Peter Lunt

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

Pia Østergaard, Michael A. Simpson, Fiona Connell et al. · Nature Genetics · 2011 · 503 citations

Life Sciences, Genetics, Molecular Genetics +10

Beta-propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation

Susan J. Hayflick, Michael C. Kruer, Allison Gregory et al. · Brain · 2013 · 249 citations · Full text

Life Sciences, Genetics, Neurology +17

Diagnostic criteria for facioscapulohumeral muscular dystrophy

G.W. Padberg, Peter Lunt, Manuela C. Koch et al. · Neuromuscular Disorders · 1991 · 220 citations

Medicine, Pathobiology, Neuromuscular Disorders +7

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

Peter Lunt, Philip Jardine, Manuela C. Koch et al. · Human Molecular Genetics · 1995 · 209 citations

Medicine, Genetics, Molecular Genetics +11

The Opitz syndrome gene product, MID1, associates with microtubules

Susann Schweiger, John Foerster, Tanja Lehmann et al. · Proceedings of the National Academy of Sciences · 1999 · 137 citations

Life Sciences, Genetics, Molecular Biology +14