On this page:OverviewPublicationsKey papers
ScholarIQanswers from OpenAlex & ORCID

Jill Clayton‐Smith

ResearcherPublications, citations & collaboration network

Jill Clayton‐Smith is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Jill Clayton‐Smith have?

ScholarIQindexed works

Jill Clayton‐Smith has 376 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Jill Clayton‐Smith have?

ScholarIQcitation count

Jill Clayton‐Smith has 28,190 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Jill Clayton‐Smith?

ScholarIQh-index

Jill Clayton‐Smith has an h-index of 94 in OpenAlex.

What is the i10-index of Jill Clayton‐Smith?

ScholarIQi10-index

Jill Clayton‐Smith has an i10-index of 258 in OpenAlex.

What is the ORCID of Jill Clayton‐Smith?

ScholarIQorcid

The ORCID for Jill Clayton‐Smith is on the source record.

What is the OpenAlex record for Jill Clayton‐Smith?

ScholarIQopenalex

The OpenAlex for Jill Clayton‐Smith is on the source record.

What are the most-cited papers on Jill Clayton‐Smith?

ScholarIQmost cited works
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations
Matteo M. Guerrini, Cristina Sobacchi, Barbara Cassani, Mario Abinun, Sara Şebnem Kılıç, Alessandra Pangrazio, Daniele Moratto, Evelina Mazzolari, Jill Clayton‐Smith, Paul J. Orchard, Fraser P. Coxon, Miep Helfrich, Julie C. Crockett, David Mellis, Ashok Vellodi, İlhan Tezcan, Luigi D. Notarangelo, Michael J. Rogers, Paolo Vezzoni, Anna Villa, Annalisa Frattini
The American Journal of Human Genetics. 2008307 CitationsOPEN ACCESS
Spectrum of <i>MLL2</i> (<i>ALR</i>) mutations in 110 cases of Kabuki syndrome
Mark Hannibal, Kati J. Buckingham, Sarah Ng, Jeffrey E. Ming, Anita E. Beck, Margaret J. McMillin, Heidi Gildersleeve, Abigail W. Bigham, Holly K. Tabor, Heather C. Mefford, Joseph Cook, Koh‐ichiro Yoshiura, Tadashi Matsumoto, Naomichi Matsumoto, Noriko Miyake, Hidefumi Tonoki, Kenji Naritomi, Tadashi Kaname, Toshiro Nagai, Hirofumi Ohashi, Kenji Kurosawa, Jia‐Woei Hou, Tohru Ohta, Deshung Liang, Akira Sudo, Colleen A. Morris, Siddharth Banka, Graeme C. Black, Jill Clayton‐Smith, Deborah A. Nickerson, Elaine H. Zackai, Tamim H. Shaikh, Dian Donnai, Norio Niikawa, Jay Shendure, Michael J. Bamshad
American Journal of Medical Genetics Part A. 2011196 CitationsOPEN ACCESS
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
Morad Ansari, Gemma Poke, Quentin R. V. Ferry, Kathleen A. Williamson, Roland Christopher Lochore Aldridge, Alison Meynert, Hemant Bengani, Cheng Yee Chan, Hülya Kayserili, Şahin Avcı, Raoul C. M. Hennekam, Anne Katrin Lampe, E. Redeker, Tessa Homfray, Alison Ross, Marie Falkenberg Smeland, Sahar Mansour, Michael Parker, Jacqueline Cook, Miranda Splitt, Richard B. Fisher, Alan Fryer, Alex Magee, Andrew O.M. Wilkie, Angela Barnicoat, Angela F. Brady, Nicola Cooper, Catherine Mercer, Charu Deshpande, Christopher Bennett, Daniela T. Pilz, Deborah Ruddy, Deirdre Cilliers, Diana Johnson, Dragana Josifova, Elisabeth Rosser, Elizabeth M. Thompson, Emma Wakeling, Esther Kinning, Fiona Stewart, Frances Flinter, Katta M. Girisha, Helen Cox, Helen V. Firth, Helen Kingston, Jamie S Wee, Jane A. Hurst, Jill Clayton‐Smith, John Tolmie, Julie Vogt, Katrina Tatton‐Brown, Kate Chandler, Katrina Prescott, Louise C. Wilson, Mahdiyeh Behnam, Meriel McEntagart, Rosemarie Davidson, Sally Ann Lynch, Sanjay M. Sisodiya, Sarju Mehta, Shane McKee, Shehla Mohammed, Simon Holden, Soo-Mi Park, Susan Holder, Victoria Harrison, Vivienne McConnell, Wayne Lam, Andrew Green, Dian Donnai, Maria Bitner‐Glindzicz, Deirdre E. Donnelly, Christoffer Nellåker, Martin S. Taylor, David Fitzpatrick
Journal of Medical Genetics. 2014172 CitationsOPEN ACCESS
LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome
Yun Li, Barbara Pawlik, Nursel Elçioğlu, Mona Aglan, Hülya Kayserili, Gökhan Yigit, E. Ferda Perçin, Frances R. Goodman, Gudrun Nürnberg, Asım Cenani, Jill Urquhart, Boi-Dinh Chung, Samira Ismail, Khalda Amr, Ayça Dilruba Aslanger, Christian Becker, Christian Netzer, Peter Scambler, Wafaa Eyaid, Hanan Hamamy, Jill Clayton‐Smith, Raoul C. M. Hennekam, Peter Nürnberg, Joachim Herz, Samia A. Temtamy, Bernd Wollnik
The American Journal of Human Genetics. 2010169 CitationsOPEN ACCESS

Related on ScholarIQ

470M+ articles · free account