Esther Vamos

773 total citations
21 papers, 533 citations indexed

About

Esther Vamos is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Esther Vamos has authored 21 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Surgery. Recurrent topics in Esther Vamos's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Acute Myeloid Leukemia Research (2 papers). Esther Vamos is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Acute Myeloid Leukemia Research (2 papers). Esther Vamos collaborates with scholars based in Belgium, United Kingdom and United States. Esther Vamos's co-authors include Nicole Van Regemorter, Christine Devalck, Pierre Heimann, Eric Sariban, Jiannis Ragoussis, Frank Speleman, Frances Flinter, Angela Davies, Linda De Meırleır and Willy Lissens and has published in prestigious journals such as The American Journal of Human Genetics, Archives of Biochemistry and Biophysics and Clinica Chimica Acta.

In The Last Decade

Esther Vamos

21 papers receiving 513 citations

Peers

Esther Vamos

GENET

PRM

PPCH

Patricia L. Monteleone United States

Shogo Minamikawa Japan

Naoya Morisada Japan

J. W. E. Oorthuys Netherlands

Tomoyasu Higashimoto United States

María Juliana Ballesta‐Martínez Spain

R J Desnick United States

E. Vámos Belgium

Raymon Vijzelaar Netherlands

Eden Haverfield United States

Patricia L. Monteleone United States

Esther Vamos

147 ×0.5

96 ×0.5

GENET

44 ×0.5

PRM

69 ×0.8

PPCH

24 ×0.4

Citations per year, relative to Esther Vamos Esther Vamos (= 1×) peers Patricia L. Monteleone

Countries citing papers authored by Esther Vamos

Since Specialization

Citations

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

Fields of papers citing papers by Esther Vamos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Vamos

This figure shows the co-authorship network connecting the top 25 collaborators of Esther Vamos. A scholar is included among the top collaborators of Esther Vamos 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 Esther Vamos. Esther Vamos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sabath, Daniel E., M. A. Bender, Vijay G. Sankaran, et al.. (2015). Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization. Journal of Molecular Diagnostics. 18(1). 92–99. 15 indexed citations

Nakabayashi, Kazuhiko, Yan Ren, Ulpu Saarialho‐Kere, et al.. (2005). Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy. The American Journal of Human Genetics. 76(3). 510–516. 55 indexed citations

Shoichet, Sarah A., Laurence Duprez, Vicki Waetzig, et al.. (2005). Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy. Human Genetics. 118(5). 559–567. 31 indexed citations

Davies, Angela, Ghazala Mirza, Gurbax S. Sekhon, et al.. (1999). Delineation of two distinct 6p deletion syndromes. Human Genetics. 104(1). 64–72. 88 indexed citations

Courtens, Winnie, Ludwine Messiaen, Esther Vamos, et al.. (1998). Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion. Human Genetics. 103(4). 497–505. 32 indexed citations

Heimann, Pierre, et al.. (1998). Alveolar soft‐part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25. Genes Chromosomes and Cancer. 23(2). 194–197. 5 indexed citations

Heimann, Pierre, et al.. (1998). Alveolar soft-part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25. Genes Chromosomes and Cancer. 23(2). 194–197. 67 indexed citations

Courtens, Winnie, et al.. (1997). Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome. American Journal of Medical Genetics. 71(4). 479–485. 16 indexed citations

Davies, Angela, Mark G. Olavesen, Richard Stephens, et al.. (1996). A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome. Human Genetics. 98(4). 454–459. 30 indexed citations

10.

Donner, Catherine, Françoise Rypens, Nicole Van Regemorter, et al.. (1995). Cordocentesis for Rapid Karyotype: 421 Consecutive Cases. Fetal Diagnosis and Therapy. 10(3). 192–199. 16 indexed citations

11.

Ferster, Alina, Francis Corazza, Pierre Heimann, et al.. (1994). Anaplastic large cell lymphoma of true histiocytic origin in an infant: Unusual clinical, hematological, and cytogenetic features. Medical and Pediatric Oncology. 22(2). 147–152. 3 indexed citations

12.

Meırleır, Linda De, Willy Lissens, Alex Michotte, et al.. (1993). Pyruvate dehydrogenase deficiency: Clinical and biochemical diagnosis. Pediatric Neurology. 9(3). 216–220. 46 indexed citations

13.

Meırleır, Linda De, Willy Lissens, Esther Vamos, & Inge Liebaers. (1992). Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the Elα subunit. Human Genetics. 88(6). 649–652. 16 indexed citations

14.

Przedborski, Serge, Alina Ferster, Serge Goldman, et al.. (1990). Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings. American Journal of Medical Genetics. 35(4). 566–573. 18 indexed citations

15.

Regemorter, Nicole Van, J. Gheuens, M. Noppe, et al.. (1987). Value of glial fibrillary acidic protein determination in amniotic fluid for prenatal diagnosis of neural tube defects. Clinica Chimica Acta. 165(1). 83–88. 11 indexed citations

16.

Faverly, D., Esther Vamos, Nicole Van Regemorter, et al.. (1986). Lethal osteopetrosis with multiple fractures in utero. American Journal of Medical Genetics. 23(3). 811–819. 23 indexed citations

17.

Kuhnle, Ursula, et al.. (1986). Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiency. European Journal of Endocrinology. 113(4_Suppl). S376–S380. 18 indexed citations

18.

Ferster, Alina, et al.. (1986). Leukemia in a trisomy 21 mosaic: Specific involvement of the trisomic cells. Cancer Genetics and Cytogenetics. 20(1-2). 109–113. 28 indexed citations

19.

Vroede, Monique De, et al.. (1982). Fanconi's Anaemia. Simultaneous onset in 2 Siblings and unusual Cytological Findings. Scandinavian Journal of Haematology. 28(5). 431–440. 9 indexed citations

20.

Hoebeke, Johan, et al.. (1979). Thermodynamic analysis of purified human placental α-l-fucosidase. Archives of Biochemistry and Biophysics. 198(2). 556–561. 1 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.

Explore authors with similar magnitude of impact