Jean‐Marc Lalouel

University of Utah — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

24h-index5.6kcitations36works0.02yr avg
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Research Topics

Genetic Associations and Epidemiology(9), Renin-Angiotensin System Studies(8), Hormonal Regulation and Hypertension(8), Chromosomal and Genetic Variations(6), Genomics and Chromatin Dynamics(4)

Publications36 total

AGT Genetic Variation, Plasma AGT, and Blood Pressure: An Analysis of the Utah Genetic Reference Project Pedigrees
American Journal of Hypertension·2010· 15 cited
Genotype–phenotype analysis of angiotensinogen polymorphisms and essential hypertension: the importance of haplotypes
Journal of Hypertension·2009· 43 citedOpen Access
A human polymorphism affects NEDD4L subcellular targeting by leading to two isoforms that contain or lack a C2 domain
BMC Cell Biology·2009· 20 citedOpen Access
From Genetics to Mechanism of Disease Liability
Advances in genetics·2008· 12 cited
NEDD4L protein truncating variant (v13[G/A]: rs4149601) is associated with essential hypertension in a sample of the Japanese population
Geriatrics and gerontology international/Geriatrics & gerontology international·2007· 8 cited
Hypervolemia of pregnancy is not maintained in mice chronically overexpressing angiotensinogen
American Journal of Obstetrics and Gynecology·2006· 14 cited
Haplotype Association Analysis of AGT Variants with Hypertension-Related Traits: The HyperGEN Study
Human Heredity·2005· 25 cited
Natural Selection and Population History in the Human Angiotensinogen Gene (AGT): 736 Complete AGT Sequences in Chromosomes from Around the World
The American Journal of Human Genetics·2004· 132 citedOpen Access
Elements of a Paracrine Tubular Renin-Angiotensin System Along the Entire Nephron
Hypertension·1999· 292 cited
Haplotypes of Angiotensinogen in Essential Hypertension
The American Journal of Human Genetics·1997· 286 citedOpen Access
Blunted renal vascular response to angiotensin II is associated with a common variant of the angiotensinogen gene and obesity
Journal of Hypertension·1996· 157 cited
The Carboxy‐Terminal Domain of Lipoprotein Lipase Induces Cellular Catabolism of Normal Very Low Density Lipoproteins via the Low Density Lipoprotein Receptor—Related Protein/α<sub>2</sub>‐Macroglobulin Receptor
Annals of the New York Academy of Sciences·1994· 9 cited
An Extended Genetic Linkage Map and an "Index" Map for Human Chromosome 17
Genomics·1993· 24 cited
Molecular basis of human hypertension: Role of angiotensinogen
Cell·1992· 1.9k cited
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase
Nature Genetics·1992· 336 citedOpen Access
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension
Nature Genetics·1992· 381 cited
Linkage analysis in human genetics
1992· 35 cited
Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22
Human Molecular Genetics·1992· 19 cited
A detailed genetic map of the long arm of chromosome 11
Genomics·1990· 101 cited
Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q
Genomics·1990· 133 cited
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Frequent Co-authors

Mark Leppert(13), R. White(10), P. O’Connell(7), Andreas Rohrwasser(6), Xavier Jeunemaı̂tre(5), Lynn B. Jorde(5), Richard P. Lifton(4), Roger R. Williams(4), Yusuke Nakamura(4), Christopher S. Williams(3), Paul N. Hopkins(3), Dora Stauffer(3), Ituro Inoue(3), Mitsuru Emi(3), Mark Lathrop(3), Mark Lathrop(3), Rosemarie Plaetke(3), Anne Charru(2), Steven C. Hunt(2), Pierre Corvol(2)