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David Cheillan

ResearcherPublications, citations & collaboration network

David Cheillan is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does David Cheillan have?

ScholarIQindexed works

David Cheillan has 142 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does David Cheillan have?

ScholarIQcitation count

David Cheillan has 4,293 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of David Cheillan?

ScholarIQh-index

David Cheillan has an h-index of 35 in OpenAlex.

What is the i10-index of David Cheillan?

ScholarIQi10-index

David Cheillan has an i10-index of 66 in OpenAlex.

What is the ORCID of David Cheillan?

ScholarIQorcid

The ORCID for David Cheillan is on the source record.

What is the OpenAlex record for David Cheillan?

ScholarIQopenalex

The OpenAlex for David Cheillan is on the source record.

What are the most-cited papers on David Cheillan?

ScholarIQmost cited works
Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project
David McHugh, Cynthia A. Cameron, José E. Abdenur, Mahera Abdulrahman, Ona O. Adair, Shahira Ahmed Al Nuaimi, Henrik Åhlman, Jennifer J. Allen, I. Antonozzi, Shaina Archer, Sylvia Mann Au, Christiane Auray‐Blais, Mei Baker, Fiona Bamforth, Kinga Beckmann, Gessi Bentz Pino, Stanton L. Berberich, Robert Binard, François Boemer, Jim Bonham, Nancy N. Breen, Sandra C. Bryant, Michele Caggana, S. Graham Caldwell, Marta Camilot, Carlene Campbell, Claudia Carducci, Rohit Cariappa, Clover Carlisle, Ubaldo Caruso, Michela Cassanello, Ane Miren Castilla, Daisy E. Castiñeiras Ramos, Pranesh Chakraborty, Ram Chandrasekar, Alfredo Chardon Ramos, David Cheillan, Yin‐Hsiu Chien, Thomas A. Childs, Petr Chrastina, Yuri Cleverthon Sica, José Ángel Cocho de Juan, Maria Elena Colandre, Veronica Cornejo Espinoza, Gaetano Corso, Robert J. Currier, Denis Cyr, Noémi Czuczy, Oceania D’Apolito, Tim D. Davis, Monique G. de Sain-van der Velden, Carmen lgado De Pecellin, Iole Maria Di Gangi, Cristina Maria Di Stefano, Yannis Dotsikas, Melanie Downing, Stephen M. Downs, Bonifacio Dy, Mark Dymerski, Inmaculada Rueda, Bert Elvers, Roger B. Eaton, Barbara M. Eckerd, Fatma El‐Mougy, Sarah Eroh, Mercedes Espada, Catherine Evans, Sandy Fawbush, Kristel F. Fijolek, Lawrence Fisher, Leifur Franzson, Dianne M. Frazier, Luciana R.C. Garcia, Maria Sierra García-Valdecasas Bermejo, Dimitar Gavrilov, Rosemarie Gerace, Giuseppe Giordano, Yolanda González Irazabal, Lawrence Greed, Robert E. Grier, Elyse Grycki, Xuefan Gu, Fizza Gulamali-Majid, Arthur F. Hagar, Lianshu Han, W. Harry Hannon, Christa Haslip, Fayza Abdelhamid Hassan, Miao He, Amy Hietala, Leslie Himstedt, Gary Hoffman, William H. Hoffman, Philis Hoggatt, Patrick V. Hopkins, David M. Hougaard, Kerie Hughes, Patricia Hunt, Wuh‐Liang Hwu, June Hynes
Genetics in Medicine. 2011353 CitationsOPEN ACCESS
Creatine biosynthesis and transport in health and disease
Marie Joncquel-Chevalier Curt, Pia‐Manuela Voicu, Monique Fontaine, Anne‐Frédérique Dessein, Nicole Porchet, Karine Mention-Mulliez, Dries Dobbelaere, Gustavo Soto‐Ares, David Cheillan, Jòseph Vamecq
Biochimie. 2015240 Citations
Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010
J.G. Loeber, Dimitris Platis, Rolf Zetterström, Shlomo Almashanu, François Boemer, James R. Bonham, Patricia Borde, Ian Brincat, David Cheillan, Eugènie Dekkers, Dobry Dimitrov, Ralph Fingerhut, Leifur Franzson, Urh Grošelj, David M. Hougaard, Mária Knapková, Mirjana Kočova, Vjosa Kotori, Viktor Kožich, A. Kremezna, Riikka Kurkijärvi, Giancarlo la Marca, Ruth Mikelsaar, Tatjana Milenković, V. M. Mit'kin, Florentina Moldovanu, Uta Ceglarek, Loretta O’Grady, Mariusz Ołtarzewski, Rolf D. Pettersen, Danijela Petković Ramadža, Damilya Salimbayeva, Mira Samardžić, Markhabo Shamsiddinova, Jurgita Songailienė, Ildikó Szatmári, Nazi Tabatadze, Başak Tezel, Alma Toromanović, Irina Tovmasyan, Natalia Uşurelu, Pārsla Vēvere, Laura Vilarinho, Marios Vogazianos, Raquel Yahyaoui, Maximilian Zeyda, Peter C. J. I. Schielen
International Journal of Neonatal Screening. 2021240 CitationsOPEN ACCESS
TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation
François Foulquier, Mustapha Amyere, Jaak Jaeken, Renate Zeevaert, Els Schollen, Valérie Race, Riet Bammens, Willy Morelle, Claire Rosnoblet, Dominique Legrand, Didier Demaegd, Neil R.M. Buist, David Cheillan, Nathalie Guffon, Pierre Morsomme, Willem Annaert, Hudson H. Freeze, Emile Van Schaftingen, Miikka Vikkula, Gert Matthijs
The American Journal of Human Genetics. 2012206 CitationsOPEN ACCESS
Phenotype and genotype in 101 males with X-linked creatine transporter deficiency
Jiddeke M. van de Kamp, Ofir T. Betsalel, Saadet Mercimek‐Mahmutoglu, Lara Abulhoul, Stephanie Grünewald, Irina Anselm, Hatem Azzouz, Drago Bratkovic, Arjan de Brouwer, Ben C.J. Hamel, Tjitske Kleefstra, Helger G. Yntema, Jaume Campistol, Marta Vilaseca, David Cheillan, Marc D’Hooghe, Luísa Diogo, Paula Garcia, Carla Valongo, Maria José Fonseca, Suzanna G.M. Frints, Bridget Wilcken, Sigrun von der Haar, Hanne Meijers‐Heijboer, Floris C. Hofstede, Diana Johnson, Sarina G. Kant, Laurence Lion‐François, G. Pitelet, Nicola Longo, J A Maat-Kievit, João Monteiro, Arnold Münnich, Ania C. Muntau, Marie‐Cécile Nassogne, Hitoshi Osaka, Katrin Õunap, Jean-Marc Pinard, Susana Quijano‐Roy, Imke Poggenburg, Nicola Poplawski, Omar Abdul‐Rahman, Antònia Ribes, Ángela Arias, Joy Yaplito‐Lee, Andreas Schulze, Charles E. Schwartz, Susanne Schwenger, G. Soares, Yves Sznajer, Vassili Valayannopoulos, Hilde Van Esch, Stephan Waltz, Mirjam M. C. Wamelink, Petra J. W. Pouwels, Abdellatif Errami, Marjo S. van der Knaap, C. Jakobs, Grazia M.S. Mancini, Gajja S. Salomons
Journal of Medical Genetics. 2013167 CitationsOPEN ACCESS

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