Y. Gillerot

2.8k total citations
74 papers, 1.8k citations indexed

About

Y. Gillerot is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Y. Gillerot has authored 74 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 28 papers in Molecular Biology and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Y. Gillerot's work include Prenatal Screening and Diagnostics (13 papers), Congenital Anomalies and Fetal Surgery (9 papers) and Cleft Lip and Palate Research (8 papers). Y. Gillerot is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Congenital Anomalies and Fetal Surgery (9 papers) and Cleft Lip and Palate Research (8 papers). Y. Gillerot collaborates with scholars based in Belgium, France and Netherlands. Y. Gillerot's co-authors include Lionel Van Maldergem, L Koulischer, Alain Verloès, Catherine Fourneau, Eric Jauniaux, Christine Verellen‐Dumoulin, Olimpia Musumeci, A.J.M. Janssen, Helen Dolk and Miikka Vikkula and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Y. Gillerot

72 papers receiving 1.7k citations

Peers

Countries citing papers authored by Y. Gillerot

Since Specialization

Citations

This map shows the geographic impact of Y. Gillerot's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Y. Gillerot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Y. Gillerot more than expected).

Fields of papers citing papers by Y. Gillerot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Y. Gillerot. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Y. Gillerot. The network helps show where Y. Gillerot may publish in the future.

Co-authorship network of co-authors of Y. Gillerot

This figure shows the co-authorship network connecting the top 25 collaborators of Y. Gillerot. A scholar is included among the top collaborators of Y. Gillerot based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Y. Gillerot. Y. Gillerot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	External birth defects in southern Vietnam: a population-based study at the grassroots level of health care in Binh Thuan province 2013 ·BMC Pediatrics ·(unknown), Dung The Nguyen, (unknown), (unknown), Y. Gillerot, Raymond Reding, Annie Robert	18
2	IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign 2012 ·Data Archiving and Networked Services (DANS) ·(unknown), Michella Ghassibe‐Sabbagh, Nicole Revençu, Odile Boute, Melissa Lees, (unknown), C. Verellen‐Dumoulin, Yves Sznajer, Kathleen Claes, Koenraad Devriendt, (unknown), Geert Mortier, Catheline Vilain, Geneviève Pierquin, C. Vincent‐Delorme, Y. Gillerot, R Vanwijck, Bénédicte Bayet, Miikka Vikkula	1
3	Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E 2010 ·The American Journal of Human Genetics ·Eva Klopocki, Bianca P. Hennig, Katarina Dathe, Randi Koll, Thomy de Ravel, Emiel Baten, Eveline W Blom, Y. Gillerot, Johannes Weigel, Gabriele Krüger, Olaf Hiort, Petra Seemann, Stefan Mundlos	93
4	Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2 2009 ·The Journal of Pediatrics ·Arash Ghalamkarpour, Christian Debauche, Eric Haan, Nicole Van Regemorter, Yves Sznajer, (unknown), Nicole Revençu, Y. Gillerot, Laurence M. Boon, Miikka Vikkula	29
5	Partial proximal 10q trisomy: a new case associated with biliary atresia 2007 ·Hereditas ·Philippe A. Lysy, Catherine Sibille, Y. Gillerot, Françoise Smets, Étienne Sokal	9
6	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 2006 ·American Journal of Medical Genetics Part A ·Alain Verloès, Dominique Brémond‐Gignac, Bertrand Isidor, Albert David, Clarisse Baumann, M Leroy, René Stevens, Y. Gillerot, Delphine Héron, Bénédicte Héron, Brigitte Benzacken, Didier Lacombe, Han G. Brunner, Pierre Bitoun	52
7	Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population 2005 ·European Journal of Human Genetics ·Michella Ghassibe‐Sabbagh, Bénédicte Bayet, Nicole Revençu, Christine Verellen‐Dumoulin, Y. Gillerot, R Vanwijck, Miikka Vikkula	74
8	Hypophosphatasie de l'enfant : à propos d'un cas caractérisé par une nouvelle mutation 2004 ·Archives de Pédiatrie ·(unknown), Y. Gillerot, Étienne Mornet	5
9	Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test? 2001 ·European Journal of Human Genetics ·Alain Verloès, Y. Gillerot, Lionel Van Maldergem, Roland Schoos, Christian Herens, Mauricette Jamar, Vinciane Dideberg, (unknown), L Koulischer	37
10	Severe neonatal hypotonia: high prevalence of Prader-Willi syndrome, myotonic dystrophy and spinal muscular atrophy in a molecular prospective study. 2000 ·The American Journal of Human Genetics ·Lionel Van Maldergem, Peter Hilbert-Carius, Y. Gillerot	1
11	Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings 2000 ·European Journal of Pediatrics ·Lionel Van Maldergem, David Tuerlinckx, Ronald J. A. Wanders, Christine Vianey‐Saban, F. Van Hoof, J. J. Martin, Catherine Fourneau, Y. Gillerot, André Bachy	5
12	Syndrome of lipoatrophic diabetes, vitamin D resistant rickets, and persistent Müllerian ducts in a Turkish boy born to consanguineous parents 1996 ·American Journal of Medical Genetics ·Lionel Van Maldergem, (unknown), David Feldman, Roger Bouillon, (unknown), M. Dreyer, Rodolfo A. Rey, Cecilia Holm, Y. Gillerot	21
13	Morphological features of a case of retinoic acid embryopathy 1992 ·Prenatal Diagnosis ·Lionel Van Maldergem, Eric Jauniaux, Y. Gillerot	3
14	Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: Review and delineation of the Cerebro‐Acro‐Visceral Early lethality (CAVE) multiplex syndrome 1992 ·American Journal of Medical Genetics ·Alain Verloès, Y. Gillerot, Jean‐Paul Langhendries, Jean‐Pierre Fryns, L Koulischer	30
15	X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus 1991 ·Human Genetics ·(unknown), Marc Espeel, Frank Roels, Christine Petit, G. Dacremont, R. J. A. Wanders, Alain Verloès, Y. Gillerot	11
16	Mental retardation, short stature, almond‐shaped eyes, small downturned mouth and coned epiphyses: A new case of Hunter‐fraser syndrome 1990 ·American Journal of Medical Genetics ·Lionel Van Maldergem, Y. Gillerot, N. Perlmutter, (unknown), L Koulischer	1
17	Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance 1990 ·Clinical Genetics ·Lionel Van Maldergem, Y. Gillerot, (unknown), (unknown), L Koulischer	8
18	Tracheal agenesis: An exceptional cause of neonatal respiratory distress 1990 ·Pediatric Pulmonology ·Bénédicte Brichard, Eric Smeets, (unknown), Y. Gillerot, Oreste Battisti, Jean‐Paul Langhendries, Jean‐Marie Bertrand	4
19	La surveillance épidémiologique des anomalies congénitales par le registre EUROCAT. 1988 ·Revue d Épidémiologie et de Santé Publique ·Philippe De Wals, Helen Dolk, Françoise Bertrand, Y. Gillerot, (unknown), (unknown)	7
20	Leprechaunism (Donohue syndrome). A case with growth hormone deficiency. 1979 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Y. Gillerot, (unknown), J. Hustin	2

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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