Esther Vamos

773 citations

21 papers · 533 indexed · h-index 15

Clinical Biochemistry top 10%
Genetics top 10%
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 3
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 2
Biochemistry
Molecular Biology
- Biochemical and Molecular Research 2
Hematology
- Acute Myeloid Leukemia Research 2
Cardiology and Cardiovascular Medicine
- Cardiac tumors and thrombi 2
Pulmonary and Respiratory Medicine
- Sarcoma Diagnosis and Treatment 2
Plant Science
- Chromosomal and Genetic Variations 2

Co-authors: Nicole Van Regemorter Christine Devalck Pierre Heimann Eric Sariban Jiannis Ragoussis Frank Speleman Frances Flinter Angela Davies
Cited by: Clinical Biochemistry Genetics Pediatrics, Perinatology and Child Health
Journals: The American Journal of Human Genetics (1 paper)Archives of Biochemistry and Biophysics (1 paper)Clinica Chimica Acta (1 paper)
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

The 25 scholars most cited alongside Esther Vamos, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Esther Vamos Line = papers co-authored together Esther Vamos links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization Journal of Molecular Diagnostics ·Daniel E. Sabath,M. A. Bender,Vijay G. Sankaran,Esther Vamos,Alex Kentsis,Hye-Son Yi,Harvey A. Greisman	2015	15
2	Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy The American Journal of Human Genetics ·Kazuhiko Nakabayashi,Daniela Amann,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	2005	55
3	Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy Human Genetics ·Sarah A. Shoichet,Laurence Duprez,Olivier Hagens,Vicki Waetzig,Corinna Menzel,Thomas Herdegen,Susann Schweiger,Bernard Dan,Esther Vamos,Hans‐Hilger Ropers,Vera M. Kalscheuer	2005	31
4	Delineation of two distinct 6p deletion syndromes Human Genetics ·Angela Davies,Ghazala Mirza,Gurbax S. Sekhon,Peter D. Turnpenny,Frank Leroy,Frank Speleman,Caroline Law,Nicole Van Regemorter,Esther Vamos,Frances Flinter,Jiannis Ragoussis	1999	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 Human Genetics ·Winnie Courtens,Dominique Grossman,Nadine Van Roy,Ludwine Messiaen,Esther Vamos,Veronique Toppet,Dominique Haumont,Catherine Streydio,Anna Jauch,Joris Vermeesch,Frank Speleman	1998	32
6	Alveolar soft‐part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25 Genes Chromosomes and Cancer ·Pierre Heimann,Christine Devalck,C. Debusscher,Eric Sariban,Esther Vamos	1998	5
7	Alveolar soft-part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25 Genes Chromosomes and Cancer ·Pierre Heimann,Christine Devalck,C. Debusscher,Eric Sariban,Esther Vamos	1998	67
8	Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome American Journal of Medical Genetics ·Winnie Courtens,Frank Speleman,Ludwine Messiaen,Jeannie Bormans,Nadine Van Roy,Esther Vamos	1997	16
9	A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome Human Genetics ·Angela Davies,Mark G. Olavesen,Richard Stephens,R Davidson,Daniele Delneste,Nicole Van Regemorter,Esther Vamos,Frances Flinter,Iman Abusaad,Jiannis Ragoussis	1996	30
10	Cordocentesis for Rapid Karyotype: 421 Consecutive Cases Fetal Diagnosis and Therapy ·Catherine Donner,Françoise Rypens,Vincent Paquet,Eddie Cohen,Danielle Delneste,Nicole Van Regemorter,Esther Vamos,Freddy Avni,F Rodesch	1995	16
11	Anaplastic large cell lymphoma of true histiocytic origin in an infant: Unusual clinical, hematological, and cytogenetic features Medical and Pediatric Oncology ·Alina Ferster,Francis Corazza,Pierre Heimann,Marie‐Françoise Dehou,C. De Busscher,Christine Devalck,Eric Sariban,Esther Vamos	1994	3
12	Pyruvate dehydrogenase deficiency: Clinical and biochemical diagnosis Pediatric Neurology ·Linda De Meırleır,Willy Lissens,Robert Denis,Jean-Louis Wayenberg,Alex Michotte,Jean‐Marie Brucher,Esther Vamos,Erik Gerlo,Inge Liebaers	1993	46
13	Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the Elα subunit Human Genetics ·Linda De Meırleır,Willy Lissens,Esther Vamos,Inge Liebaers	1992	16
14	Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings American Journal of Medical Genetics ·Serge Przedborski,Alina Ferster,Serge Goldman,Renee Adrienne Wolter,Micheline Song,T. Tønnesen,R. J. Pollitt,Esther Vamos	1990	18
15	Value of glial fibrillary acidic protein determination in amniotic fluid for prenatal diagnosis of neural tube defects Clinica Chimica Acta ·Nicole Van Regemorter,J. Gheuens,M. Noppe,Esther Vamos,Mary J. Seller,Armand Löwenthal	1987	11
16	Lethal osteopetrosis with multiple fractures in utero American Journal of Medical Genetics ·N. El Khazen,D. Faverly,Esther Vamos,Nicole Van Regemorter,J Flament-Durand,Brigitte Carton,Noémi Cremer‐Perlmutter,John M. Opitz,James F. Reynolds	1986	23
17	Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiency European Journal of Endocrinology ·Danièle Bosson,Ursula Kuhnle,Nicole Mees,Joseph Ramet,Esther Vamos,Françoise Vertongen,Renee Adrienne Wolter,Decio Armanini	1986	18
18	Leukemia in a trisomy 21 mosaic: Specific involvement of the trisomic cells Cancer Genetics and Cytogenetics ·Alina Ferster,Alain Verhest,Esther Vamos,Emilie De Maertelaere,Jacques Otten	1986	28
19	Fanconi's Anaemia. Simultaneous onset in 2 Siblings and unusual Cytological Findings Scandinavian Journal of Haematology ·Monique De Vroede,Walter Feremans,Emilie de Maertelaere‐Laurent,Israël Mandelbaum,M. Toppet,Esther Vamos,Pierre Fondu	1982	9
20	Thermodynamic analysis of purified human placental α-l-fucosidase Archives of Biochemistry and Biophysics ·Johan Hoebeke,José Groswasser,Nelly Bousard,Esther Vamos,A. Donny Strosberg	1979	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), Acute Myeloid Leukemia Research (2 papers), Cardiac tumors and thrombi (2 papers), Biochemical and Molecular Research (2 papers), Prenatal Screening and Diagnostics (2 papers), Sarcoma Diagnosis and Treatment (2 papers) and Chromosomal and Genetic Variations (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.

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