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St Mary's Hospital

InstitutionResearch output, impact & collaborations

St Mary's Hospital is a institution indexed in ScholarIQ from OpenAlex.

What is known about St Mary's Hospital?

ScholarIQrecord summary

St Mary's Hospital is a research organisation in Manchester, GB. OpenAlex records 4,925 works and 572,198 citations for it. 738 researchers list it as their most recent affiliation.

How many works does St Mary's Hospital have?

ScholarIQindexed works

St Mary's Hospital has 4,925 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does St Mary's Hospital have?

ScholarIQcitation count

St Mary's Hospital has 572,198 citations in the OpenAlex counts ScholarIQ stores.

How many researchers are at St Mary's Hospital?

ScholarIQresearcher count

St Mary's Hospital has 738 researchers in the ScholarIQ index.

What is the average h-index at St Mary's Hospital?

ScholarIQavg h-index

St Mary's Hospital has an average h-index of 83 in OpenAlex.

What is the ROR of St Mary's Hospital?

ScholarIQror

The ROR for St Mary's Hospital is on the source record.

What is the OpenAlex record for St Mary's Hospital?

ScholarIQopenalex

The OpenAlex for St Mary's Hospital is on the source record.

Who are the most-cited researchers behind St Mary's Hospital?

ScholarIQtop researchers by citations
1
Jill Clayton‐Smith · Genomic variations and chromosomal abnormalities
376 works28,190 citations
2
John Aplin · Reproductive System and Pregnancy
522 works17,279 citations

What are the most-cited papers on St Mary's Hospital?

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

How much of the research on St Mary's Hospital is open access?

ScholarIQopen access share
100%OPEN ACCESS
Gold
0%
Green
25%
Hybrid
25%
Bronze
50%
Closed
0%

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