Michael W. Glynn

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Maria Eriksson, W. Ted Brown, Leslie B. Gordon et al. · Nature · 2003 · 2.2K citations · Full text

Medicine, Genetics, Molecular Genetics +5

Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Jianming Fang, Susan L. Dagenais, Robert P. Erickson et al. · The American Journal of Human Genetics · 2000 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Incomplete processing of mutant lamin A in Hutchinson–Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition

Michael W. Glynn, Thomas W. Glover · Human Molecular Genetics · 2005 · 252 citations

Life Sciences, Genetics, Molecular Biology +14

Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content.

Namadev Baskaran, Rajendra P. Kandpal, A.K. Bhargava et al. · Genome Research · 1996 · 175 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model

Jeffrey W. Innis, Douglas P. Mortlock, Zhi Chen et al. · Human Molecular Genetics · 2004 · 48 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14