Concepedia

John MacMillan

JM

Statistics

Publications

21

Citations

2.6K

H-Index

19

Active since

1992

Affiliations

Royal Children's Hospital(Current)

Royal Brisbane and Women's Hospital

Griffith University

The University of Queensland

University of Wales

John MacMillan is an author at Royal Children's Hospital specializing in life sciences, genetics, and human genetics.

Publications per year

1992–2017

21

Publications

21

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Russell G. Snell, John MacMillan, Jeremy P. Cheadle et al. · Nature Genetics · 1993 · 719 citations

, , +14

PAK3 mutation in nonsyndromic X-linked mental retardation

Kristina M. Allen, Joseph G. Gleeson, Shubha Bagrodia et al. · Nature Genetics · 1998 · 470 citations

, , +13

Phenotypic Characterization of Individuals with 30–40 CAG Repeats in the Huntington Disease (HD) Gene Reveals HD Cases with 36 Repeats and Apparently Normal Elderly Individuals with 36–39 Repeats

David C. Rubinsztein, Jayne Leggo, Rhian Coles et al. · HAL (Le Centre pour la Communication Scientifique Directe) · 1996 · 468 citations

, , +10

Clinical and genetic study of Friedreich ataxia in an Australian population

Martin B. Delatycki, Damien B.B.P. Paris, R. J McKinlay Gardner et al. · American Journal of Medical Genetics · 1999 · 143 citations

, , +13

The methylenetetrahydofolate reductase gene variant C677T influences susceptibility to migraine with aura

Micky Ovcaric, James Sundholm, John MacMillan et al. · Griffith Research Online (Griffith University, Queensland, Australia) · 2004 · 136 citations · Full text

, , +16

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