Yves Sznajer

4.2k total citations
50 papers, 1.1k citations indexed

About

Yves Sznajer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Yves Sznajer has authored 50 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Genetics and 11 papers in Surgery. Recurrent topics in Yves Sznajer's work include Genomic variations and chromosomal abnormalities (7 papers), Galectins and Cancer Biology (7 papers) and Protein Tyrosine Phosphatases (6 papers). Yves Sznajer is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Galectins and Cancer Biology (7 papers) and Protein Tyrosine Phosphatases (6 papers). Yves Sznajer collaborates with scholars based in Belgium, France and United Kingdom. Yves Sznajer's co-authors include Clarisse Baumann, Alain Verloès, Françoise Meire, Hélène Cavé, Marc Abramowicz, Valérie Cormier‐Daire, Marc Schrooyen, Julie Désir, Sarah Smithson and Fanny Depasse and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Yves Sznajer

50 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Yves Sznajer Belgium	19	623	373	186	156	136	50	1.1k
Maria Iascone Italy	20	608 1.0×	320 0.9×	265 1.4×	106 0.7×	105 0.8×	115	1.5k
Monika Goś Poland	19	769 1.2×	331 0.9×	97 0.5×	77 0.5×	74 0.5×	49	1.2k
Sumita Danda India	16	489 0.8×	269 0.7×	70 0.4×	196 1.3×	88 0.6×	122	1.0k
Kirmo Wartiovaara Finland	17	1.0k 1.7×	260 0.7×	249 1.3×	94 0.6×	108 0.8×	38	1.4k
Vijitha Puviindran Canada	15	1.1k 1.8×	586 1.6×	103 0.6×	226 1.4×	58 0.4×	24	1.7k
Nara Sobreira United States	19	690 1.1×	671 1.8×	113 0.6×	56 0.4×	103 0.8×	61	1.3k
Ariana Kariminejad Iran	21	756 1.2×	715 1.9×	207 1.1×	64 0.4×	60 0.4×	100	1.5k
Salim Aftimos New Zealand	19	812 1.3×	690 1.8×	253 1.4×	52 0.3×	89 0.7×	72	1.5k
Michael H. Guo United States	20	603 1.0×	509 1.4×	70 0.4×	170 1.1×	84 0.6×	33	1.2k
Guilherme Lopes Yamamoto Brazil	18	732 1.2×	469 1.3×	271 1.5×	72 0.5×	51 0.4×	57	1.3k

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

Biard, Jean‐Marc, Philippe Clapuyt, Catherine Barréa, et al.. (2021). 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. European Journal of Medical Genetics. 64(4). 104189–104189. 9 indexed citations

Hanseeuw, Bernard, Laurence Dricot, Lisa Quenon, et al.. (2020). Defining a Centiloid scale threshold predicting long-term progression to dementia in patients attending the memory clinic: an [18F] flutemetamol amyloid PET study. European Journal of Nuclear Medicine and Molecular Imaging. 48(1). 302–310. 47 indexed citations

Wiame, Elsa, Naïma Deggouj, Antonella Boschi, et al.. (2017). Childhood hearing loss is a key feature of CAPOS syndrome: A case report. International Journal of Pediatric Otorhinolaryngology. 104. 191–194. 7 indexed citations

Bergh, Peter Van den, Yves Sznajer, Ron A. Wevers, et al.. (2017). A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy. Neuromuscular Disorders. 27(11). 1043–1046. 7 indexed citations

Urquhart, Jill, R. C. Roberts, Stavit A. Shalev, et al.. (2016). Exploring the genetic basis of 3MC syndrome: Findings in 12 further families. American Journal of Medical Genetics Part A. 170(5). 1216–1224. 22 indexed citations

Beleza‐Meireles, Ana, Catheline Hocq, Philippe Clapuyt, et al.. (2016). “Serpentine-like syndrome”–A very rare multiple malformation syndrome characterised by brachioesophagus and vertebral anomalies. European Journal of Medical Genetics. 60(2). 100–104. 4 indexed citations

Giehl, Kathrin, Thomas Herzinger, Hans Wolff, et al.. (2015). Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability. Acta Dermato Venereologica. 96(4). 468–472. 13 indexed citations

Ghassibe‐Sabbagh, Michella, Nicole Revençu, Odile Boute, et al.. (2012). IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign. Data Archiving and Networked Services (DANS). 59. 1 indexed citations

Vergult, Sarah, A. Jeannette M. Hoogeboom, Emilia K. Bijlsma, et al.. (2012). Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients. Genetics in Medicine. 15(3). 195–202. 22 indexed citations

10.

Huybrechts, Sophie, Corinne De Laet, Patrick Bontems, et al.. (2011). Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype. JIMD Reports. 4. 103–108. 31 indexed citations

11.

Désir, Julie, Yves Sznajer, Fanny Depasse, et al.. (2010). LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma. European Journal of Human Genetics. 18(7). 761–767. 75 indexed citations

12.

Ghalamkarpour, Arash, Christian Debauche, Eric Haan, et al.. (2009). Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2. The Journal of Pediatrics. 155(1). 90–93. 29 indexed citations

13.

Calado, Joaquim, Yves Sznajer, Daniel L. Metzger, et al.. (2008). Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. Nephrology Dialysis Transplantation. 23(12). 3874–3879. 78 indexed citations

14.

Aeby, Alec, Yves Sznajer, Hélène Cavé, et al.. (2007). Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q(10) deficiency. Ghent University Academic Bibliography (Ghent University). 2 indexed citations

15.

Sznajer, Yves, H. Annika Siitonen, Gaia Roversi, et al.. (2007). Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes. European Journal of Pediatrics. 167(2). 175–181. 14 indexed citations

16.

Sznajer, Yves, Stanislas Lyonnet, Monique Elmaleh, et al.. (2007). Familial CHARGE syndrome because of CHD7 mutation: clinical intra‐ and interfamilial variability. Clinical Genetics. 72(2). 112–121. 59 indexed citations

17.

Deconinck, Nicolas, France Ziereisen, Hazim Kadhim, et al.. (2007). Metachromatic leukodystrophy without arylsulfatase A deficiency: A new case of saposin-B deficiency. European Journal of Paediatric Neurology. 12(1). 46–50. 37 indexed citations

18.

Sznajer, Yves, Boris Keren, Clarisse Baumann, et al.. (2007). The Spectrum of Cardiac Anomalies in Noonan Syndrome as a Result of Mutations in the PTPN11 Gene. PEDIATRICS. 119(6). e1325–e1331. 71 indexed citations

19.

Devriendt, Koenraad, Eric Legius, Yves Sznajer, et al.. (2005). Syndromic clefting : broadening the clinical spectrum of an “old” syndrome, confirmation of a rare syndrome and description of a novel entity. 16(1). 211–212. 2 indexed citations

20.

Sznajer, Yves, Clarisse Baumann, Albert David, et al.. (2003). Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome). European Journal of Pediatrics. 162(12). 863–867. 51 indexed citations

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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