Marc Jeanpierre

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Steven L. Roberds, France Leturcq, Valérie Allamand et al. · Cell · 1994 · 456 citations

Rare Diseases, Missense Mutations, Developmental Biology +9

A rapid method for the purification of DNA from blood

Marc Jeanpierre · Nucleic Acids Research · 1987 · 320 citations

Dna, Engineering, Genetics +22

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

Marc Jeanpierre, C Turleau, Alain Aurias et al. · Human Molecular Genetics · 1993 · 283 citations

Embryonic-like Methylation Pattern, Icf Dna, Epigenetic Change +19

<i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans

Jacques Young, Jérôme Bouligand, Bruno Francou et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 245 citations · Full text

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre et al. · Nature Genetics · 1995 · 190 citations

Rare Diseases, Variable Severity, Ophthalmology +6