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Jonathan Stephens

ResearcherPublications, citations & collaboration network

Jonathan Stephens is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Jonathan Stephens have?

ScholarIQindexed works

Jonathan Stephens has 188 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Jonathan Stephens have?

ScholarIQcitation count

Jonathan Stephens has 25,019 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Jonathan Stephens?

ScholarIQh-index

Jonathan Stephens has an h-index of 67 in OpenAlex.

What is the i10-index of Jonathan Stephens?

ScholarIQi10-index

Jonathan Stephens has an i10-index of 125 in OpenAlex.

What is the ORCID of Jonathan Stephens?

ScholarIQorcid

The ORCID for Jonathan Stephens is on the source record.

What is the OpenAlex record for Jonathan Stephens?

ScholarIQopenalex

The OpenAlex for Jonathan Stephens is on the source record.

What are the most-cited papers on Jonathan Stephens?

ScholarIQmost cited works
SARS-CoV-2 evolution during treatment of chronic infection
Steven A. Kemp, Dami A. Collier, Rawlings Datir, Isabella A.T.M. Ferreira, Salma Gayed, Aminu S. Jahun, Myra Hosmillo, Chloe Rees-Spear, Petra Mlčochová, Ines Ushiro Lumb, David J. Roberts, Anita Chandra, Nigel Temperton, Principal investigators, Stephen Baker, Gordon Dougan, Christoph Hess, Nathalie Kingston, Paul J. Lehner, Paul Lyons, Nicholas J. Matheson, Willem H. Owehand, Caroline Saunders, Charlotte Summers, James Thaventhiran, Mark Toshner, Michael P. Weekes, Ashlea Bucke, Jo Calder, Laura Canna, Jason Domingo, Anne Elmer, Stewart Fuller, Julie Harris, Sarah Hewitt, Jane Kennet, Sherly Jose, Jenny Kourampa, Anne Meadows, Criona O’Brien, Jane Price, Cherry Publico, Rebecca Rastall, Carla M. S. Ribeiro, Jane Rowlands, Valentina Ruffolo, Hugo Tordesillas, Sample logistics, Ben Bullman, Benjamin J. Dunmore, Stuart Fawke, Stefan Ting Graf, Josh Hodgson, Christopher Huang, Kelvin Hunter, Emma Jones, Ekaterina Legchenko, Cecilia Matara, Jennifer Martin, Federica Mescia, Ciara O’Donnell, Linda Pointon, Nicole Pond, Joy Shih, Rachel Sutcliffe, Tobias Tilly, Carmen Treacy, Zhen Tong, Jennifer Wood, Marta Wylot, Sample processing & data acquisition, Laura Bergamaschi, Ariana Betancourt, Georgie Bower, Chiara Cossetti, Aloka De, Madeline Epping, Stuart Fawke, Nick Gleadall, Richard Grenfell, Andrew Hinch, Oisín Huhn, Sarah Jackson, Isobel Jarvis, D. J. Lewis, Joe Marsden, Francesca Nice, Georgina Okecha, Ommar Omarjee, Marianne Perera, Nathan Richoz, Veronika Romashova, Natalia Savinykh Yarkoni, Rahul Sharma, Luca Stefanucci, Jonathan Stephens, Mateusz Strezlecki, Lori Turner, Eckart M. D. D. De Bie, Katherine Bunclark
Nature. 20211,087 CitationsOPEN ACCESS
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nick Craddock, Liz Forty, Katherine Gordon‐Smith, Elaine Green, Detelina Grozeva, Ian Jones, George Kirov, Michael O‘Donovan, Michael J. Owen, Ellie Russell, M. E. Hurles, Samuel C. Robson, C. Barnes, Donald F. Conrad, Kathy Stirrups, Jan Aerts, T. Daniel Andrews, Hazel Arbury, Anthony Attwood, Jeffrey C. Barrett, Inês Barroso, Sanjeev S. Bhaskar, John H. Burton, Chris M. Clee, Alison J. Coffey, Andrew Dunham, Sarah Edkins, Tomas Fitzgerald, Emma Gray, Rhian Gwilliam, Naomi Hammond, Husam Hebaishi, Eleanor Howard, Sarah Hunt, Cordelia F. Langford, Kevin Lewis, Kirsten McLay, Michael L. Mimmack, Ifejinelo Onyiah, Kimmo Palin, Michael A. Quail, Richard Redon, Carol Scott, Elilan Somaskantharajah, Armand Valsesia, Eleftheria Zeggini, Nigel P. Carter, Aarno Palotie, Chris Tyler‐Smith, Michael R. Stratton, Panos Deloukas, Dominic Kwiatkowski, Willem H. Ouwehand, Niall J. Cardin, Eleni Giannoulatou, Christopher Holmes, Jonathan Marchini, Christopher Yau, Adam Auton, Simon Myers, Zhan Su, Gil McVean, Peter Donnelly, Richard D. Pearson, Damjan Vukcevic, Jake Byrnes, Mahim Jain, Cecilia M. Lindgren, Julian Maller, Andrew P. Morris, Inga Prokopenko, Nigel W. Rayner, Robertson NP, Adrian V. S. Hill, Mark I. McCarthy, Vincent Plagnol, Oliver S. Burren, Jason D. Cooper, Kate Downes, Matt Hardy, Joanna M. M. Howson, Meeta Maisuria-Armer, Nigel Ovington, Helen Schuilenburg, Debbie J. Smyth, Helen E. Stevens, Neil Walker, Chris Wallace, Matthew Woodburn, John A. Todd, Martin D. Tobin, Louise V. Wain, J. Thompson, Paul R. Burton, Tariq Ahmad, Jennifer D. Jolley, Jennifer G. Sambrook, Jonathan Stephens, Nicholas A. Watkins, Stephen G. Ball
Nature. 2010817 CitationsOPEN ACCESS
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
Nature. 2020586 CitationsOPEN ACCESS
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
Keren Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Mégy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka, Vincent Plagnol, Christopher J. Penkett, Kathleen Stirrups, Roberta Rizzo, Genevieve Wright, Dragana Josifova, Maria Bitner‐Glindzicz, Richard H. Scott, Emma Clement, Louise Allen, Ruth Armstrong, Angela F. Brady, Jenny Carmichael, Manali Chitre, Robert Henderson, Jane A. Hurst, Robert E. MacLaren, Elaine Murphy, Joan Paterson, Elisabeth Rosser, Dorothy Thompson, Emma Wakeling, Willem H. Ouwehand, Michel Michaelides, Anthony T. Moore, Andrew R. Webster, F. Lucy Raymond, Timothy J. Aitman, Hana Alachkar, Sonia Ali, Louise Allen, David Allsup, Gautum Ambegaonkar, Julie Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Sofie Ashford, William F. Astle, Antony Attwood, Steve Austin, Chiara Bacchelli, Tamam Bakchoul, Tadbir K. Bariana, Helen Baxendale, David Bennett, Claire Bethune, Shahnaz Bibi, Maria Bitner‐Glindzicz, Marta Bleda, Harm Boggard, Paula Bolton‐Maggs, Claire Booth, John R. Bradley, Angie Brady, Matthew A. Brown, Michael J. Browning, Christine Bryson, Siobhan O. Burns, Paul Calleja, Natalie Canham, Jenny Carmichael, Keren Carss, Mark J. Caulfield, Elizabeth Chalmers, Anita Chandra, Patrick F. Chinnery, Manali Chitre, Colin Church, Emma Clement, Emma Clement, Virginia Clowes, Gerry Coghlan, Peter Collins, Nichola Cooper, Amanda Creaser-Myers, Rosa DaCosta, Louise C. Daugherty, Sophie Davies, John S. Davis, Minka De Vries, Patrick Deegan, Sri V. V. Deevi, Charu Deshpande, Lisa Devlin, Eleanor Dewhurst, Rainer Döffinger, Natalie Dormand, Elizabeth Drewe
The American Journal of Human Genetics. 2016490 CitationsOPEN ACCESS
Whole-genome sequencing of a sporadic primary immunodeficiency cohort
James Thaventhiran, Hana Lango Allen, Oliver S. Burren, William Rae, Daniel Greene, Emily Staples, Zinan Zhang, James H. R. Farmery, Ilenia Simeoni, Elizabeth Rivers, Jesmeen Maimaris, Christopher J. Penkett, Jonathan Stephens, Sri V. V. Deevi, Alba Sanchis‐Juan, Nicholas Gleadall, Moira Thomas, Ravishankar Sargur, Pavels Gordins, Helen E. Baxendale, Matthew A. Brown, Paul Tuijnenburg, Austen Worth, Steven Hanson, Rachel Linger, Matthew Buckland, Paula Rayner-Matthews, Kimberly Gilmour, Crina Samarghitean, Suranjith L. Seneviratne, David M. Sansom, Andy G. Lynch, Karyn Mégy, Eva Ellinghaus, David Ellinghaus, Silje F. Jørgensen, Tom H. Karlsen, Kathleen Stirrups, Antony J. Cutler, Dinakantha Kumararatne, Anita Chandra, David Edgar, Archana Herwadkar, Nichola Cooper, Sofia Grigoriadou, Aarnoud Huissoon, Sarah Goddard, Stephen Jolles, Catharina Schuetz, Felix Boschann, Stephen Abbs, Zoe Adhya, Julian Adlard, Maryam Afzal, Irshad Ahmed, Munaza Ahmed, Saeed Ahmed, Timothy J. Aitman, Hana Alachkar, Jayanthi Alamelu, Raza Alikhan, Carl E. Allen, Louise Allen, David Allsup, Arif Alvi, Gautam Ambegaonkar, Ariharan Anantharachagan, Philip Ancliff, Julie A. Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Rita Arya, Sofie Ashford, William J. Astle, Anthony Attwood, Steve Austin, Yeşim Aydınok, Waqar Ayub, Christian Babbs, Chiara Bacchelli, Trevor Baglin, Tamam Bakchoul, Tadbir K. Bariana, Jonathan Barratt, Julian Barwell, John Baski, Rachel W. Bates, Joana Batista, Helen E. Baxendale, Gareth Baynam, David Bennett, Claire Bethune, Neha Bhatnagar, Shahnaz Bibi, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Marta Bleda
Nature. 2020243 CitationsOPEN ACCESS

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