Yves Sznajer

4.2k citations

50 papers · 1.1k indexed · h-index 19

Co-authors: Clarisse Baumann Alain Verloès Hélène Cavé Françoise Meire Marc Abramowicz Valérie Cormier‐Daire Marc Schrooyen Julie Désir
Topics: Genomic variations and chromosomal abnormalities (7 papers)Galectins and Cancer Biology (7 papers)Protein Tyrosine Phosphatases (6 papers)
Cited by: Genetics Molecular Biology
Journals: SHILAP Revista de lepidopterologíaPEDIATRICS The American Journal of Human Genetics
Partner nations: Belgium France United Kingdom

In The Last Decade

Yves Sznajer

50 papers receiving 1.1k citations

Peers

Countries citing papers authored by Yves Sznajer

Since Specialization

Citations

This map shows the geographic impact of Yves Sznajer'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 Yves Sznajer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yves Sznajer more than expected).

Fields of papers citing papers by Yves Sznajer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yves Sznajer. 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 Yves Sznajer. The network helps show where Yves Sznajer may publish in the future.

Co-authorship network of co-authors of Yves Sznajer

This figure shows the co-authorship network connecting the top 25 collaborators of Yves Sznajer. A scholar is included among the top collaborators of Yves Sznajer 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 Yves Sznajer. Yves Sznajer 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	Antenatal diagnosis of CHARGE syndrome: Prenatal ultrasound findings and crucial role of fetal dysmorphic signs. About a series of 10 cases and review of literature 2021 ·European Journal of Medical Genetics ·Jean‐Marc Biard,(unknown),Philippe Clapuyt,Catherine Barréa,Valérie Benoît,Paméla Baldin,Pierre Bernard,(unknown),Yves Sznajer	9
2	Defining a Centiloid scale threshold predicting long-term progression to dementia in patients attending the memory clinic: an [18F] flutemetamol amyloid PET study 2020 ·European Journal of Nuclear Medicine and Molecular Imaging ·Bernard Hanseeuw,(unknown),Laurence Dricot,Lisa Quenon,Yves Sznajer,Jiří Cerman,John L. Woodard,Christopher Buckley,Gill Farrar,Adrian Ivanoiu,Renaud Lhommel	47
3	Antenatal diagnosis of cardio-facio-cutaneous syndrome: Prenatal characteristics and contribution of fetal facial dysmorphic signs in utero. About a case and review of literature 2019 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Jean‐Marc Biard,(unknown),Pierre Bernard,Valérie Race,Yves Sznajer	7
4	Patient with confirmed leopard syndrome developing multiple myeloma 2018 ·Dermatology Practical & Conceptual ·(unknown),(unknown),Liliane Marot,Gert Matthijs,Yves Sznajer,(unknown),Isabelle Tromme	5
5	Familial Forms of Cushing Syndrome in Primary Pigmented Nodular Adrenocortical Disease Presenting with Short Stature and Insidious Symptoms: A Clinical Series 2018 ·Hormone Research in Paediatrics ·(unknown),(unknown),Étienne Marbaix,Selda Aydın,Konstanze Hörtnagel,Sarah Lechner,Yves Sznajer,Véronique Beauloye,Dominique Maiter,Philippe A. Lysy	5
6	Childhood hearing loss is a key feature of CAPOS syndrome: A case report 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown),Elsa Wiame,Naïma Deggouj,Antonella Boschi,Romolo Daniele De Siati,Yves Sznajer,Marie‐Cécile Nassogne	7
7	“Serpentine-like syndrome”–A very rare multiple malformation syndrome characterised by brachioesophagus and vertebral anomalies 2016 ·European Journal of Medical Genetics ·Ana Beleza‐Meireles,(unknown),Catheline Hocq,Philippe Clapuyt,Pierre Bernard,Christian Debauche,Yves Sznajer	4
8	Exploring the genetic basis of 3MC syndrome: Findings in 12 further families 2016 ·American Journal of Medical Genetics Part A ·Jill Urquhart,R. C. Roberts,(unknown),Stavit A. Shalev,(unknown),Sheela Nampoothiri,Yves Sznajer,Nicole Revençu,(unknown),Mohnish Suri,Jamie M. Ellingford,Simon G. Williams,Sanjeev S. Bhaskar,Jill Clayton‐Smith	22
9	Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability 2015 ·Acta Dermato Venereologica ·Kathrin Giehl,Thomas Herzinger,Hans Wolff,Miklós Sárdy,Tanja von Braunmühl,(unknown),Yves Sznajer,Dominique Tennstedt,(unknown),Stefan Rapprich,Nicola Wagner,Regina C. Betz,Markus Braun‐Falco,Tim M. Strom,Thomas Ruzicka,Gertrud Eckstein	13
10	The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects 2015 ·American Journal of Medical Genetics Part A ·(unknown),Jacoba Louw,Jeroen Breckpot,Bert Callewaert,Catherine Barréa,Yves Sznajer,Marc Gewillig,Erika Souche,Luc Dehaspe,Joris Vermeesch,Diether Lambrechts,Koenraad Devriendt,Anniek Corveleyn	36
11	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
12	Autosomal insertional translocation mimicking an X-linked mode of inheritance 2012 ·European Journal of Medical Genetics ·(unknown),Olivier Pichon,(unknown),(unknown),Yves Sznajer,Albert David,Cédric Le Caignec	4
13	LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma 2010 ·European Journal of Human Genetics ·Julie Désir,Yves Sznajer,Fanny Depasse,(unknown),Marc Schrooyen,Françoise Meire,Marc Abramowicz	75
14	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
15	Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion 2008 ·Nephrology Dialysis Transplantation ·Joaquim Calado,Yves Sznajer,Daniel L. Metzger,Ana Rita,Marie C. Hogan,Antonios Kattamis,(unknown),Velibor Tasić,Johann Greil,Florian Brinkert,Markus J. Kemper,René Santer	78
16	Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q(10) deficiency 2007 ·Ghent University Academic Bibliography (Ghent University) ·Alec Aeby,Yves Sznajer,Hélène Cavé,E. Rebuffat,Rudy Van Coster,Odile Rigal,Patrick Van Bogaert	2
17	Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes 2007 ·European Journal of Pediatrics ·Yves Sznajer,H. Annika Siitonen,Gaia Roversi,(unknown),M. Scaillon,France Ziereisen,Sylvie Tenoutasse,Marjo Kestilä,Lidia Larizza	14
18	Metachromatic leukodystrophy without arylsulfatase A deficiency: A new case of saposin-B deficiency 2007 ·European Journal of Paediatric Neurology ·Nicolas Deconinck,(unknown),France Ziereisen,Hazim Kadhim,Yves Sznajer,Karine Pelc,Marie‐Cécile Nassogne,Marie T. Vanier,Bernard Dan	37
19	Syndromic clefting : broadening the clinical spectrum of an “old” syndrome, confirmation of a rare syndrome and description of a novel entity 2005 ·Koenraad Devriendt,(unknown),Eric Legius,Yves Sznajer,Jean‐Pierre Fryns,Miikka Vikkula,Trine Prescott	2
20	Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome) 2003 ·European Journal of Pediatrics ·Yves Sznajer,Clarisse Baumann,Albert David,Hubert Journel,Didier Lacombe,Yves Pérel,Pascale Blouin,(unknown),Jean‐Pierre Cézard,Michel Peuchmaur,(unknown),Inderjeet Dokal,Alain Verloès	51

About Yves Sznajer

Yves Sznajer is a scholar working on Genetics, Genetics and Cell Biology, having authored 50 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Galectins and Cancer Biology (7 papers) and Protein Tyrosine Phosphatases (6 papers). The work is most often cited by research in Genetics (373 citations), Genetics (106 citations) and Molecular Biology (623 citations). Yves Sznajer has collaborated with scholars based in Belgium, France and United Kingdom. Frequent co-authors include Clarisse Baumann, Alain Verloès, Hélène Cavé, Françoise Meire, Marc Abramowicz, Valérie Cormier‐Daire, Marc Schrooyen, Julie Désir, Sarah Smithson and David Geneviève. Their work appears in journals such as SHILAP Revista de lepidopterología, PEDIATRICS and The American Journal of Human Genetics.

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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