Esther Vamos

773 citations

21 papers · 533 indexed · h-index 15

Co-authors: Nicole Van Regemorter Christine Devalck Pierre Heimann Eric Sariban Jiannis Ragoussis Frank Speleman Frances Flinter Angela Davies
Topics: Genomic variations and chromosomal abnormalities (5 papers)Genetics and Neurodevelopmental Disorders (3 papers)Acute Myeloid Leukemia Research (2 papers)
Cited by: Clinical Biochemistry Genetics Pediatrics, Perinatology and Child Health
Journals: The American Journal of Human Genetics Archives of Biochemistry and Biophysics Clinica Chimica Acta
Partner nations: Belgium United Kingdom United States

In The Last Decade

Esther Vamos

21 papers receiving 513 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization 2015 ·Journal of Molecular Diagnostics ·Daniel E. Sabath,M. A. Bender,Vijay G. Sankaran,Esther Vamos,Alex Kentsis,(unknown),Harvey A. Greisman	15
2	Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy 2005 ·The American Journal of Human Genetics ·Kazuhiko Nakabayashi,(unknown),Yan Ren,Ulpu Saarialho‐Kere,Nili Avidan,S. Gentles,Jeffrey R. MacDonald,Erik G. Puffenberger,Angela M. Christiano,Amalia Martı́nez-Mir,Julio C. Salas‐Alanís,Renata Rizzo,Esther Vamos,Anja Raams,Clifford Les,Eric Seboun,Nicolaas G.J. Jaspers,J. Beckmann,Charles E. Jackson,Stephen W. Scherer	55
3	Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy 2005 ·Human Genetics ·Sarah A. Shoichet,Laurence Duprez,(unknown),Vicki Waetzig,Corinna Menzel,Thomas Herdegen,Susann Schweiger,Bernard Dan,Esther Vamos,Hans‐Hilger Ropers,Vera M. Kalscheuer	31
4	Delineation of two distinct 6p deletion syndromes 1999 ·Human Genetics ·Angela Davies,Ghazala Mirza,Gurbax S. Sekhon,Peter D. Turnpenny,(unknown),Frank Speleman,(unknown),Nicole Van Regemorter,Esther Vamos,Frances Flinter,Jiannis Ragoussis	88
5	Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion 1998 ·Human Genetics ·Winnie Courtens,(unknown),(unknown),Ludwine Messiaen,Esther Vamos,(unknown),Dominique Haumont,(unknown),Anna Jauch,Joris Vermeesch,Frank Speleman	32
6	Alveolar soft‐part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25 1998 ·Genes Chromosomes and Cancer ·Pierre Heimann,Christine Devalck,(unknown),Eric Sariban,Esther Vamos	5
7	Alveolar soft-part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25 1998 ·Genes Chromosomes and Cancer ·Pierre Heimann,Christine Devalck,(unknown),Eric Sariban,Esther Vamos	67
8	Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome 1997 ·American Journal of Medical Genetics ·Winnie Courtens,Frank Speleman,Ludwine Messiaen,(unknown),Nadine Van Roy,Esther Vamos	16
9	A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome 1996 ·Human Genetics ·Angela Davies,Mark G. Olavesen,Richard Stephens,R Davidson,(unknown),Nicole Van Regemorter,Esther Vamos,Frances Flinter,(unknown),Jiannis Ragoussis	30
10	Cordocentesis for Rapid Karyotype: 421 Consecutive Cases 1995 ·Fetal Diagnosis and Therapy ·Catherine Donner,Françoise Rypens,(unknown),(unknown),(unknown),Nicole Van Regemorter,Esther Vamos,Freddy Avni,F Rodesch	16
11	Anaplastic large cell lymphoma of true histiocytic origin in an infant: Unusual clinical, hematological, and cytogenetic features 1994 ·Medical and Pediatric Oncology ·Alina Ferster,Francis Corazza,Pierre Heimann,(unknown),(unknown),Christine Devalck,Eric Sariban,Esther Vamos	3
12	Pyruvate dehydrogenase deficiency: Clinical and biochemical diagnosis 1993 ·Pediatric Neurology ·Linda De Meırleır,Willy Lissens,(unknown),(unknown),Alex Michotte,Jean‐Marie Brucher,Esther Vamos,Erik Gerlo,Inge Liebaers	46
13	Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the Elα subunit 1992 ·Human Genetics ·Linda De Meırleır,Willy Lissens,Esther Vamos,Inge Liebaers	16
14	Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings 1990 ·American Journal of Medical Genetics ·Serge Przedborski,Alina Ferster,Serge Goldman,(unknown),(unknown),T. Tønnesen,R. J. Pollitt,Esther Vamos	18
15	Value of glial fibrillary acidic protein determination in amniotic fluid for prenatal diagnosis of neural tube defects 1987 ·Clinica Chimica Acta ·Nicole Van Regemorter,J. Gheuens,M. Noppe,Esther Vamos,Mary J. Seller,Armand Löwenthal	11
16	Lethal osteopetrosis with multiple fractures in utero 1986 ·American Journal of Medical Genetics ·(unknown),D. Faverly,Esther Vamos,Nicole Van Regemorter,J Flament-Durand,(unknown),(unknown),John M. Opitz,James F. Reynolds	23
17	Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiency 1986 ·European Journal of Endocrinology ·(unknown),Ursula Kuhnle,(unknown),(unknown),Esther Vamos,Françoise Vertongen,(unknown),Decio Armanini	18
18	Leukemia in a trisomy 21 mosaic: Specific involvement of the trisomic cells 1986 ·Cancer Genetics and Cytogenetics ·Alina Ferster,Alain Verhest,Esther Vamos,(unknown),Jacques Otten	28
19	Fanconi's Anaemia. Simultaneous onset in 2 Siblings and unusual Cytological Findings 1982 ·Scandinavian Journal of Haematology ·Monique De Vroede,Walter Feremans,(unknown),(unknown),M. Toppet,Esther Vamos,Pierre Fondu	9
20	Thermodynamic analysis of purified human placental α-l-fucosidase 1979 ·Archives of Biochemistry and Biophysics ·Johan Hoebeke,José Groswasser,(unknown),Esther Vamos,A. Donny Strosberg	1

About Esther Vamos

Esther Vamos is a scholar working on Genetics, Biochemistry and Hematology, having authored 21 papers that have together received 533 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Acute Myeloid Leukemia Research (2 papers). The work is most often cited by research in Clinical Biochemistry (54 citations), Genetics (179 citations) and Pediatrics, Perinatology and Child Health (85 citations). Esther Vamos has collaborated with scholars based in Belgium, United Kingdom and United States. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, Archives of Biochemistry and Biophysics and Clinica Chimica Acta.

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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