Peter Pearson
Peter Pearson
Visiting Professor Human Genetics, Dept Genetics and Evolutionary Biology, University of Sao Paulo
Verified email at ib.usp.br
Title
Cited by
Cited by
Year
The variability of female reproductive ageing
ER Te Velde, PL Pearson
Human reproduction update 8 (2), 141-154, 2002
12242002
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
ST Reeders, MH Breuning, KE Davies, RD Nicholls, AP Jarman, ...
Nature 317 (6037), 542-544, 1985
8591985
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
JT Den Dunnen, PM Grootscholten, E Bakker, LA Blonden, HB Ginjaar, ...
American journal of human genetics 45 (6), 835, 1989
6371989
Technique for identifying Y chromosomes in human interphase nuclei
PL Pearson, M Bobrow, CG Vosa
Nature 226 (5240), 78-80, 1970
5721970
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome
U Francke, HD Ochs, B de Martinville, J Giacalone, V Lindgren, ...
American journal of human genetics 37 (2), 250, 1985
5181985
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization …
T Cremer, J Landegent, A Brückner, HP Scholl, M Schardin, HD Hager, ...
Human genetics 74 (4), 346-352, 1986
4971986
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
KE Davies, PL Pearson, PS Harper, JM Murray, T O'Brien, M Sarfarazi, ...
Nucleic Acids Research 11 (8), 2303-2312, 1983
4671983
Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic mice
BT Lamb, SS Sisodia, AM Lawler, HH Slunt, CA Kitt, WG Kearns, ...
Nature genetics 5 (1), 22-30, 1993
3761993
Identification of a new copper metabolism gene by positional cloning in a purebred dog population
B van de Sluis, J Rothuizen, PL Pearson, BA van Oost, C Wijmenga
Human molecular genetics 11 (2), 165-173, 2002
3722002
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q
SC Bakker, EM Van Der Meulen, JK Buitelaar, LA Sandkuijl, DL Pauls, ...
The American Journal of Human Genetics 72 (5), 1251-1260, 2003
3362003
The role of genetic factors in age at natural menopause
JP De Bruin, H Bovenhuis, PAH Van Noord, PL Pearson, ...
Human Reproduction 16 (9), 2014-2018, 2001
3262001
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1. 28
SS Bhattacharya, AF Wright, JF Clayton, WH Price, CI Phillips, ...
Nature 309 (5965), 253-255, 1984
3201984
Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9
M Bobrow, K Madan, PL Pearson
Nature New Biology 238 (82), 122-124, 1972
2891972
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes
P Devilee, RF Thierry, T Kievits, R Kolluri, AHN Hopman, HF Willard, ...
Cancer research 48 (20), 5825-5830, 1988
2701988
Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q.
P Devilee, ND Kuipers, J Hermans, PL Pearson, CJ Cornelisse
Oncogene 6 (9), 1705-1711, 1991
2581991
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma
P Devilee, M van den Broek, N Kuipers-Dukshoorn, R Kolluri, PM Khan, ...
Genomics 5 (3), 554-560, 1989
2521989
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs
E Bakker, N Goor, K Wrogemann, LM Kunkel, WA Fenton, ...
The Lancet 325 (8430), 655-658, 1985
2481985
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy
MH Hofker, MC Wapenaar, N Goor, E Bakker, GJB Van Ommen, ...
Human genetics 70 (2), 148-156, 1985
2321985
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643
KK Kidd, AM Bowcock, J Schmidtke, RK Track, F Ricciuti, G Hutchings, ...
Cytogenetic and Genome Research 51 (1-4), 622-643, 1989
2211989
Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels
JT Den Dunnen, E Bakker, EGK Breteler, PL Pearson, GJB Van Ommen
Nature 329 (6140), 640-642, 1987
2211987
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