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Stephen W Scherer
Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada

Faculty Member: Genomics & Genetics > Genomics [ since 29 July 2004 ]
[ Evaluations ]
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Evaluations

The Fine-Scale and Complex Architecture of Human Copy-Number Variation.
Perry GH, Ben-Dor A, …, Bruhn L, Lee C
Am J Hum Genet 2008 Jan 24 [abstract on PubMed] [related articles] [full text]
Selected by | Stephen Scherer
Evaluated 6 Mar 2008

Association between Microdeletion and Microduplication at 16p11.2 and Autism.
Weiss LA, Shen Y, …, Daly MJ, the Autism Consortium
N Engl J Med 2008 Jan 9 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Stephen Scherer / Sue Malcolm
Evaluated 24 Jan 2008

Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.
Jiang Z, Tang H, …, Pevzner PA, Eichler EE
Nat Genet 2007 Nov 39(11):1361-8 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Stephen Scherer
Evaluated 17 Oct 2007

Strong association of de novo copy number mutations with autism.
Sebat J, Lakshmi B, …, Ye K, Wigler M
Science 2007 Apr 20 316(5823):445-9 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Stephen Scherer / James Fry / Andrey Rzhetsky / John Rubenstein / Guoping Feng
Evaluated 13 Apr 2007


Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome.
Weber M, Hellmann I, …, Rebhan M, Schübeler D
Nat Genet 2007 Apr 39(4):457-66 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Stephen Scherer
Evaluated 19 Mar 2007

In vivo enhancer analysis of human conserved non-coding sequences.
Pennacchio LA, Ahituv N, …, Visel A, Rubin EM
Nature 2006 Nov 23 444(7118):499-502 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Stephen Scherer / Kenneth Campbell / Jason Lieb
Evaluated 1 Dec 2006

An initial map of insertion and deletion (INDEL) variation in the human genome.
Mills RE, Luttig CT, …, Pittard WS, Devine SE
Genome Res 2006 Sep 16(9):1182-90 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Stephen Scherer
Evaluated 31 Aug 2006

Common deletion polymorphisms in the human genome.
McCarroll SA, Hadnott TN, …, Altshuler DM, International HapMap Consortium
Nat Genet 2006 Jan 38(1):86-92 [abstract on PubMed] [related articles] [order article]
Selected by | Karin Schmitt / Emmanouil Dermitzakis / Stephen Scherer / Yasushi Okazaki
Evaluated 19 Jan 2006

A high-resolution survey of deletion polymorphism in the human genome.
Conrad DF, Andrews TD, …, Hurles ME, Pritchard JK
Nat Genet 2006 Jan 38(1):75-81 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Emmanouil Dermitzakis / Chris Ponting / Pui-Yan Kwok / Stephen Scherer
Evaluated 19 Jan 2006

Common deletions and SNPs are in linkage disequilibrium in the human genome.
Hinds DA, Kloek AP, …, Chen X, Frazer KA
Nat Genet 2006 Jan 38(1):82-5 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Emmanouil Dermitzakis / Pui-Yan Kwok / Stephen Scherer
Evaluated 19 Jan 2006

A haplotype map of the human genome.
International HapMap Consortium
Nature 2005 Oct 27 437(7063):1299-320 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Vivian Cheung / Stephen Scherer
Evaluated 25 Nov 2005

Diagnostic genome profiling in mental retardation.
de Vries BB, Pfundt R, …, Brunner HG, Veltman JA
Am J Hum Genet 2005 Oct 77(4):606-16 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Stephen Scherer
Evaluated 19 Sep 2005

Epigenetic differences arise during the lifetime of monozygotic twins.
Fraga MF, Ballestar E, …, Plass C, Esteller M
Proc Natl Acad Sci U S A 2005 Jul 26 102(30):10604-9 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Alain Ghysen / Charles Auffray / Stephen Scherer / Thomas Jenuwein
Evaluated 4 Aug 2005

Fine-scale structural variation of the human genome.
Tuzun E, Sharp AJ, …, Olson MV, Eichler EE
Nat Genet 2005 Jul 37(7):727-32 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Stephen Scherer / Sue Malcolm / Karin Schmitt / Ulf Pettersson / Barbara Trask / Tony Long
Evaluated 24 May 2005

A common inversion under selection in Europeans.
Stefansson H, Helgason A, …, Kong A, Stefansson K
Nat Genet 2005 Feb 37(2):129-37 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Jonathan Pritchard / Stephen Scherer / Ulf Pettersson
Evaluated 23 Feb 2005

High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization.
Zhang X, Snijders A, …, Bolund L, Pinkel D
Am J Hum Genet 2005 Feb 76(2):312-26 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Stephen Scherer
Evaluated 21 Jan 2005

Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion.
Visser R, Shimokawa O, …, Niikawa N, Matsumoto N
Am J Hum Genet 2005 Jan 76(1):52-67 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Stephen Scherer
Evaluated 17 Dec 2004

Complex SNP-related sequence variation in segmental genome duplications.
Fredman D, White SJ, …, Den Dunnen JT, Brookes AJ
Nat Genet 2004 Aug 36(8):861-6 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Stephen Scherer / Magnus Nordborg
Evaluated 4 Oct 2004

Large-scale copy number polymorphism in the human genome.
Sebat J, Lakshmi B, …, Zetterberg A, Wigler M
Science 2004 Jul 23 305(5683):525-8 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Andrew Wilkie / Michael O'Donovan / Stephen Scherer / Andrey Rzhetsky / Niklas Dahl / Andrew Belmont
Evaluated 23 Sep 2004

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