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J. Feingold · SciRah

Researcher profile · Semantic Scholar

J. Feingold

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J. Feingold — researcher profile on SciRah

h-index: 51
Works: 271
Citations: 8,856

Most-cited papers

Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis.
S. Marrakchi, P. Guigue, B. Renshaw, A. Puel +26 more
2011New England Journal of Medicine923 citations Open access
Semantic Scholar
Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression
F. Mochel, P. Charles, F. Seguin, J. Barritault +9 more
2007PLoS ONE245 citations Open access
Semantic Scholar
Estimating prevalence in single-gene kidney diseases progressing to renal failure.
Micheline Levy, J. Feingold
2000Kidney International226 citations Open access
Semantic Scholar
Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.
M. Leboyer, A. Philippe, M. Bouvard, M. Guilloud-Bataille +5 more
1999Biological Psychiatry205 citations
Semantic Scholar
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.
A. Philippe, M. Martinez, M. Guilloud-Bataille, C. Gillberg +10 more
1999Human Molecular Genetics185 citations
Semantic Scholar
Clinical homogeneity and genetic heterogeneity in Weill–Marchesani syndrome
L. Faivre, H. Dollfus, S. Lyonnet, Y. Alembik +8 more
2003American Journal of Medical Genetics. Part A149 citations
Semantic Scholar
Agenesis of corpus callosum: prenatal diagnosis and prognosis
M. Moutard, V. Kieffer, J. Feingold, F. Kieffer +7 more
2003Child's Nervous System147 citations
Semantic Scholar
Acute clinical events in 299 homozygous sickle cell patients living in France
Maria Grazia Neonato, M. Guilloud‐Bataille, P. Beauvais, P. Bégué +9 more
2000European Journal of Haematology135 citations
Semantic Scholar
Identifying modifier genes of monogenic disease: strategies and difficulties
E. Génin, J. Feingold, F. Clerget-Darpoux
2008Human Genetics124 citations Open access
Semantic Scholar
Long-term outcome of presymptomatic testing in Huntington disease
M. Gargiulo, S. Lejeune, M. Tanguy, K. Lahlou-Laforêt +4 more
2009European Journal of Human Genetics112 citations Open access
Semantic Scholar
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25‐q31
S. Baulac, F. Picard, Alexandra Herman, J. Feingold +6 more
2001Annals of Neurology102 citations Open access
Semantic Scholar
EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy)-- descriptive characteristics.
F. Kauffmann, M. Dizier, I. Annesi-Maesano, Jean Bousquet +15 more
1999Clinical and Experimental Allergy97 citations
Semantic Scholar
Female predominance and transmission distortion in the long-QT syndrome.
M. Imboden, H. Swan, I. Denjoy, I. M. van Langen +11 more
2006New England Journal of Medicine92 citations Open access
Semantic Scholar
A locus for simple pure febrile seizures maps to chromosome 6q22-q24.
R. Nabbout, J. Prud'homme, Alexandra Herman, J. Feingold +3 more
2002Brain : a journal of neurology91 citations
Semantic Scholar
Screening of OPTN in French familial amyotrophic lateral sclerosis.
S. Millecamps, S. Boillée, E. Chabrol, W. Camu +14 more
2011Neurobiology of Aging85 citations
Semantic Scholar
Isolated corpus callosum agenesis: a ten‐year follow‐up after prenatal diagnosis (How are the children without corpus callosum at 10 years of age?)
M. Moutard, V. Kieffer, J. Feingold, F. Lewin +6 more
2012Prenatal Diagnosis84 citations
Semantic Scholar
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.
M. Tazir, H. Azzedine, S. Assami, P. Sindou +8 more
2004Brain : a journal of neurology83 citations
Semantic Scholar
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience
P. Charron, D. Heron, M. Gargiulo, P. Richard +8 more
2002Journal of Medical Genetics81 citations Open access
Semantic Scholar
Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis.
S. Monnot, David C. Samuels, L. Hesters, N. Frydman +11 more
2013Human Molecular Genetics75 citations Open access
Semantic Scholar
Phenotypic variability at the TGF-β1 locus in Camurati-Engelmann disease
A. Campos‐Xavier, J. Saraiva, R. Savarirayan, A. Verloes +5 more
2001Human Genetics71 citations
Semantic Scholar
The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis
M. Gabolde, D. Hubert, M. Guilloud‐Bataille, C. Lenaerts +2 more
2001Journal of Medical Genetics70 citations Open access
Semantic Scholar
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections
M. Neonato, Yong-Lu Chang, M. Guilloud‐Bataille, C. Lapouméroulie +7 more
1999European Journal of Human Genetics63 citations
Semantic Scholar
rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration
J. Zerbib, J. Seddon, F. Richard, Robyn C. Reynolds +9 more
2009PLoS ONE60 citations Open access
Semantic Scholar
Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations.
C. Cazeneuve, Zaruhi Hovannesyan, D. Geneviève, H. Hayrapetyan +7 more
2003Arthritis & Rheumatism56 citations
Semantic Scholar
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16.
N. Sylvius, F. Tesson, C. Gayet, P. Charron +8 more
2001American Journal of Human Genetics55 citations Open access
Semantic Scholar
Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy
F. Cartault, P. Munier, Edgar Benko, I. Desguerre +20 more
2012Proceedings of the National Academy of Sciences of the United States of America54 citations Open access
Semantic Scholar
Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean fever.
L. Belmahi, A. Sefiani, Corinne Fouveau, J. Feingold +3 more
2006Comptes rendus. Biologies52 citations Open access
Semantic Scholar
The incidence of Rett syndrome in France.
T. Bienvenu, C. Philippe, N. de Roux, M. Raynaud +9 more
2006Pediatric Neurology52 citations
Semantic Scholar
Identification et prise en charge du syndrome HNPCC (hereditary non polyposis colon cancer). prédisposition héréditaire aux cancers du côlon, du rectum et de l'utérus
S. Olschwang, C. Bonaïti-pellié, J. Feingold, T. Frebourg +8 more
200649 citations
Semantic Scholar
Genetic epidemiology of host predisposition microfilaraemia in human loiasis
A. García, L. Abel, M. Cot, P. Richard +5 more
1999Tropical medicine & international health48 citations Open access
Semantic Scholar
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis
H. Corvol, P. Boelle, J. Brouard, N. Knauer +11 more
2008Pediatric Pulmonology47 citations
Semantic Scholar
Revisiting metatropic dysplasia: Presentation of a series of 19 novel patients and review of the literature
D. Geneviève, M. Le Merrer, J. Feingold, A. Munnich +2 more
2008American Journal of Medical Genetics. Part A40 citations
Semantic Scholar
Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis
H. Corvol, N. Nathan, C. Charlier, K. Chadelat +7 more
2007Respiratory Research40 citations Open access
Semantic Scholar
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management].
T. Frébourg, A. Abel, C. BonaÎti-Pellié, L. Brugières +24 more
2001Bulletin du Cancer38 citations
Semantic Scholar
Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.
N. Gigarel, L. Hesters, David C. Samuels, S. Monnot +11 more
2011American Journal of Human Genetics37 citations Open access
Semantic Scholar
Intrafamilial phenotypic variability of osteopetrosis due to chloride channel 7 (CLCN7) mutations
A. Campos‐Xavier, J. Casanova, Y. Doumaz, J. Feingold +2 more
2005American Journal of Medical Genetics. Part A35 citations
Semantic Scholar
Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case
P. Charron, D. Heron, M. Gargiulo, J. Feingold +3 more
2004Prenatal Diagnosis32 citations
Semantic Scholar
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia
N. Canki‐Klain, A. Milić, B. Kovač, Anuška Trlaja +9 more
2004American Journal of Medical Genetics. Part A32 citations
Semantic Scholar
Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients
D. Lorenz, S. Klebe, G. Stevanin, Sandra Thier +9 more
2009European Journal of Human Genetics31 citations Open access
Semantic Scholar
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].
S. Olschwang, C. Bonaiti, J. Feingold, T. Frebourg +8 more
2004Bulletin du Cancer29 citations
Semantic Scholar
DECREASED MORBIDITY IN HOMOZYGOUS SICKLE CELL DISEASE DETECTED AT BIRTH
J. Bardakdjian-Michau, M. Guilloud‐Bataille, M. Maier-Redelsperger, J. Elion +4 more
2002Hemoglobin29 citations
Semantic Scholar
Genetic comparisons of patients with cystic fibrosis with or without meconium ileus. Clinical Centers of the French CF Registry.
J. Feingold, M. Guilloud‐Bataille
1999Annales de Genetique29 citations
Semantic Scholar
Sickle-Cell Disease in Brazzaville, Congo: Genetical, Hematological, Biochemical and Clinical Aspects
R. Mouélé, V. Boukila, V. Fourcade, J. Feingold +1 more
1999Acta Haematologica29 citations
Semantic Scholar
Epidemiologic study of the genetics and environment of asthma, bronchial hyperresponsiveness, and atopy.
F. Kauffmann, M. Dizier, M. Oryszczyn, N. Le Moual +14 more
2002Chest24 citations
Semantic Scholar
Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP‐B) deficiency
M. Tredano, D. N. Cooper, M. Stuhrmann, J. Christodoulou +8 more
2006American Journal of Medical Genetics. Part A23 citations
Semantic Scholar
Analysis of ten candidate genes in autism by association and linkage.
A. Philippe, M. Guilloud-Bataille, M. Martinez, C. Gillberg +9 more
2002American journal of medical genetics23 citations
Semantic Scholar
Parental age in retinoblastoma
C. Pellié, M. Briard, J. Feingold, J. Frézal
2004Humangenetik16 citations
Semantic Scholar
The PSP‐associated MAPT H1 subhaplotype in Guadeloupean atypical Parkinsonism
A. Camuzat, M. Romana, A. Dürr, J. Feingold +3 more
2008Movement Disorders15 citations
Semantic Scholar
Genotype‐Phenotype Relationships
S. Lyonnet, J. Feingold, J. Frézal
200615 citations
Semantic Scholar
Evaluation of biobank constitution and use: multicentre analysis in France and propositions for formalising the activities of research ethics committees.
S. de Montgolfier, G. Moutel, N. Duchange, I. Callies +4 more
2006European Journal of Medical Genetics15 citations Open access
Semantic Scholar

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