M. Gross

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Maternal Diets Trigger Sex-Specific Divergent Trajectories of Gene Expression and Epigenetic Systems in Mouse Placenta

A. Gabory, Laure Ferry, I. Fajardy, 2012, PloS one.

Molecular cloning and chromosomal localization of a novel human tracheo-bronchial mucin cDNA containing tandemly repeated sequences of 48 base pairs.

M. Gross, A. Bernheim, V. Guyonnet-Dupérat, 1991, Biochemical and biophysical research communications.

MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.

M. Gross, D. Milewicz, D. Guo, 2014, American journal of human genetics.

An oligonucleotide microarray for mouse imprinted genes profiling

A. Vigé, C. Gallou-Kabani, M. Gross, 2006, Cytogenetic and Genome Research.

Assignment to chromosome 12 of the gene coding for the human cell surface antigen CD9(p24) using the monoclonal antibody ALB6.

M. Gross, D. Weil, J. Frézal, 1985, Annales de genetique.

Human genes for glutathione S-transferases

M. Gross, J. Frézal, N. Cong, 2004, Human Genetics.

[Nutritionnal epigenomics: consequences of unbalanced diets on epigenetics processes of programming during lifespan and between generations].

A. Vigé, C. Gallou-Kabani, M. Gross, 2005, Annales d'endocrinologie.

Localization of the active gene of aldolase on chromosome 16, and two aldolase A pseudogenes on chromosomes 3 and 10

M. Gross, J. Frézal, A. Kahn, 1988, Human Genetics.

The human homologues of Fim1, Fim2/c-Fms, and Fim3, three retroviral integration regions involved in mouse myeloblastic leukemias, are respectively located on chromosomes 6p23, 5q33, and 3q27

M. Gross, J. Frézal, B. Sola, 1989, Human Genetics.

Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization.

M. Gross, C. Junien, D. Weil, 1982, American journal of human genetics.

Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome

M. Gross, G. Jondeau, C. Boileau, 2019, Genes.

Localization of the human oncogene SPI1 on chromosome 11, region p11.22

M. Gross, F. Moreau-Gachelin, J. Frézal, 1990, Human Genetics.

Assignment of human platelet GP2B (GPIIb) gene to chromosome 17, region q21.1-q21.3

M. Gross, J. Frézal, C. Boucheix, 1988, Human Genetics.

Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13

M. Gross, J. Frézal, T. Meo, 1988, Human Genetics.

Assignment of the human CD9 gene to chromosome 12 (region P13) by use of human specific DNA probes

M. Gross, J. Frézal, C. Boucheix, 2004, Human Genetics.

Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells

M. Gross, C. Boileau, F. Chaubet, 2019, Molecular therapy. Nucleic acids.

Assignment of human tracheobronchial mucin gene(s) to 11p15 and a tracheobronchial mucin-related sequence to chromosome 13

M. Gross, J. Frézal, N. Porchet, 1990, Human Genetics.

Human type I procollagen genes are located on different chromosomes.

M. Gross, C. Junien, A. de la Chapelle, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Assignment of the human coproporphyrinogen oxidase to chromosome 9

M. Gross, D. Weil, H. Verneuil, 2004, Human Genetics.

Épigénomique nutritionnelle du syndrome métabolique

A. Vigé, C. Gallou-Kabani, M. Gross, 2005 .

Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16

M. Gross, D. Weil, J. Frézal, 2004, Human Genetics.

Assignment of the ǵene for F‐type phosphofructokinase to human chromosome 10 by somatic cell hybridization and specific immunoprecipitation

M. Gross, D. Weil, A. Kahn, 1980, Annals of human genetics.

Sex- and Diet-Specific Changes of Imprinted Gene Expression and DNA Methylation in Mouse Placenta under a High-Fat Diet

A. Gabory, A. Vigé, S. Mayeur, 2010, PloS one.

2 Implications for Obesity and Common Diseases

A. Vigé, C. Gallou-Kabani, M. Gross, 2007 .

C57BL/6J and A/J Mice Fed a High‐Fat Diet Delineate Components of Metabolic Syndrome

A. Vigé, C. Gallou-Kabani, M. Gross, 2007, Obesity.

Three novel germline mutations in exons 8 and 18 of the retinoblastoma gene.

M. Gross, V. Blanquet, F. Doz, 1994, Human molecular genetics.

The human placental protein 14 (PP14) gene is localized on chromosome 9q34

M. Gross, E. Milgrom, A. Bernheim, 1991, Human Genetics.

Mucin 4 (MUC4) gene: regional assignment (3q29) and RFLP analysis.

M. Gross, A. Bernheim, N. Porchet, 1992, Annales de genetique.

Molecular Basis of Epigenetic Memory

A. Vigé, C. Gallou-Kabani, M. Gross, 2007 .

Nutri-epigenomics: lifelong remodelling of our epigenomes by nutritional and metabolic factors and beyond

A. Vigé, C. Gallou-Kabani, M. Gross, 2007, Clinical chemistry and laboratory medicine.

[Nutritional epigenomics of metabolic syndrome].

A. Vigé, C. Gallou-Kabani, M. Gross, 2005, Medecine sciences : M/S.

TGFB2 loss of function mutations cause familial thoracic aortic aneurysms and acute aortic dissections associated with mild systemic features of the Marfan syndrome

Jay Shendure, Mathilde Varret, Catherine Boileau, 2012, Nature Genetics.

Dietary Alleviation of Maternal Obesity and Diabetes: Increased Resistance to Diet-Induced Obesity Transcriptional and Epigenetic Signatures

Claudine Junien, Jean-Philippe Jais, A. Gabory, 2013, PloS one.

The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele.

M. Gross, G. Jondeau, L. Gouya, 2015, Human molecular genetics.

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

T. Bourgeron, E. Génin, M. Gross, 2018, European Journal of Human Genetics.

Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression

M. Gross, G. Jondeau, C. Boileau, 2018, Genes.

Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassay

M. Gross, D. Weil, B. Grandchamp, 2004, Human Genetics.

Assignment of the human gene for δ aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassay

M. Gross, V. C. N'guyen, D. Weil, 1984, Annals of human genetics.

Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability

M. Gross, G. Jondeau, L. Gouya, 2020, Genes.

Resistance to high-fat diet in the female progeny of obese mice fed a control diet during the periconceptual, gestation, and lactation periods.

A. Vigé, C. Gallou-Kabani, M. Gross, 2007, American journal of physiology. Endocrinology and metabolism.

ABCC8 (SUR1) and KCNJ11 (KIR6.2) Mutations in Persistent Hyperinsulinemic Hypoglycemia of Infancy and Evaluation of Different Therapeutic Measures

M. Gross, C. Junien, F. Baş, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm

M. Gross, K. Sekiguchi, D. Milewicz, 2020, Genetics in Medicine.

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm

M. Gross, K. Sekiguchi, D. Milewicz, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Panel of twenty-five independent man-rodent hybrids for human genetic marker mapping.

M. Gross, D. Weil, J. Frézal, 1986, Annales de genetique.

Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qter

M. Gross, J. Frézal, M. Buckingham, 2004, Human Genetics.

Regional mapping of the human renin gene to 1q32 by in situ hybridization.

M. Gross, J. Frézal, F. Soubrier, 1989, Annales de Genetique.

Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing.

M. Gross, V. Blanquet, M. Goossens, 1993, Human Molecular Genetics.

The human ASM (adult skeletal muscle) gene: expression and chromosomal assignment to 11p15.

M. Gross, M. Leibovitch, B. Solhonne, 1991, Biochemical and biophysical research communications.

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

T. Bourgeron, E. Génin, M. Gross, 2018, European Journal of Human Genetics.