ScholarIQanswers from OpenAlex & ORCID
Catherine Williamson
ResearcherPublications, citations & collaboration network
Catherine Williamson is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Catherine Williamson have?
ScholarIQindexed works
Catherine Williamson has 434 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Catherine Williamson have?
ScholarIQcitation count
Catherine Williamson has 20,548 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Catherine Williamson?
ScholarIQh-index
Catherine Williamson has an h-index of 73 in OpenAlex.
What is the i10-index of Catherine Williamson?
ScholarIQi10-index
Catherine Williamson has an i10-index of 197 in OpenAlex.
What is the ORCID of Catherine Williamson?
ScholarIQorcid
The ORCID for Catherine Williamson is on the source record.
What is the OpenAlex record for Catherine Williamson?
ScholarIQopenalex
The OpenAlex for Catherine Williamson is on the source record.
What are the most-cited papers on Catherine Williamson?
ScholarIQmost cited works
Saving Mothers’ Lives: Reviewing maternal deaths to make motherhood safer: 2006–2008
Roch Cantwell, T. H. Clutton-Brock, Griselda Cooper, Andrew Dawson, James Drife, Debbie Garrod, Ann Harper, Diana Hulbert, Sebastian Lucas, J. H. McClure, Harry Millward-Sadler, James P Neilson, Catherine Nelson‐Piercy, Jane E. Norman, Colm O’Herlihy, Margaret R. Oates, Judy Shakespeare, Michael de Swiet, Catherine Williamson, Valerie Beale, Marian Knight, Christopher E. Lennox, Alison Miller, Dharmishta Parmar, Jane Rogers, Anna Springett
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J. Astle, Karyn Mégy, Stefan Gräf, Daniel Greene, Olga Shamardina, Hana Lango Allen, Alba Sanchis‐Juan, Mattia Frontini, Chantal Thys, Jonathan Stephens, Rutendo Mapeta, Oliver S. Burren, Kate Downes, Matthias Haimel, Salih Tuna, Sri V. V. Deevi, Timothy J. Aitman, David Bennett, Paul Calleja, Keren Carss, Mark J. Caulfield, Patrick F. Chinnery, Peter Dixon, Daniel P. Gale, Roger James, Ania Koziell, Michael A. Laffan, Adam P. Levine, Eamonn R. Maher, Hugh S. Markus, Joannella Morales, Nicholas W. Morrell, Andrew Mumford, Elizabeth Ormondroyd, Stuart Rankin, Augusto Rendon, Sylvia Richardson, Irene Roberts, Noémi Roy, Moin A. Saleem, Kenneth G. C. Smith, Hannah Stark, Rhea Tan, Andreas C. Themistocleous, Adrian J. Thrasher, Hugh Watkins, Andrew R. Webster, Martin R. Wilkins, Catherine Williamson, James Whitworth, Sean Humphray, David R. Bentley, NIHR BioResource for the 100,000 Genomes Project, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, David R. Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme C. Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John R. Bradley, Eugene Bragin, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
Valgerður Steinthórsdóttir, Ralph McGinnis, Nicholas Williams, Lilja Stefánsdóttir, Guðmar Þorleifsson, Scott Shooter, João Fadista, Jon K. Sigurdsson, Kirsi Auro, Galina Berezina, Maria Carolina Borges, Suzannah Bumpstead, Jonas Bybjerg‐Grauholm, Irina Colgiu, Vivien A. Dolby, Frank Dudbridge, Stephanie M. Engel, Christopher Franklin, Michael L. Frigge, Yr Frisbæk, Reynir Tómas Geirsson, Frank Geller, Sólveig Grétarsdóttir, Daníel F. Guðbjartsson, Quaker E. Harmon, David M. Hougaard, Tatyana Hegay, Anna Helgadóttir, Sigrun Hjartardottir, Tiina Jääskeläinen, Hrefna Johannsdottir, Ingileif Jónsdóttir, Thorhildur Juliusdottir, Noor Kalsheker, A. K. Kasimov, John P. Kemp, Katja Kivinen, Kari Klungsøyr, Wai Lee, Mads Melbye, Zosia Miedzybrodska, Ashley Moffett, Dilbar Najmutdinova, Firuza Nishanova, Thorunn A. Olafsdottir, Markus Perola, Fiona Broughton Pipkin, Lucilla Poston, Gordon Prescott, Saedís Saevarsdóttir, Damilya Salimbayeva, Paula J. Scaife, Line Skotte, Eleonora Staines-Urias, Ólafur Andri Stefánsson, Karina Meden Sørensen, Liv Cecilie Vestrheim Thomsen, Vinicius Tragante, Lill Trogstad, Nigel Simpson, Hannele Laivuori, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Linda Morgan, Fiona Broughton Pipkin, Noor Kalsheker, James J. Walker, Sheila Macphail, Mark D. Kilby, Marwan Habiba, Catherine Williamson, Kevin M. O’Shaughnessy, Shaughn O’Brien, Alan C. Cameron, Christopher W.G. Redman, Martin Farrall, Mark J. Caulfield, Anna F. Dominiczak, Tamara Aripova, Juan P. Casas, Anna F. Dominiczak, James J. Walker, Unnur Þorsteinsdóttir, Ann‐Charlotte Iversen, Bjarke Feenstra, Debbie A. Lawlor, Heather A. Boyd, Per Magnus, Hannele Laivuori, Nodira Zakhidova, Gulnara Svyatova, Kāri Stefánsson, Linda Morgan
Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension
Charaka Hadinnapola, Marta Bleda, Matthias Haimel, Nicholas Screaton, Andrew J. Swift, Peter Dorfmüller, Stephen Preston, Mark Southwood, Jules Hernández‐Sánchez, Jennifer M. Martin, Carmen Treacy, Katherine Yates, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Simon Gibbs, Barbara Girerd, Simon Holden, Marc Humbert, David G. Kiely, Allan Lawrie, Rajiv D. Machado, R Mackenzie Ross, Shahin Moledina, David Montani, Michael Newnham, Andrew J. Peacock, Joanna Pepke‐Żaba, Paula Rayner-Matthews, Olga Shamardina, Florent Soubrier, Laura Southgate, Jay Suntharalingam, Mark Toshner, Richard C. Trembath, Anton Vonk Noordegraaf, Martin R. Wilkins, Stephen J. Wort, John Wharton, Stefan Gräf, Nicholas W. Morrell, Timothy J. Aitman, David Bennett, Mark J. Caulfield, Patrick F. Chinnery, Daniel P. Gale, Ania Koziell, Taco W. Kuijpers, Michael Laffan, Eamonn R. Maher, Hugh S. Markus, Willem H. Ouwehand, David J. Perry, F. Lucy Raymond, Irene Roberts, Kenneth G. C. Smith, Adrian J. Thrasher, Hugh Watkins, Catherine Williamson, Geoffrey Woods, Sofie Ashford, John R. Bradley, Debra Fletcher, Tracey Hammerton, Roger James, Nathalie Kingston, Willem H. Ouwehand, Christopher J. Penkett, F. Lucy Raymond, Kathleen Stirrups, Marijke Veltman, Tim Young, Sofie Ashford, Matthew A. Brown, Emma Clement, John Davis, Eleanor Dewhurst, Marie Erwood, Amy Frary, Rachel Linger, Sofia Papadia, Karola Rehnström, Hannah Stark, David Allsup, Steve Austin, Tamam Bakchoul, Tadbir K. Bariana, Paula Bolton‐Maggs, Elizabeth Chalmers, Peter Collins, Wendy N. Erber, Tamara Everington, Rémi Favier, Kathleen Freson, Bruce Furie, Michael Gattens, Keith Gomez, Daniel Greene