Concepedia

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Monika Hartig, Arcangela Iuso, Tobias B. Haack, Tomasz Kmieć, Elżbieta Jurkiewicz, Katharina Heim, Sigrun Roeber, Victoria Tarabin, Sabrina Dusi, Małgorzata Krajewska‐Walasek,

The American Journal of Human Genetics · 2011 · 266 citations · 15 references

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15

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.

Andrew Hughes, S. E. Daniel, Linda Kilford et al. · Journal of Neurology Neurosurgery & Psychiatry · 1992 · 10.4K citations · Full text

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Merlin—rapid analysis of dense genetic maps using sparse gene flow trees

Gonçalo R. Abecasis, Stacey S. Cherny, William Cookson et al. · Nature Genetics · 2001 · 3.4K citations

, , +15

Human non-synonymous SNPs: server and survey

Vasily Ramensky · Nucleic Acids Research · 2002 · 2.3K citations · Full text

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Newton—Raphson and EM Algorithms for Linear Mixed-Effects Models for Repeated-Measures Data

Mary J. Lindstrom, Douglas M. Bates · Journal of the American Statistical Association · 1988 · 879 citations

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A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

Bing Bing Zhou, Shawn K. Westaway, Barbara Levinson et al. · Nature Genetics · 2001 · 761 citations

, , +6