P. Pearson - Publications, H-index & Citations

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P. Pearson

universidade de sao paulo

63H-index

443Paper Count

1.5WCitation Count

Published Papers 34

Publication Date

Increased DNA Copy Number Variation Mosaicism in Elderly Human Brain

NEURAL PLASTICITY

IF3.7

2018-06-28

OAAI

Villela, Darine; Suemoto, Claudia K.; Leite, Renata; Pasqualucci, Carlos Augusto; Grinberg, Lea T.; Pearson, Peter; Rosenberg, Carla

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Large germline copy number variations as predisposing factor in childhood neoplasms

FUTURE ONCOLOGY

IF2.6

2014-08-22

OAAI

Victorino Krepischi, Ana Cristina; Capelli, Leonardo Pires; Silva, Amanda Goncalves; Souza de Araujo, Erica Sara; Pearson, Peter Lees; Heck, Benjamin; Lima da Costa, Cecilia Maria; de Camargo, Beatriz; Rosenberg, Carla

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The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2014-01-01

OAAI

Silva, Amanda G.; Krepischi, Ana C. V.; Pearson, Peter L.; Hainaut, Pierre; Rosenberg, Carla; Achatz, Maria Isabel

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Germline BAX Deletion in a Patient With Melanoma and Gastrointestinal Stromal Tumor

AMERICAN JOURNAL OF GASTROENTEROLOGY

IF7.6

2013-08-01

OAAI

Silva, Amanda G.; Lisboa, Bianca C. G.; Achatz, Maria Isabel W.; Carraro, Dirce M.; da Cunha, Isabela W.; Pearson, Peter L.; Krepischi, Ana C. V.; Rosenberg, Carla

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Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2013-06-19

OAAI

Silva, Amanda G.; Krepischi, Ana C. V.; Torrezan, Giovana T.; Capelli, Leonardo P.; Carraro, Dirce M.; D'Angelo, Carla S.; Koiffmann, Celia P.; Zatz, Mayana; Naslavsky, Michel S.; Masotti, Cibele; Otto, Paulo A.; Achatz, Maria I. W.; Mills, Ryan E.; Lee, Charles; Pearson, Peter L.; Rosenberg, Carla

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Number of rare germline CNVs and TP53 mutation types

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2012-12-21

OAAI

Silva, Amanda G.; Achatz, Maria Isabel W.; Krepischi, Ana C. V.; Pearson, Peter L.; Rosenberg, Carla

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Germline copy number variations and cancer predisposition

FUTURE ONCOLOGY

IF2.6

2012-04-19

PREAI

Victorino Krepischi, Ana Cristina; Pearson, Peter Lees; Rosenberg, Carla

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Germline DNA copy number variation in familial and early-onset breast cancer

BREAST CANCER RESEARCH

IF5.6

2012-02-07

OAAI

Krepischi, Ana C. V.; Achatz, Maria Isabel W.; Santos, Erika M. M.; Costa, Silvia S.; Lisboa, Bianca C. G.; Brentani, Helena; Santos, Tiago M.; Goncalves, Amanda; Nobrega, Amanda F.; Pearson, Peter L.; Vianna-Morgante, Angela M.; Carraro, Dirce M.; Brentani, Ricardo R.; Rosenberg, Carla

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Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy

EPILEPSIA

IF6.6

2010-09-30

OAAI

Victorino Krepischi, Ana Cristina; Knijnenburg, Jeroen; Bertola, Debora Romeo; Kim, Chong Ae; Pearson, Peter Lees; Bijlsma, Emilia; Szuhai, Karoly; Kok, Fernando; Vianna-Morgante, Angela Maria; Rosenberg, Carla

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A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3

HUMAN GENETICS

IF3.6

2008-05-21

PREAI

Lezirovitz, Karina; Maestrelli, Sylvia Regina Pedrosa; Cotrim, Nelson Henderson; Otto, Paulo A.; Pearson, Peter L.; Mingroni-Netto, Regina Celia

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Role of genetic analyses in cardiology - Part II: Heritability estimation for gene searching in multifactorial diseases

CIRCULATION

IF38.6

2006-02-28

OAAI

van Asselt, KM; Kok, HS; van der Schouw, YT; Peeters, PHM; Pearson, PL; Grobbee, DE

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Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

MOLECULAR PSYCHIATRY

IF10.1

2005-10-04

PREAI

Ogdie, MN; Bakker, SC; Fisher, SE; Francks, C; Yang, MH; Cantor, RM; Loo, SK; van der Meulen, E; Pearson, P; Buitelaar, J; Monaco, A; Nelson, SF; Sinke, RJ; Smalley, SL

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Accurate determination of microsatellite allele frequencies in pooled DNA samples

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2004-08-11

OAAI

Schnack, HG; Bakker, SC; van't Slot, R; Groot, BM; Sinke, RJ; Kahn, RS; Pearson, PL

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CTLA4+49 A/G and CT60 polymorphisms in Dutch coeliac disease patients

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2004-06-16