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Yves Gillerot

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Truong Hoang; Dung The Nguyen; Phuong Van Ngoc Nguyen; Raymond Reding; Yves Gillerot; Dong A Tran; Annie Robert
External birth defects in southern Vietnam: a population-based study at the grassroots level of health care in Binh Thuan province.
Brian P Kelley; Fransiska Malfait; Luisa Bonafe; Dustin Baldridge; Erica Homan; Sofie Symoens; Andy Willaert; Nursel Elcioglu; Lionel Van Maldergem; Christine Verellen-Dumoulin; Yves Gillerot; Dobrawa Napierala; Deborah Krakow; Peter Beighton; andrea superti-furga; Anne De Paepe; Brendan Lee
Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome.
Eva Klopocki; Bianca P Hennig; Katarina Dathe; Randi Koll; Thomy de Ravel; Emiel Baten; Eveline Blom; Yves Gillerot; Johannes F W Weigel; Gabriele Krüger; Olaf Hiort; Petra Seemann; Stefan Mundlos
Deletion and point mutations of PTHLH cause brachydactyly type E.

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All Publications

2013: Truong Hoang; Dung The Nguyen; Phuong Van Ngoc Nguyen; Raymond Reding; Yves Gillerot; Dong A Tran; Annie Robert
External birth defects in southern Vietnam: a population-based study at the grassroots level of health care in Binh Thuan province.
BMC pediatrics 2013;13():67.
2011: Brian P Kelley; Fransiska Malfait; Luisa Bonafe; Dustin Baldridge; Erica Homan; Sofie Symoens; Andy Willaert; Nursel Elcioglu; Lionel Van Maldergem; Christine Verellen-Dumoulin; Yves Gillerot; Dobrawa Napierala; Deborah Krakow; Peter Beighton; andrea superti-furga; Anne De Paepe; Brendan Lee
Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2011;26(3):666-72.
2010: Eva Klopocki; Bianca P Hennig; Katarina Dathe; Randi Koll; Thomy de Ravel; Emiel Baten; Eveline Blom; Yves Gillerot; Johannes F W Weigel; Gabriele Krüger; Olaf Hiort; Petra Seemann; Stefan Mundlos
Deletion and point mutations of PTHLH cause brachydactyly type E.
American journal of human genetics 2010;86(3):434-9.
2009: Arash Ghalamkarpour; Christian Debauche; Eric Haan; Nicole Van Regemorter; Yves Sznajer; Dominique Thomas; Nicole Revencu; Yves Gillerot; Laurence M Boon; Miikka Vikkula
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2.
The Journal of pediatrics 2009;155(1):90-3.
2008: Anne-Frédérique Minsart; Anne Van Onderbergen; Francotte Jacques; Crener Kurt; Yves Gillerot
Indication of prenatal diagnosis in pregnancies complicated by undetectable second-trimester maternal serum estriol levels.
Journal of prenatal medicine 2008;2(3):27-30.
2007: Philippe Lysy; Catherine Sibille; Yves Gillerot; Françoise Smets; Etienne M Sokal
Partial proximal 10q trisomy: a new case associated with biliary atresia.
Hereditas 2007;144(5):191-4.
2006: Alain Verloes; Dominique Bremond-Gignac; Bertrand Isidor; Albert David; Clarisse Baumann; Marie-Anne Leroy; René Stevens; Yves Gillerot; Delphine Héron; Bénédicte Héron; Brigitte Benzacken; Didier Lacombe; Han Brunner; Pierre Bitoun
Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinical classification of the so-called Ohdo syndrome, and delineation of two new BMR syndromes, one X-linked and one autosomal recessive.
American journal of medical genetics. Part A 2006;140(12):1285-96.
2006: Lionel Van Maldergem; H Annika Siitonen; Nadine Jalkh; Eliane Chouery; M De Roy; Valérie Delague; M Muenke; Ethylin Jabs; J Cai; L L Wang; S E Plon; C Fourneau; Marjo Kestilä; Yves Gillerot; André Mégarbané; Alain Verloes
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene.
Journal of medical genetics 2006;43(2):148-52.
2006: Michella Ghassibe; Benedicte Bayet; Nicole Revencu; L Desmyter; Christine Verellen-Dumoulin; Yves Gillerot; Naima Deggouj; Romain Vanwijck; Miikka Vikkula
Orofacial clefting: update on the role of genetics.
B-ENT 2006;2 Suppl 4():20-4.
2005: Michella Ghassibé; Benedicte Bayet; Nicole Revencu; Christine Verellen-Dumoulin; Yves Gillerot; Romain Vanwijck; Miikka Vikkula
Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.
European journal of human genetics : EJHG 2005;13(11):1239-42.
2005: K Rack; André Delannoy; C Ravoet; P Vannuffel; J Hamels; Yves Gillerot
Translocation of BCL2 and BCL6 to the same immunoglobulin heavy chain locus in a case of follicular lymphoma.
Leukemia & lymphoma 2005;46(10):1513-6.
2005: A Destree; C Fourneau; C Dugauquier; Sonia Rombout; Daniel Sartenaer; Yves Gillerot
Prenatal diagnosis of trisomy 6 mosaicism.
Prenatal diagnosis 2005;25(5):354-7.
2005: Ester Garne; Maria Loane; Helen Dolk; Catherine de Vigan; Gioacchino Scarano; D Tucker; Claude Stoll; Blanca Gener; Anna Pierini; Vera Nelen; C Rösch; Yves Gillerot; Maria Feijoo; R Tincheva; Annette Queisser-Luft; Marie-Claude Addor; C Mosquera; Miriam Gatt; Barisic ingeborg
Prenatal diagnosis of severe structural congenital malformations in Europe.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2005;25(1):6-11.
2004: Ester Garne; Maria Loane; Catherine de Vigan; Gioacchino Scarano; H E K de Walle; Yves Gillerot; Claude Stoll; Marie-Claude Addor; David Stone; Blanca Gener; Maria Feijoo; Carmen Mosquera-Tenreiro; Miriam Gatt; Annette Queisser-Luft; Neus Baena; Helen Dolk
Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe.
Prenatal diagnosis 2004;24(11):908-12.
2004: Sonia Rombout; Daniel Sartenaer; Benoît Parmentier; Christian Dugauquier; Yves Gillerot
A rare case of de novo distal 19q trisomy prenatally diagnosed.
Prenatal diagnosis 2004;24(10):822-7.
2004: Michella Ghassibé; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.
Journal of medical genetics 2004;41(2):e15.
2003: Michella Ghassibe; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Gene symbol: IRF6. Disease: Van der Woude syndrome.
Human genetics 2003;113(6):558.
2003: Michella Ghassibe; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Gene symbol IRF6. Disease: Van der Woude syndrome and popliteal pterygium.
Human genetics 2003;113(6):558.
2003: Michella Ghassibe; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Gene symbol: IRF6. Disease: Van der Woude syndrome.
Human genetics 2003;113(6):558.
2003: Michella Ghassibe; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Gene symbol: IRF6. Disease: Van der Woude syndrome.
Human genetics 2003;113(6):557.
2003: Michella Ghassibe; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Gene symbol: IRF6. Disease: Van der Woude syndrome.
Human genetics 2003;113(6):557.
2003: Michella Ghassibe; Nicole Revencu; Benedicte Bayet; Yves Gillerot; Romain Vanwijck; Christine Verellen-Dumoulin; Miikka Vikkula
Gene symbol: IRF6. Disease: Van der Woude syndrome.
Human genetics 2003;113(6):556.
2002: Lionel Van Maldergem; Frans Trijbels; Salvatore DiMauro; Pavel Sindelar; Olimpia Musumeci; Antoon Janssen; Xavier Delberghe; Jean-Jacques Martin; Yves Gillerot
Coenzyme Q-responsive Leigh's encephalopathy in two sisters.
Annals of neurology 2002;52(6):750-4.
2002: Nicole Laporte; Guillaume Sébire; Yves Gillerot; Renzo Guerrini; Sophie Ghariani
Cognitive epilepsy: ADHD related to focal EEG discharges.
Pediatric neurology 2002;27(4):307-11.
2002: S Andries; Daniel Sartenaer; K Rack; Sonia Rombout; D Tuerlinckx; Yves Gillerot; Lionel Van Maldergem
Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly.
Journal of medical genetics 2002;39(10):E60.
2001: Elfride De Baere; M J Dixon; Kent W Small; Ethylin Jabs; Bart P Leroy; koenraad devriendt; Yves Gillerot; Geert R Mortier; Françoise Meire; Lionel Van Maldergem; Winnie Courtens; Helle Hjalgrim; S Huang; I Liebaers; Nicole Van Regemorter; P Touraine; V Praphanphoj; Alain Verloes; Nitin Udar; V Yellore; Meenal Chalukya; Svetlana Yelchits; Anne De Paepe; Frédérique Kuttenn; Marc Fellous; Reiner A Veitia; Ludwine MESSIAEN
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation.
Human molecular genetics 2001;10(15):1591-600.
2001: Alain Verloes; Yves Gillerot; Lionel Van Maldergem; Roland Schoos; Christian Herens; Mauricette Jamar; Vinciane Dideberg; S Lesenfants; L Koulischer
Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?
European journal of human genetics : EJHG 2001;9(1):1-4.
2000: E S Silva; S Lumbroso; M Medina; Yves Gillerot; C Sultan; Etienne M Sokal
Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis.
Journal of hepatology 2000;32(1):154-8.
2000: Lionel Van Maldergem; D Tuerlinckx; R J Wanders; Christine Vianey-Saban; F Van Hoof; J J Martin; C Fourneau; Yves Gillerot; ALAIN BACHY
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings.
European journal of pediatrics 2000;159(1-2):108-12.
1997: Yves Gillerot; C Fourneau; T Willems; Lionel Van Maldergem
Lethal femoral-facial syndrome: a case with unusual manifestations.
Journal of medical genetics 1997;34(6):518-9.