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Helen Chapel

ResearcherPublications, citations & collaboration network

Helen Chapel is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Helen Chapel have?

ScholarIQindexed works

Helen Chapel has 227 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Helen Chapel have?

ScholarIQcitation count

Helen Chapel has 19,008 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Helen Chapel?

ScholarIQh-index

Helen Chapel has an h-index of 68 in OpenAlex.

What is the i10-index of Helen Chapel?

ScholarIQi10-index

Helen Chapel has an i10-index of 142 in OpenAlex.

What is the ORCID of Helen Chapel?

ScholarIQorcid

The ORCID for Helen Chapel is on the source record.

What is the OpenAlex record for Helen Chapel?

ScholarIQopenalex

The OpenAlex for Helen Chapel is on the source record.

What are the most-cited papers on Helen Chapel?

ScholarIQmost cited works
International Consensus Document (ICON): Common Variable Immunodeficiency Disorders
Francisco A. Bonilla, Işıl Barlan, Helen Chapel, Beatriz Tavares Costa‐Carvalho, Charlotte Cunningham‐Rundles, M. Teresa de la Morena, Francisco Espinosa‐Rosales, Lennart Hammarström, Shigeaki Nonoyama, Isabella Quinti, John M. Routes, Mimi L.K. Tang, Klaus Warnatz
The Journal of Allergy and Clinical Immunology In Practice. 2015870 CitationsOPEN ACCESS
Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans
Ulrich Salzer, Helen Chapel, A D Webster, Qiang Pan‐Hammarström, Annette Schmitt‐Graeff, Michael Schlesier, H. H. Peter, JK Rockstroh, Pascal Schneider, Alejandro A. Schäffer, Lennart Hammarström, Bodo Grimbacher
Nature Genetics. 2005675 Citations
The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
Markus G. Seidel, Gerhard Kindle, Benjamin Gathmann, Isabella Quinti, Matthew Buckland, Joris van Montfrans, Raphael Scheible, Stephan Rusch, Lukas Gasteiger, Bodo Grimbacher, Nizar Mahlaoui, Stephan Ehl, Mario Abinun, Michael H. Albert, Sarah Beaussant-Cohen, Jacinta Bustamante, Andrew J. Cant, Jean‐Laurent Casanova, Helen Chapel, Geneviève de Saint Basile, Esther de Vries, Inderjeet Dokal, Jean Donadieu, Anne Durandy, David Edgar, Teresa Español, Amos Etzioni, Alain Fischer, Bobby Gaspar, Richard A. Gatti, Andrew R. Gennery, Sofia Grigoriadou, Steven M. Holland, Gritta Janka, Maria Kanariou, Christoph Klein, Helen J. Lachmann, Desa Lilić, Ania Manson, N. Pascual Martínez, Isabelle Meyts, Nicolette Moes, Despina Moshous, Bénédicte Neven, Hans D. Ochs, Capucine Pïcard, Ellen D. Renner, Frédéric Rieux‐Laucat, Reinhard Seger, Annarosa Soresina, Dominique Stoppa‐Lyonnet, Vojtěch Thon, Adrian J. Thrasher, Frank L. van de Veerdonk, Anna Villa, Corry M.R. Weemaes, Klaus Warnatz, Beata M. Wolska, Shen-Yin Zhang
The Journal of Allergy and Clinical Immunology In Practice. 2019637 CitationsOPEN ACCESS
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor, Hilary C. Martin, Stefano Lise, John Broxholme, Jean‐Baptiste Cazier, Andy Rimmer, Alexander Kanapin, Gerton Lunter, Simon Fiddy, Chris Allan, A.R. Aricescu, Moustafa Attar, Christian Babbs, Jennifer Becq, David Beeson, Celeste Bento, P Bignell, Edward Blair, Veronica J. Buckle, Katherine R. Bull, Ondřej Cais, Holger Cario, Helen Chapel, Richard R. Copley, Richard J. Cornall, Jude Craft, Karin Dahan, Emma E. Davenport, Calliope A. Dendrou, Olivier Devuyst, Aimée L Fenwick, Jonathan Flint, Lars Fugger, Rodney D. Gilbert, Anne Goriely, Angie Green, Ingo H. Greger, Russell Grocock, Anja V. Gruszczyk, Robert Hastings, Edouard Hatton, Douglas R. Higgs, Adrian V. S. Hill, Chris Holmes, Malcolm F. Howard, Linda Hughes, Peter Humburg, David H. Johnson, Fredrik Karpe, Zoya Kingsbury, Usha Kini, Julian C. Knight, Jonathan Krohn, Sarah Lamble, Craig B. Langman, Lorne Lonie, Joshua Luck, Davis J. McCarthy, Simon J. McGowan, Mary Frances McMullin, Kerry A. Miller, Lisa Murray, Andrea H. Németh, M. Andrew Nesbit, David Nutt, Elizabeth Ormondroyd, Annette Oturai, Alistair T. Pagnamenta, Smita Y. Patel, Melanie J. Percy, Nayia Petousi, Paolo Piazza, Siân E. Piret, Guadalupe Polanco‐Echeverry, Niko Popitsch, Fiona Powrie, Christopher W. Pugh, Lynn Quek, Peter A. Robbins, Kathryn Robson, Alexandra Russo, Natasha Sahgal, Pauline A. van Schouwenburg, Anna Schuh, Earl D. Silverman, Alison Simmons, Per Soelberg Sørensen, Elizabeth Sweeney, John Taylor, Rajesh V. Thakker, Ian Tomlinson, Amy Trebes, Stephen R.F. Twigg, Holm H. Uhlig, Paresh Vyas, Tim J. Vyse, Steven A. Wall, Hugh Watkins, Michael P. Whyte, Lorna Witty
Nature Genetics. 2015393 CitationsOPEN ACCESS
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, Fabien Touzot, Nizar Mahlaoui, Fabian Hauck, Hirokazu Kanegane, Eduardo López‐Granados, Ester Mejstříková, Isabelle Pellier, Lionel Galicier, Claire Galambrun, Vincent Barlogis, Pierre Bordigoni, A Fourmaintraux, M. Hamidou, A. Dabadie, Françoise Le Deist, Filomeen Haerynck, O Marie, Pierre‐Simon Rohrlich, Jean‐Louis Stephan, Christelle Lenoir, Stéphanie Rigaud, Nathalie Lambert, Michèle Milili, Claudin Schiff, Helen Chapel, Capucine Pïcard, Geneviève de Saint Basile, Stéphane Blanche, Alain Fischer, Sylvain Latour
Blood. 2010366 CitationsOPEN ACCESS

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