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E. Vámos

Sex chromosome abnormalities after intracytoplasmic sperm injection
1995 · I Liebaers, StantonF Hoegerman, et al. · The Lancet · 168
Amyotrophic lateral sclerosis mutant vesicle-associated membrane protein-associated protein-B transgenic mice develop TAR-DNA-binding protein-43 pathology
2010 · E.L. Tudor, C.M. Galtrey, et al. · Neuroscience · 90
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies
1994 · W. Courtens, M. B. Petersen, et al. · American Journal of Medical Genetics · 89
Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.
1994 · M J Abramowicz, M Andrien, et al. · Journal of Clinical Investigation · 85
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Congenital malformations in 10,000 consecutive births in a university hospital: Need for genetic counseling and prenatal diagnosis
1984 · N. Van Regemorter, J. Dodion, et al. · The Journal of Pediatrics · 52
Acrocallosal syndrome in Algerian boy born to consanguineous parents: Review of the literature and further delineation of the syndrome
1997 · W. Courtens, E. Vamos, et al. · American Journal of Medical Genetics · 40
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome
1991 · G. Pierquin, N. Van Regemorter, et al. · Human Genetics · 38
Moebius syndrome in an infant exposed in utero to benzodiazepines
1992 · W. Courtens, E. Vamos, et al. · The Journal of Pediatrics · 34
Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factor.
1992 · B Vandamme, W Lissens, et al. · PubMed · 30
Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly
1998 · W. Courtens, W. Tjalma, et al. · American Journal of Medical Genetics · 25
Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer.
1995 · K Amfo, B Neyns, et al. · PubMed · 20
Partial trisomy 3p in two siblings: Clinical and pathological findings
1983 · N. Van Regemorter, E. Vamos, et al. · European Journal of Pediatrics · 18
Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14.
1988 · A Verhest, R Heimann, et al. · PubMed · 13
Granulocytic sarcoma showing chromosomal changes other than the t(8;21)
1994 · P. Heimann, E. Vamos, et al. · Cancer Genetics and Cytogenetics · 12
Prenatal diagnosis and fetal pathology of partial trisomy 20p–monosomy 4p resulting from paternal translocation
1985 · E. Vamos, D. Pratola, et al. · Prenatal Diagnosis · 12
Assessment of an electron‐impact GC‐MS method for organic acids and glycine conjugates in amniotic fluid
2004 · A. Kumps, E. Vamos, et al. · Journal of Inherited Metabolic Disease · 11
Pyruvate dehydrogenase deficiency due to a mutation of the E1 α subunit
1991 · L. J. de Meirleir, W. Lissens, et al. · Journal of Inherited Metabolic Disease · 10
Unusual early manifestation of multiple sulfatase deficiency.
1981 · N Perlmutter-Cremer, J Libert, et al. · PubMed · 10
Alphafetoprotein (AFP), concanavalin A non-reactive AFP and specific acetylcholinesterase in amniotic fluid from pathological pregnancies. Predictive values for open spina bifida
1983 · N. van Regemorter, V. Defleur, et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 6
CHARGE association in a neonate exposed in utero to carbon monoxide.
1996 · W Courtens, Y Hennequin, et al. · PubMed · 5
Pathological Pregnancies: Results of amniotic fluid studies and fetal outcome
1986 · N. Van Regemorter, E. Vamos, et al. · Acta Obstetricia Et Gynecologica Scandinavica · 5
On the ?red? character of a mutant of Newcastle Disease Virus (NDV)
1966 · Elie Vamos · Archives of Virology · 4
[Medical genetics service].
2002 · G Vassart, M Abramowicz, et al. · PubMed · 2
[Bone marrow graft in hereditary diseases].
1992 · W Bujan, A Ferster, et al. · PubMed · 1
[Collection of fetal cord blood for karyotyping].
1992 · C Donner, F Avni, et al. · PubMed · 1
Works count: 35
Citation count: 784
H-index: 13
I10-index: 18
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