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M. Kœnig | Researchclopedia

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M. Kœnig

Centre National de la Recherche Scientifique ORCID

678

Works

24,408

Citations

65

h-index

272

i10-index

Research Topics

Laser-Plasma Interactions and Diagnostics Laser-induced spectroscopy and plasma High-pressure geophysics and materials

Affiliations

Tokyo Institute of Technology2009–2009

University of Miyazaki2009–2009

Queen's University Belfast2006–2006

University of Dayton1987–1988

Lawrence Livermore National Laboratory2003–2013

Top Works

Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

Victoria Campuzano,Laura Montermini,et al.

19962,758 citations

Atomic and Molecular Physics

Laser-Matter Interactions and Applications

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

M. Kœnig,Eric P. Hoffman,et al.

19872,391 citations

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

M. Kœnig,Anthony P. Monaco,et al.

19881,516 citations

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

M. Kœnig,Alan H. Beggs,et al.

1989961 citations

Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes

Victoria Campuzano,Laura Montermini,et al.

1997735 citations

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

Alan H. Beggs,M. Kœnig,et al.

1990695 citations

Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

Karim Ouahchi,Makoto Arita,et al.

1995567 citations

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

Hana Koutníková,Victoria Campuzano,et al.

1997473 citations

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

Pascale Bomont,L Cavalier,et al.

2000412 citations