(Q57312415)

David-Alexandre Trégouët

11

0 references

Nicolas Levy

Nicolas Levy

8

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Frédéric Fumeron

Frederic Fumeron

4

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Michel Marre

Michel Marre

5

0 references

Marie-Christine Alessi

Marie-Christine Alessi

2

1 reference

ORCID Public Data File 2021

author name string

Benedicte Fontaine-Bisson

1

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Noemie Saut

3

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Anne Dutour

6

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Catherine Badens

7

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Jean Tichet

9

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Irene Juhan-Vague

10

0 references

Beverly Balkau

12

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Pierre-Emmanuel Morange

Journal of Molecular Medicine

13

0 references

publication date

16 October 2009

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published in

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volume

88

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issue

2

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page(s)

193-201

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exact match

https://scigraph.springernature.com/pub.10.1007/s00109-009-0548-y

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cites work

Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.

1 reference

12 December 2020

Proposed criteria for the diagnosis of diabetes: evidence from a French epidemiological study (D.E.S.I.R.).

1 reference

12 December 2020

Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids

1 reference

12 December 2020

Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in a general population: Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR).

1 reference

12 December 2020

Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes

1 reference

12 December 2020

A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies.

1 reference

12 December 2020

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

1 reference

12 December 2020

Genetic epidemiology and haplotypes

1 reference

12 December 2020

Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects

1 reference

12 December 2020

Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromes

1 reference

12 December 2020

SREBP in signal transduction: cholesterol metabolism and beyond

1 reference

12 December 2020

Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians

1 reference

12 December 2020

Human laminopathies: nuclei gone genetically awry

1 reference

12 December 2020

Premature aging in mice activates a systemic metabolic response involving autophagy induction.

1 reference

12 December 2020

Prelamin A, Zmpste24, misshapen cell nuclei, and progeria--new evidence suggesting that protein farnesylation could be important for disease pathogenesis

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

1 reference

12 December 2020

Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies

1 reference

12 December 2020

Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement

1 reference

12 December 2020

Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whites

1 reference

12 December 2020

Automated detection of informative combined effects in genetic association studies of complex traits.

1 reference

12 December 2020

Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach.

1 reference

12 December 2020

Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study

1 reference

12 December 2020

Common genomic variation in LMNA modulates indexes of obesity in Inuit

1 reference

12 December 2020

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy

1 reference

12 December 2020

An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese

1 reference

12 December 2020

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

1 reference

12 December 2020

Analysis of the lamin A/C gene as a candidate for type II diabetes susceptibility in Pima Indians

1 reference

12 December 2020

A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

1 reference

12 December 2020

A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm.

1 reference

12 December 2020

Isoprenylcysteine carboxyl methyltransferase deficiency in mice

1 reference

12 December 2020

Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities

1 reference

12 December 2020

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

1 reference

12 December 2020

Variation in the lamin A/C gene: associations with metabolic syndrome

1 reference

12 December 2020