Dennis Bulman
Dennis Bulman
Unknown affiliation
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Cited by
Cited by
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, K Abdelmohsen, A Abe, MJ Abedin, H Abeliovich, ...
Autophagy 12 (1), 1-222, 2016
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
RA Ophoff, GM Terwindt, MN Vergouwe, R Van Eijk, PJ Oefner, ...
Cell 87 (3), 543-552, 1996
A full genome search in multiple sclerosis
GC Ebers, K Kukay, DE Bulman, AD Sadovnick, G Rice, C Anderson, ...
Nature genetics 13 (4), 472-476, 1996
A population-based study of multiple sclerosis in twins
GC Ebers, DE Bulman, AD Sadovnick, DW Paty, S Warren, W Hader, ...
New England Journal of Medicine 315 (26), 1638-1642, 1986
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle
EE Zubrzycka-Gaarn, DE Bulman, G Karpati, AHM Burghes, B Belfall, ...
Nature 333 (6172), 466-469, 1988
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
SB England, LVB Nicholson, MA Johnson, SM Forrest, DR Love, ...
Nature 343 (6254), 180-182, 1990
Rare-disease genetics in the era of next-generation sequencing: discovery to translation
KM Boycott, MR Vanstone, DE Bulman, AE MacKenzie
Nature Reviews Genetics 14 (10), 681-691, 2013
A population‐based study of multiple sclerosis in twins: update
AD Sadovnick, H Armstrong, GPA Rice, D Bulman, L Hashimoto, ...
Annals of neurology 33 (3), 281-285, 1993
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
JB Rivière, GM Mirzaa, BJ O'Roak, M Beddaoui, D Alcantara, RL Conway, ...
Nature genetics 44 (8), 934, 2012
A novel sodium channel mutation in a family with hypokalemic periodic paralysis
DE Bulman, KA Scoggan, MD Van Oene, MW Nicolle, AF Hahn, LL Tollar, ...
Neurology 53 (9), 1932-1932, 1999
Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
SL Sawyer, T Hartley, DA Dyment, CL Beaulieu, J Schwartzentruber, ...
Clinical genetics 89 (3), 275-284, 2016
Parkinson’s disease-linked LRRK2 is expressed in circulating and tissue immune cells and upregulated following recognition of microbial structures
M Hakimi, T Selvanantham, E Swinton, RF Padmore, Y Tong, G Kabbach, ...
Journal of neural transmission 118 (5), 795-808, 2011
Mutations in EZH2 cause Weaver syndrome
WT Gibson, RL Hood, SH Zhan, DE Bulman, AP Fejes, R Moore, ...
The American Journal of Human Genetics 90 (1), 110-118, 2012
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project
CL Beaulieu, J Majewski, J Schwartzentruber, ME Samuels, ...
The American Journal of Human Genetics 94 (6), 809-817, 2014
Dystrophin expression in the human retina is required for normal function as defined by electroretinography
DAM Pillers, DE Bulman, RG Weleber, DA Sigesmund, MA Musarella, ...
Nature genetics 4 (1), 82-86, 1993
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone
L Huang, K Szymanska, VL Jensen, AR Janecke, AM Innes, EE Davis, ...
The American Journal of Human Genetics 89 (6), 713-730, 2011
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers.
CJ Klein, DD Coovert, DE Bulman, PN Ray, JR Mendell, AH Burghes
American journal of human genetics 50 (5), 950, 1992
Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease
G Shi, JR Lee, DA Grimes, L Racacho, D Ye, H Yang, OA Ross, M Farrer, ...
Human molecular genetics 20 (10), 1966-1974, 2011
A novel locus for inherited myoclonus-dystonia on 18p11
DA Grimes, F Han, AE Lang, PS George-Hyssop, L Racacho, DE Bulman
Neurology 59 (8), 1183-1186, 2002
Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly
MA Lines, L Huang, J Schwartzentruber, SL Douglas, DC Lynch, ...
The American Journal of Human Genetics 90 (2), 369-377, 2012
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