, Roy H. Perlis, Martin Preisig, Jordan W. Smoller, Kāri Stefánsson, Rudolf Uher, Zoltán Kutalik, Katherine E. Tansey, Alexander Teumer, Alexander Viktorin, Michael R. Barnes, Thomas Bettecken, Elisabeth B. Binder, René Breuer, Víctor M. Castro, Susanne Churchill, William Coryell, Nick Craddock, Ian Craig, Darina Czamara, Eco J. C. de Geus, Franziska Degenhardt, Anne Farmer, Maurizio Fava, Josef Frank, Vivian S. Gainer, Patience Gallagher, Scott D. Gordon, Sergey Goryachev, Magdalena Groß, Michel Guipponi, Anjali K. Henders, Stefan Herms, Ian B. Hickie, Susanne Hoefels, Witte J.G. Hoogendijk, Jouke‐Jan Hottenga, Dan V. Iosifescu, Marcus Ising, Ian D. Jones, Lisa Jones, Tzeng Jung-Ying, James A. Knowles, Isaac S. Kohane, Martin Kohli, Ania Korszun, Mikael Landén, William Lawson, Glyn Lewis, Donald J. MacIntyre, Wolfgang Maier, Manuel Mattheisen, Patrick J. McGrath, Andrew M. McIntosh, Alan McLean, Christel M. Middeldorp, Lefkos Middleton, Grant M Montgomery, Shawn N. Murphy, Matthias Nauck, Willem A. Nolen, Dale R. Nyholt, Michael O‘Donovan, Högni Óskarsson, Nancy L. Pedersen, William A. Scheftner, Andrea Schulz, Thomas G. Schulze, Stanley I. Shyn, Engilbert Sigurðsson, Susan L. Slager, Johannes H. Smit
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
Miles Parkes, Jeffrey C. Barrett, Natalie J. Prescott, Mark Tremelling, Carl A. Anderson, Sheila Fisher, Roland G. Roberts, Elaine R. Nimmo, Fraser Cummings, Dianne Soars, Hazel E. Drummond, Charlie W. Lees, Saud Khawaja, Richard D. Bagnall, Denis Burke, Catherine E Todhunter, Tariq Ahmad, Clive M. Onnie, Wendy L. McArdle, David P. Strachan, Graeme Bethel, Claire Bryan, Cathryn M. Lewis, Panos Deloukas, Alastair Forbes, Jeremy Sanderson, Derek P. Jewell, Jack Satsangi, John Mansfield, Lon R. Cardon, Christopher G. Mathew
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
Jochen Hampe, Andrew Cuthbert, Peter J.P. Croucher, Muddassar M. Mirza, Silvia Mascheretti, Sheila Fisher, H Frenzel, Kathy King, Anja Hasselmeyer, Andrew JS MacPherson, Stephen Bridger, Sander van Deventer, Alastair Forbes, Susanna Nikolaus, John Edward Lennard-Jones, Ulrich R. Foelsch, Michael Krawczak, Cathryn M. Lewis, Stefan Schreiber, Christopher G. Mathew