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 · 494 citations

Hematological Malignancy, Genetic Disorder, Mixed-phenotype Acute Leukemia +8

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 · 246 citations · Full text

Neurological Disorder, Corticobasal Degeneration, Brain Iron Accumulation +19

Diagnostic criteria for facioscapulohumeral muscular dystrophy

G.W. Padberg, Peter Lunt, Manuela C. Koch et al. · Neuromuscular Disorders · 1991 · 218 citations

Diagnosis, Motor Disorder, Medicine +3

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 · 208 citations

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 · 136 citations · Full text