ScholarIQanswers from OpenAlex & ORCID
Xavier Jeunemaı̂tre
ResearcherPublications, citations & collaboration network
Xavier Jeunemaı̂tre is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Xavier Jeunemaı̂tre have?
ScholarIQindexed works
Xavier Jeunemaı̂tre has 588 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Xavier Jeunemaı̂tre have?
ScholarIQcitation count
Xavier Jeunemaı̂tre has 34,970 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Xavier Jeunemaı̂tre?
ScholarIQh-index
Xavier Jeunemaı̂tre has an h-index of 92 in OpenAlex.
What is the i10-index of Xavier Jeunemaı̂tre?
ScholarIQi10-index
Xavier Jeunemaı̂tre has an i10-index of 306 in OpenAlex.
What is the ORCID of Xavier Jeunemaı̂tre?
ScholarIQorcid
The ORCID for Xavier Jeunemaı̂tre is on the source record.
What is the OpenAlex record for Xavier Jeunemaı̂tre?
ScholarIQopenalex
The OpenAlex for Xavier Jeunemaı̂tre is on the source record.
What are the most-cited papers on Xavier Jeunemaı̂tre?
ScholarIQmost cited works
The 2017 international classification of the Ehlers–Danlos syndromes
Fransiska Malfait, Clair A. Francomano, Peter H. Byers, John W. Belmont, Britta Berglund, James H. Black, Lara Bloom, Jessica Bowen, Angela F. Brady, Nigel Burrows, Marco Castori, Helen Cohen, Marina Colombi, Serwet Demirdas, Julie De Backer, Anne De Paepe, Sylvie Fournel‐Gigleux, Michael Frank, Neeti Ghali, Cecilia Giunta, Rodney Grahame, Alan J. Hakim, Xavier Jeunemaı̂tre, Diana Johnson, Birgit Juul‐Kristensen, Ines Kapferer‐Seebacher, Hanadi Kazkaz, Tomoki Kosho, Mark E. Lavallee, Howard P. Levy, Roberto Mendoza‐Londono, Melanie Pepin, F. Michael Pope, Eyal Reinstein, Leema Robert, Marianne Rohrbach, Lynn Sanders, Glenda Sobey, Tim Van Damme, Anthony Vandersteen, Caroline van Mourik, Nicol Voermans, Nigel Wheeldon, Johannes Zschocke, Brad T. Tinkle
First International Consensus on the diagnosis and management of fibromuscular dysplasia
Heather L. Gornik, Alexandre Persu, David Adlam, Lucas S. Aparicio, Michel Azizi, Marion Boulanger, Rosa María Bruno, Peter de Leeuw, Natalia Fendrikova-Mahlay, James B. Froehlich, Santhi K. Ganesh, Bruce Gray, Cathlin Jamison, Andrzej Januszewicz, Xavier Jeunemaı̂tre, Daniella Kadian‐Dodov, Esther SH Kim, Jason C. Kovacic, Pamela Mace, Alberto Morganti, Aditya Sharma, Andrew M. Southerland, Emmanuel Touzé, Patricia Van der Niepen, Ji‐Guang Wang, Ido Weinberg, Scott G. Wilson, Jeffrey W. Olin, Pierre-François Plouin
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
Juliette Albuisson, Swetha E. Murthy, Michael Bandell, Bertrand Coste, Hélène Louis-Dit-Picard, Jayanti Mathur, Madeleine Fénéant‐Thibault, G. Tertian, Jean-Pierre de Jaureguiberry, Pierre-Yves Syfuss, Stuart M. Cahalan, Loïc Garçon, Fabienne Toutain, Pierre‐Simon Rohrlich, J. Delaunay, Véronique Picard, Xavier Jeunemaı̂tre, Ardem Patapoutian
Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome
Peter H. Byers, John W. Belmont, James H. Black, Julie De Backer, Michael Frank, Xavier Jeunemaı̂tre, Diana Johnson, Melanie Pepin, Leema Robert, Lynn Sanders, Nigel Wheeldon
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, Stéphanie Miserey‐Lenkei, Nabila Bouatia‐Naji, Olena Pylypenko, Geneviève Beaurain, Amélie Bonnefond, Olivier Sand, Christophe Simian, Emmanuelle Vidal‐Petiot, Christelle Soukaseum, Chantal Mandet, Françoise Broux, Olivier Chabre, Michel Delahousse, Vincent Esnault, B. Fiquet, Pascal Houillier, Corinne Isnard Bagnis, Jens Koenig, Martin Konrad, Paul Landais, Chebel Mourani, Patrick Niaudet, Vincent Probst, Christel Thauvin, Robert J. Unwin, Steven D. Soroka, Georg Ehret, Stephan Ossowski, Mark J. Caulfield, Patrick Bruneval, Xavier Estivill, Philippe Froguel, Juliette Hadchouel, Jean‐Jacques Schott, Xavier Jeunemaı̂tre