Peter Rogan
Peter Rogan
Prof. Biochemistry, Oncology & Epi/Biostatistics at University of Western Ontario
Verified email at uwo.ca - Homepage
TitleCited byYear
Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression
V Lamba, J Lamba, K Yasuda, S Strom, J Davila, ML Hancock, ...
Journal of Pharmacology and Experimental Therapeutics 307 (3), 906-922, 2003
3932003
Imprinting-mutation mechanisms in Prader-Willi syndrome
T Ohta, TA Gray, PK Rogan, K Buiting, JM Gabriel, S Saitoh, B Muralidhar, ...
The American Journal of Human Genetics 64 (2), 397-413, 1999
2941999
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
JM Amos-Landgraf, Y Ji, W Gottlieb, T Depinet, AE Wandstrat, SB Cassidy, ...
The American Journal of Human Genetics 65 (2), 370-386, 1999
2721999
The frequency of uniparental disomy in Prader-Willi syndrome: implications for molecular diagnosis
MJ Mascari, W Gottlieb, PK Rogan, MG Butler, DA Waller, JAL Armour, ...
New England Journal of Medicine 326 (24), 1599-1607, 1992
2641992
Information analysis of human splice site mutations
PK Rogan, BM Faux, TD Schneider
Human mutation 12 (3), 153-171, 1998
2011998
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations
S Saitoh, K Buiting, PK Rogan, JL Buxton, DJ Driscoll, J Arnemann, ...
Proceedings of the National Academy of Sciences 93 (15), 7811-7815, 1996
1901996
Automated splicing mutation analysis by information theory
VK Nalla, PK Rogan
Human mutation 25 (4), 334-342, 2005
1762005
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the bA3/A1-crystallin gene
C Kannabiran, PK Rogan, L Olmos, S Basti, GN Rao, M Kaiser-Kupfer, ...
Mol Vis 4, 21, 1998
1441998
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns
Z Michael, R Jacobs, Patricia, James, P Rogan, S Sherman, T Hassold
Human Genetics 94, 411-417, 1994
1361994
Mutations that alter RNA splicing of the human HPRT gene: a review of the spectrum
JP O'Neill, PK Rogan, N Cariello, JA Nicklas
Mutation Research/Reviews in Mutation Research 411 (3), 179-214, 1998
1231998
Method for rapid identification of prokaryotic and eukaryotic organisms
PK Rogan
US Patent 5,849,492, 1998
1201998
Clinical spectrum and molecular diagnosis of Angelman and Prader‐Willi syndrome patients with an imprinting mutation
S Saitoh, K Buiting, SB Cassidy, JM Conroy, DJ Driscoll, JM Gabriel, ...
American journal of medical genetics 68 (2), 195-206, 1997
1141997
Human SP-A locus: allele frequencies and linkage disequilibrium between the two surfactant protein A genes.
J Floros, S DiAngelo, M Koptides, AM Karinch, PK Rogan, H Nielsen, ...
American journal of respiratory cell and molecular biology 15 (4), 489-498, 1996
851996
Study of nucleic acids isolated from ancient remains
PK Rogan, JJ Salvo
American Journal of Physical Anthropology 33 (S11), 195-214, 1990
791990
Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans
A Gaedigk, A Bhathena, L Ndjountche, RE Pearce, SM Abdel-Rahman, ...
The pharmacogenomics journal 5 (3 (PMID 15768052)), 173, 2005
782005
Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans.
A Gaedigk, A Bhathena, L Ndjountché, RE Pearce, SM Abdel-Rahman, ...
Pharmacogenomics J. 5 (4), 276, 2005
782005
Information theory-based analysis of CYP2C19, CYP2D6 and CYP3A5 splicing mutations
PK Rogan, S Svojanovsky, JS Leeder
Pharmacogenetics and Genomics 13 (4), 207-218, 2003
762003
Organization of the ABCR gene: analysis of promoter and splice junction sequences.
R Allikmets, WW Wasserman, A Hutchinson, P Smallwood, J Nathans, ...
Gene 215 (1), 111-122, 1998
761998
A new missense mutation, Arg719Gln, in the?-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy
MW Consevage, GC Salada, BG Baylen, RL Ladda, PK Rogan
Human Molecular Genetics 3 (9), 1716-1716, 1994
641994
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
P Peterlongo, I Catucci, M Colombo, L Caleca, E Mucaki, M Bogliolo, ...
Human molecular genetics 24 (18), 5345-5355, 2015
622015
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