ScholarIQanswers from OpenAlex & ORCID
Trevor Cole
ResearcherPublications, citations & collaboration network
Trevor Cole is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Trevor Cole have?
ScholarIQindexed works
Trevor Cole has 191 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Trevor Cole have?
ScholarIQcitation count
Trevor Cole has 17,269 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Trevor Cole?
ScholarIQh-index
Trevor Cole has an h-index of 67 in OpenAlex.
What is the i10-index of Trevor Cole?
ScholarIQi10-index
Trevor Cole has an i10-index of 119 in OpenAlex.
What is the OpenAlex record for Trevor Cole?
ScholarIQopenalex
The OpenAlex for Trevor Cole is on the source record.
What are the most-cited papers on Trevor Cole?
ScholarIQmost cited works
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
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Lynn M. Boyden, Murim Choi, Keith A. Choate, Carol Nelson‐Williams, Anita Farhi, Hakan R. Toka, Irina R. Tikhonova, Robert Bjornson, Shrikant Mane, Giacomo Colussi, Marcel Lebel, Richard D. Gordon, Ben A. Semmekrot, A. Poujol, Matti Välimäki, Maria Elisabetta De Ferrari, Sami A. Sanjad, Michael Gutkin, Fiona E. Karet, Joseph Tucci, Jim Stockigt, Kim M. Keppler‐Noreuil, Craig Porter, Sudhir Anand, Margo L. Whiteford, Ira D. Davis, Stephanie Dewar, Alberto Bettinelli, Jeffrey J. Fadrowski, Craig W. Belsha, Tracy E. Hunley, Raoul D. Nelson, Howard Trachtman, Trevor Cole, Maury Pinsk, Detlef Böckenhauer, Mohan Shenoy, Priya Vaidyanathan, John W. Foreman, Majid Rasoulpour, Farook Thameem, Hania Z. Al-Shahrouri, Jai Radhakrishnan, Ali G. Gharavi, Béatrice Goilav, Richard P. Lifton
Association of Type and Location of<i>BRCA1</i>and<i>BRCA2</i>Mutations With Risk of Breast and Ovarian Cancer
Timothy R. Rebbeck, Nandita Mitra, Fei Wan, Olga M. Sinilnikova, Sue Healey, Lesley McGuffog, Sylvie Mazoyer, Georgia Chenevix‐Trench, Douglas F. Easton, Antonis C. Antoniou, Katherine L. Nathanson, Yael Laitman, Anya Kushnir, Shani Paluch–Shimon, Raanan Berger, Jamal Zidan, Eitan Friedman, Hans Ehrencrona, Marie Stenmark‐Askmalm, Zakaria Einbeigi, Niklas Loman, Katja Harbst, Johanna Rantala, Beatrice Melin, Dezheng Huo, Olufunmilayo I. Olopade, Joyce Seldon, Patricia A. Ganz, Robert L. Nussbaum, Salina Chan, Kunle Odunsi, Simon A. Gayther, Susan M. Domchek, Banu Arun, Karen H. Lu, Gillian Mitchell, Beth Y. Karlan, Christine Walsh, Jenny Lester, Andrew K. Godwin, Harsh B. Pathak, Eric A. Ross, Mary B. Daly, Alice S. Whittemore, Esther M. John, Alexander Miron, Mary Beth Terry, Wendy K. Chung, David E. Goldgar, Saundra S. Buys, Ramūnas Janavičius, Laima Tihomirova, Nadine Tung, Cecilia M. Dorfling, Elizabeth J. van Rensburg, Linda Steele, Susan L. Neuhausen, Yuan Chun Ding, Bent Ejlertsen, Anne‐Marie Gerdes, Thomas van Overeem Hansen, Teresa Ramón y Cajal, Ana Osório, Javier Benı́tez, Javier Godino, María‐Isabel Tejada, M. Durán, Jeffrey N. Weitzel, Kristie Bobolis, Sharon Sand, Annette Campbell Fontaine, Antonella Savarese, Barbara Pasini, Bernard Peissel, Bernardo Bonanni, Daniela Zaffaroni, Francesca Vignolo-Lutati, Giulietta Scuvera, Giuseppe Giannini, Loris Bernard, Maurizio Genuardi, Paolo Radice, Riccardo Dolcetti, Siranoush Manoukian, Valeria Pensotti, Viviana Gismondi, Drakoulis Yannoukakos, Florentia Fostira, Judy E. Garber, Diana Torres, Muhammad Usman Rashid, Ute Hamann, Susan Peock, Debra Frost, Radka Platte, D. Gareth Evans, Rosalind A. Eeles, Rosemarie Davidson, Diana Eccles, Trevor Cole
Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in<i>AIP</i>Mutation Carriers
Laura C. Hernández‐Ramírez, Plamena Gabrovska, Judit Dénes, Karen Stals, Giampaolo Trivellin, Daniel Tilley, Francesco Ferraù, Jane Evanson, Sian Ellard, Ashley Grossman, Federico Roncaroli, Mônica R. Gadelha, Márta Korbonits, Amar Agha, Scott Akker, Elena Daniela Aflorei, Sándor Alföldi, Wiebke Arlt, Brew Atkinson, Anna Aulinas-Masó, Simon Aylwin, Philippe Backeljauw, Corin Badiu, Stephanie E Baldeweg, Gul Bano, Ariel Barkan, Julian Barwell, Carmen Bernal-González, G. M. Besser, John S. Bevan, Joanne Blair, Pierre Bouloux, Lisa Bradley, Michael Buchfelder, Mehtap Çakır, Natalie Canham, Paul Carroll, Harvinder Chahal, Tim Cheetham, F. Chentli, Richard N. Clayton, Mark L. Cohen, Trevor Cole, Hamish Courtney, Elizabeth Crowne, Daniel J. Cuthbertson, Jacob Dal, Nadezhda Dalantaeva, Christina Daousi, Ken Darzy, Mehul Dattani, Justin H. Davies, J.R. Davis, Margaret de Castro, Laura De Marinis, William Drake, Pinaki Dutta, Larisa Dzeranova, Britt Edén Engström, Rosalind A. Eeles, Maria Elfving, Marianne S. Elston, Louise Emmerson, Naomi Fersht, Simona Fica, Stefan Fischli, Daniel Flanagan, Maria Fleseriu, Pamela U. Freda, Theodore C. Friedman, Lawrence A. Frohman, Patricia Gallego, Evelien Gevers, Edit Gláz, James A. Goldman, Anthony P. Goldstone, Miklós Góth, Lynn Greenhalgh, Joan Grieve, Mirtha Guitelman, Alper Gürlek, Mark Gurnell, Katalin Horváth, Trevor A. Howlett, Charlotte Höybye, Steven Hunter, Donato Iacovazzo, Péter Igaz, Warrick J. Inder, Takeo Iwata, Louise Izatt, Sujatha Jagadeesh, Gregory Kaltsas, Felicity Kaplan, Niki Karavitaki, Darko Kaštelan, Michelle L. Katz, Tara Kearney, Bernard Khoo, Cathy Kiraly‐Borri
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
the DDD study, Nadia Akawi, Jeremy F. McRae, Morad Ansari, Meena Balasubramanian, Moira Blyth, Angela F. Brady, Stephen Clayton, Trevor Cole, Charu Deshpande, Tomas Fitzgerald, Nicola Foulds, Richard Francis, George C. Gabriel, Sebastian S. Gerety, Judith Goodship, Emma Hobson, Wendy D. Jones, Shelagh Joss, Daniel A. King, Nikolai Klena, Ajith Kumar, Melissa Lees, Chris Lelliott, Jenny Lord, Dominic McMullan, Mary O’Regan, Deborah Osio, Virginia Piombo, Elena Prigmore, Diana Rajan, Elisabeth Rosser, Alejandro Sifrim, Audrey Smith, G. Jawahar Swaminathan, Peter D. Turnpenny, James W. Whitworth, Caroline F. Wright, Helen V. Firth, Jeffrey C. Barrett, Cecilia Lo, David Fitzpatrick, Matthew E. Hurles