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Trisomy Recurrence: A Reconsideration Based on North American Data

American journal of human genetics, 2004-09, Vol.75 (3), p.376-385

2004

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Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth

PLoS genetics, 2014-05, Vol.10 (5), p.e1004333

2014

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Chromosomal Aberrations in Cord Blood Are Associated with Prenatal Exposure to Carcinogenic Polycyclic Aromatic Hydrocarbons

Cancer epidemiology, biomarkers & prevention, 2005-02, Vol.14 (2), p.506-511

2005

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Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis

Proceedings of the National Academy of Sciences - PNAS, 2013-05, Vol.110 (19), p.7790-7795

2013

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Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss

Human genetics, 2014-04, Vol.133 (4), p.417-424

2014

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Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence

Annual review of genomics and human genetics, 2015-01, Vol.16 (1), p.309-326

2015

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Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres

Current biology, 1997-11, Vol.7 (11), p.901-904

1997

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Holoprosencephaly due to mutations in ZIC2 , a homologue of Drosophila odd-paired

Nature genetics, 1998-10, Vol.20 (2), p.180-183

1998

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Urinary Naphthol Metabolites and Chromosomal Aberrations in 5-Year-Old Children

Cancer epidemiology, biomarkers & prevention, 2012-07, Vol.21 (7), p.1191-1202

2012

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Trisomic Pregnancy and Earlier Age at Menopause

American journal of human genetics, 2000-08, Vol.67 (2), p.395-404

2000

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Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21

BMC medical genetics, 2006-03, Vol.7 (1), p.24-24, Article 24

2006

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Scrambling eggs in plastic bottles

PLoS genetics, 2007-01, Vol.3 (1), p.e6

2007

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Coding Mutations in p57 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors

American journal of human genetics, 1997-08, Vol.61 (2), p.295-303

1997

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Having It All

American journal of human genetics, 2007-10, Vol.81 (4), p.648-656

Warburton, Dorothy

2007

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Identification of a novel member of the TGF-beta superfamily highly expressed in human placenta

Gene, 1997-12, Vol.203 (1), p.17-26

1997

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Strong Association of De Novo Copy Number Mutations with Autism

Science (American Association for the Advancement of Science), 2007-04, Vol.316 (5823), p.445-449

2007

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De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

American journal of human genetics, 1991-11, Vol.49 (5), p.995-1013

Warburton, D

1991

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2006 William Allan Award Address. Having it all

American journal of human genetics, 2007-10, Vol.81 (4), p.648-656

Warburton, Dorothy

2007

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CANADIAN PIONEERS: F. Clarke Fraser

Genome, 2009-03, Vol.52 (3), p.iii-iv

Warburton, Dorothy

2009

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PIONNIERS CANADIENS : F. Clarke Fraser

Genome, 2009-03, Vol.52 (3), p.v-vi

Warburton, Dorothy

2009

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The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease

Human genetics, 2014-01, Vol.133 (1), p.11-27

2014

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The Congenital Heart Disease Genetic Network Study: Rationale, Design, and Early Results

Circulation research, 2013-02, Vol.112 (4), p.698-706

2013

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Molecular and Genetic Damage from Environmental Tobacco Smoke in Young Children

Cancer epidemiology, biomarkers & prevention, 1999-05, Vol.8 (5), p.427-431

1999

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genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

Proceedings of the National Academy of Sciences - PNAS, 2009-07, Vol.106 (29), p.12031-12036

2009

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Trisomy Recurrence: A Reconsideration Based on North American Data

Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth

Chromosomal Aberrations in Cord Blood Are Associated with Prenatal Exposure to Carcinogenic Polycyclic Aromatic Hydrocarbons

Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis

Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss

Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence

Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres

Holoprosencephaly due to mutations in ZIC2 , a homologue of Drosophila odd-paired

Urinary Naphthol Metabolites and Chromosomal Aberrations in 5-Year-Old Children

Trisomic Pregnancy and Earlier Age at Menopause

Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21

Scrambling eggs in plastic bottles

Coding Mutations in p57 Are Present in Some Cases of Beckwith-Wiedemann Syndrome but Are Rare or Absent in Wilms Tumors

Having It All

Identification of a novel member of the TGF-beta superfamily highly expressed in human placenta

Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

Strong Association of De Novo Copy Number Mutations with Autism

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

2006 William Allan Award Address. Having it all

CANADIAN PIONEERS: F. Clarke Fraser

PIONNIERS CANADIENS : F. Clarke Fraser

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease

The Congenital Heart Disease Genetic Network Study: Rationale, Design, and Early Results

Molecular and Genetic Damage from Environmental Tobacco Smoke in Young Children

genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

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