ScholarIQanswers from OpenAlex & ORCID
Hélène Dollfus
ResearcherPublications, citations & collaboration network
Hélène Dollfus is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Hélène Dollfus have?
ScholarIQindexed works
Hélène Dollfus has 373 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Hélène Dollfus have?
ScholarIQcitation count
Hélène Dollfus has 19,756 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Hélène Dollfus?
ScholarIQh-index
Hélène Dollfus has an h-index of 76 in OpenAlex.
What is the i10-index of Hélène Dollfus?
ScholarIQi10-index
Hélène Dollfus has an i10-index of 229 in OpenAlex.
What is the ORCID of Hélène Dollfus?
ScholarIQorcid
The ORCID for Hélène Dollfus is on the source record.
What is the OpenAlex record for Hélène Dollfus?
ScholarIQopenalex
The OpenAlex for Hélène Dollfus is on the source record.
What are the most-cited papers on Hélène Dollfus?
ScholarIQmost cited works
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, Julius O.B. Jacobsen, Daniel Daniš, Jean-Philippe F. Gourdine, Michael Gargano, Nomi L. Harris, Nicolas Matentzoglu, Julie A. McMurry, David Osumi-Sutherland, Valentina Cipriani, James P. Balhoff, Tom Conlin, Hannah Blau, Gareth Baynam, R. Palmer, Dylan Gratian, Hugh Dawkins, Michael M. Segal, Anna Jansen, Ahmed Muaz, Willie Chang, Jenna Bergerson, Stanley J. F. Laulederkind, Zafer Yüksel, Sergi Beltrán, Alexandra F. Freeman, Panagiotis I. Sergouniotis, Daniel W. Durkin, Andrea L. Storm, Marc Hanauer, Michael Brudno, Susan M. Bello, Murat Sincan, Kayli Rageth, Matthew T. Wheeler, Renske Oegema, Halima Lourghi, Maria G. Della Rocca, Rachel Thompson, F Castellanos, James R. Priest, Charlotte Cunningham‐Rundles, Ayushi Hegde, Ruth C. Lovering, Catherine Hajek, Annie Olry, Luigi D. Notarangelo, Morgan Similuk, Xingmin Zhang, David Gómez‐Andrés, Hanns Lochmüller, Hélène Dollfus, Sergio D. Rosenzweig, Shruti Marwaha, Ana Rath, Kathleen E. Sullivan, Cynthia L. Smith, Joshua D. Milner, Dorothée Leroux, Cornelius F. Boerkoel, Amy D. Klion, Melody C. Carter, Tudor Groza, Damian Smedley, Melissa Haendel, Chris Mungall, Peter N. Robinson
Retinal layer segmentation in multiple sclerosis: a systematic review and meta-analysis
Axel Petzold, Laura J. Balcer, Peter A. Calabresi, Fiona Costello, Teresa C. Frohman, Elliot M. Frohman, Elena H. Martínez‐Lapiscina, Ari Green, Randy H. Kardon, Olivier Outteryck, Friedemann Paul, Sven Schippling, P. Vermersch, Pablo Villoslada, Lisanne J. Balk, Orhan Aktaş, Philipp Albrecht, Jane Ashworth, Nasrin Asgari, Laura J. Balcer, Lisanne J. Balk, Graeme C. Black, Daniel Boehringer, Raed Behbehani, Leslie Benson, Robert Bermel, Jacqueline Bernard, Alexander U. Brandt, Jodie Burton, Peter A. Calabresi, Jonathan Calkwood, Christian Cordano, Fiona Costello, Ardith Courtney, Andrés Cruz-Herranz, Ricarda Diem, Avril Daly, Hélène Dollfus, Christina Fasser, Carsten Finke, Jette Lautrup Frederiksen, Elliot M. Frohman, Teresa C. Frohman, Elena García‐Martín, Inés González‐Suarez, Gorm Pihl-Jensen, Jennifer Graves, Ari Green, Joachim Havla, Bernhard Hemmer, Su‐Chun Huang, Jaime Imitola, Hong Jiang, David Keegan, Eric Kildebeck, Alexander Klistorner, Benjamin Knier, Scott Kolbe, Thomas Korn, Bart P. Leroy, Letizia Leocani, Dorothée Leroux, Netta Levin, Petra Lišková, Birgit Lorenz, Jana Lízrová Preiningerová, Elena H. Martínez‐Lapiscina, Janine Mikolajczak, Xavier Montalbán, Mark J. Morrow, Rachel Nolan, Timm Oberwahrenbrock, Frederike Cosima Oertel, Celia Oreja‐Guevara, Benjamin Osborne, Olivier Outteryck, Athina Papadopoulou, Friedemann Paul, Axel Petzold, Marius Ringelstein, Shiv Saidha, Bernardo Sánchez‐Dalmau, Jaume Sastre‐Garriga, Sven Schippling, Robert K. Shin, Neil Shuey, Kerstin Soelberg, Ahmed Toosy, R. Martinez Torres, Ángela Vidal‐Jordana, Pablo Villoslada, Amy Waldman, Owen White, Ann Ming Yeh, Sui H. Wong, Hanna Zimmermann
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
Moumita Chaki, Rannar Airik, Amiya K. Ghosh, Rachel H. Giles, Rui Chen, Gisela G. Slaats, Hui Wang, Toby W. Hurd, Weibin Zhou, Andrew Cluckey, Heon Yung Gee, Gokul Ramaswami, Chen‐Jei Hong, Bruce A. Hamilton, Igor Červenka, Ranjani Sri Ganji, Vı́tězslav Bryja, Heleen H. Arts, Jeroen van Reeuwijk, Machteld M. Oud, Stef J.F. Letteboer, Ronald Roepman, Hervé Husson, Oxana Ibraghimov‐Beskrovnaya, Takayuki Yasunaga, Gerd Walz, Lorraine Eley, John A. Sayer, Bernhard Schermer, Max C. Liebau, Thomas Benzing, Stéphanie Le Corre, Iain A. Drummond, Sabine Janssen, Susan J. Allen, S. Natarajan, John F. O’Toole, Massimo Attanasio, Sophie Saunier, Corinne Antignac, Robert K. Koenekoop, Huanan Ren, Irma López, Ahmet Nayır, Corinne Stoetzel, Hélène Dollfus, Rustin Massoudi, Joseph G. Gleeson, Sharon Andreoli, D Doherty, Anna Lindstrad, Christelle Golzio, Nicholas Katsanis, Lars Pape, Emad B. Abboud, Ali A. Al‐Rajhi, Richard A. Lewis, Heymut Omran, Eva Y.-H.P. Lee, Shaohui Wang, JoAnn Sekiguchi, Rudel A. Saunders, Colin A. Johnson, Elizabeth Garner, Katja Vanselow, Jens Andersen, Joseph Shlomai, Gudrun Nürnberg, Peter Nürnberg, Shawn Levy, Agata Smogorzewska, Edgar A. Otto, Friedhelm Hildebrandt
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
NISC Comparative Sequencing Program, Erica E. Davis, Qi Zhang, Qin Liu, Bill H. Diplas, Lisa Davey, Jane Hartley, Corinne Stoetzel, Katarzyna Szymańska, Gokul Ramaswami, Clare V. Logan, Donna M. Muzny, Alice Young, David A. Wheeler, Pedro Cruz, Margaret Morgan, Lora Lewis, Praveen F. Cherukuri, Baishali Maskeri, Nancy F. Hansen, James C. Mullikin, Robert W. Blakesley, Gerard G. Bouffard, Gàbor Gyapay, Susanne Rieger, Burkhard Tönshoff, Ilse Kern, Neveen A. Soliman, Thomas J. Neuhaus, Kathryn J. Swoboda, Hülya Kayserili, Tomas E Gallagher, Richard A. Lewis, Carsten Bergmann, Edgar A. Otto, Sophie Saunier, Peter Scambler, Philip L. Beales, Joseph G. Gleeson, Eamonn R. Maher, Tania Attié‐Bitach, Hélène Dollfus, Colin A. Johnson, Eric D. Green, Richard A. Gibbs, Friedhelm Hildebrandt, Eric A. Pierce, Nicholas Katsanis
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
Edgar A. Otto, Toby W. Hurd, Rannar Airik, Moumita Chaki, Weibin Zhou, Corinne Stoetzel, Suresh B. Patil, Shawn Levy, Amiya K. Ghosh, Carlos Murga‐Zamalloa, Jeroen van Reeuwijk, Stef J.F. Letteboer, Liyun Sang, Rachel H. Giles, Qin Liu, Karlien L. M. Coene, Alejandro Estrada‐Cuzcano, Rob W.J. Collin, Heather M. McLaughlin, Susanne Held, J. M. Kasanuki, Gokul Ramaswami, Jinny Conte, Irma López, Joseph Washburn, James W. MacDonald, Jinghua Hu, Yukiko Yamashita, Eamonn R. Maher, Lisa M. Guay‐Woodford, Hartmut P.H. Neumann, Nicholas Obermüller, Robert K. Koenekoop, Carsten Bergmann, Xiaoshu Bei, Richard A. Lewis, Nicholas Katsanis, Vanda S. Lopes, David S. Williams, Robert H. Lyons, Chi V. Dang, Daniela A. Brito, Mónica Bettencourt‐Dias, Xinmin Zhang, James D. Cavalcoli, Gudrun Nürnberg, Peter Nürnberg, Eric A. Pierce, Peter K. Jackson, Corinne Antignac, Sophie Saunier, Ronald Roepman, Hélène Dollfus, Hemant Khanna, Friedhelm Hildebrandt