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J. Lagarde · SciRah

Researcher profile · Semantic Scholar

J. Lagarde

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J. Lagarde — researcher profile on SciRah

h-index: 12
Works: 29
Citations: 1,046

Most-cited papers

The γ e4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration
Eric H. Souied, P. Benlian, P. Amouyel, J. Feingold +5 more
1998285 citations
Semantic Scholar
A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.
F. Jeanneteau, B. Funalot, J. Jankovic, H. Deng +3 more
2006Proceedings of the National Academy of Sciences of the United States of America194 citations Open access
Semantic Scholar
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration.
E. Souied, P. Benlian, P. Amouyel, J. Feingold +5 more
1998American journal of ophthalmology-glaucoma144 citations
Semantic Scholar
High frequency of the apolipoprotein E *4 allele in African pygmies and most of the African populations in sub-Saharan Africa.
L. Zekraoui, J. Lagarde, A. Raisonnier, N. Gérard +2 more
1997Human Biology: The Official Publication of the American Association of Anthropological Genetics78 citations
Semantic Scholar
The genes for gonadotropin‐releasing hormone and its receptor are expressed in human breast with fibrocystic disease and cancer
M. Kottler, A. Starzec, M. Carré, J. Lagarde +2 more
1997International Journal of Cancer72 citations Open access
Semantic Scholar
Functional interaction between -629C/A, -971G/A and -1337C/T polymorphisms in the CETP gene is a major determinant of promoter activity and plasma CETP concentration in the REGRESS Study.
E. Frisdal, A. Klerkx, W. Le Goff, Michael W. T. Tanck +5 more
2005Human Molecular Genetics66 citations
Semantic Scholar
Spontaneous pregnancy in a patient who was homozygous for the Q106R mutation in the gonadotropin-releasing hormone receptor gene.
D. Dewailly, A. Boucher, C. Decanter, J. Lagarde +2 more
2002Fertility and Sterility45 citations Open access
Semantic Scholar
A case of complete hypogonadotropic hypogonadism with a mutation in the gonadotropin-releasing hormone receptor gene.
S. Wołczyński, P. Laudański, K. Jarząbek, H. Mittre +2 more
2003Fertility and Sterility38 citations Open access
Semantic Scholar
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B‐100
P. Benlian, J. de Gennes, François Dairou, B. Hermelin +7 more
1996Human Mutation30 citations Open access
Semantic Scholar
Importance, mechanisms and limitations of the distant bystander effect in cancer gene therapy of experimental liver tumors.
C. Engelmann, J. Heslan, M. Fabre, J. Lagarde +2 more
2002Cancer Letters20 citations
Semantic Scholar
The GnRH receptor gene is preferentially expressed in functioning gonadotroph adenomas and displays a Mae III polymorphism site
M. Kottler, D. Seret-Bégué, N. Lahlou, M. Assayag +8 more
1998Clinical Endocrinology20 citations
Semantic Scholar
Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients.
G. Lucotte, A. Houzet, C. Hubans, J. Lagarde +1 more
2009Genetic Counseling15 citations
Semantic Scholar
Assessment of French patients with LPL deficiency for French Canadian mutations.
L. Foubert, J. de Gennes, J. Lagarde, E. Ehrenborg +4 more
1997Journal of Medical Genetics12 citations Open access
Semantic Scholar
Does electrophoresis reliably screen for high serum lipoprotein Lp(a)?
É. Bruckert, J. Truffert, J. de Gennes, J. Lagarde +4 more
1990Clinica chimica acta; international journal of clinical chemistry9 citations
Semantic Scholar
Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele.
Laila O. Abdel-Wareth, S. Pimstone, J. Lagarde, A. Raisonnier +4 more
1997Atherosclerosis8 citations
Semantic Scholar
Mutations of the noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP).
G. Lucotte, J. Lagarde
2007Genetic Counseling4 citations
Semantic Scholar
An analysis of mutations underlying lipoprotein lipase (LPL) deficiency in France
L. Foubert, É. Gagné, J. de Gennes, Yuanhong Ma +7 more
19943 citations
Semantic Scholar
[Genotyping of apolipoprotein E (alleles epsilon 2, epsilon 3 and epsilon 4) from capillary blood].
J. Lagarde, P. Benlian, L. Zekraoui, A. Raisonnier
1995Annales de Biologie Clinique2 citations
Semantic Scholar
Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa.
Eric H. Souied, P. Benlian, J. Rozet, S. Gerber +6 more
1998Vision Research1 citations Open access
Semantic Scholar
A new informative Alw 26 I polymorphism in exon 10 of the human low density lipoprotein receptor gene. Application to prenatal diagnosis
M. Kottler, J. Lagarde, K. Dahan, L. Zekraoui +1 more
1998Human Mutation1 citations Open access
Semantic Scholar
Compound heterozygotes for familial defective apo B-100 (FDB) and familial hypercholesterolemia (FH)
P. Benlian, J. de Gennes, F. Dairou, B. Hermelin +5 more
19941 citations
Semantic Scholar
Rapid communication Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa
E. Souied, P. Benlian, J. Rozet, S. Gerber +5 more
19980 citations
Semantic Scholar
Assessment ofFrench patients withLPL deficiency forFrench Canadian mutations
J. Lagarde, J. Girardet, M. Hayden, P. Benlian
19970 citations
Semantic Scholar
Processing of an asynchronous signal including a periodic synchronization pulse train
P. Leurent, J. Lagarde
19960 citations
Semantic Scholar
Circuit for restoring bit transmitted with asynchronous signal, method for detecting synchronous burst, method for controlling bit restoration error, and method for detecting signal with high frequency loss
J. Lagarde, P. Leurent, ジャン−ピエール・ラガルド, パトリス・リュレン
19960 citations
Semantic Scholar
Founder effect for familial defective apo B-100 (FDB) mutation in France
I. Ginon, J. de Gennes, A. Raisonnier, J. Lagarde +6 more
19940 citations
Semantic Scholar
Investigation of French Canadian founder mutations for lipoprotein lipase deficiency (LPL) in France
L. Foubert, J. de Gennes, É. Gagné, Yuanhong Ma +5 more
19940 citations
Semantic Scholar
Familial defective apo B-100 (FDB) in France: frequency and clinical presentation in families
I. Ginon, J. de Gennes, F. Dairou, J. Lecerf +7 more
19940 citations
Semantic Scholar
[Pseudo-hypertriglyceridemia caused by glycerol kinase deficiency].
M. L. Sanson-Raffin, G. Turpin, T. Tzotzas, J. Lagarde +3 more
1989La Revue de medecine interne0 citations
Semantic Scholar

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