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1
BRCA1 Basal-like Breast Cancers Originate from Luminal Epithelial Progenitors and Not from Basal Stem Cells
BRCA1 Basal-like Breast Cancers Originate from Luminal Epithelial Progenitors and Not from Basal Stem Cells
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BRCA1 Basal-like Breast Cancers Originate from Luminal Epithelial Progenitors and Not from Basal Stem Cells

Cell stem cell, 2010-09, Vol.7 (3), p.403-417 [Peer Reviewed Journal]

2010 Elsevier Inc. ;2015 INIST-CNRS ;Copyright 2010 Elsevier Inc. All rights reserved. ;ISSN: 1934-5909 ;EISSN: 1875-9777 ;DOI: 10.1016/j.stem.2010.07.010 ;PMID: 20804975

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2
Genetic Predisposition Directs Breast Cancer Phenotype by Dictating Progenitor Cell Fate
Genetic Predisposition Directs Breast Cancer Phenotype by Dictating Progenitor Cell Fate
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Genetic Predisposition Directs Breast Cancer Phenotype by Dictating Progenitor Cell Fate

Cell stem cell, 2011-02, Vol.8 (2), p.149-163 [Peer Reviewed Journal]

2011 Elsevier Inc. ;2015 INIST-CNRS ;Copyright © 2011 Elsevier Inc. All rights reserved. ;ISSN: 1934-5909 ;EISSN: 1875-9777 ;DOI: 10.1016/j.stem.2010.12.007 ;PMID: 21295272

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3
Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte
Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte
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Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

American journal of human genetics, 2011-09, Vol.89 (3), p.451-458 [Peer Reviewed Journal]

2011 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2011 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Sep 9, 2011 ;2011 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2011 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2011.08.002 ;PMID: 21885028 ;CODEN: AJHGAG

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4
Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
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Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

American journal of human genetics, 2012-04, Vol.90 (4), p.734-739 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Apr 6, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.02.027 ;PMID: 22464251 ;CODEN: AJHGAG

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5
A Mammary Stem Cell Population Identified and Characterized in Late Embryogenesis Reveals Similarities to Human Breast Cancer
A Mammary Stem Cell Population Identified and Characterized in Late Embryogenesis Reveals Similarities to Human Breast Cancer
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A Mammary Stem Cell Population Identified and Characterized in Late Embryogenesis Reveals Similarities to Human Breast Cancer

Cell stem cell, 2012-02, Vol.10 (2), p.183-197 [Peer Reviewed Journal]

2012 Elsevier Inc. ;2015 INIST-CNRS ;Copyright © 2012 Elsevier Inc. All rights reserved. ;2012 ll Press. All rights reserved. 2012 ;ISSN: 1934-5909 ;EISSN: 1875-9777 ;DOI: 10.1016/j.stem.2011.12.018 ;PMID: 22305568

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6
A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes
A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes
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A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

American journal of human genetics, 2007-11, Vol.81 (5), p.873-883 [Peer Reviewed Journal]

2007 The American Society of Human Genetics ;2007 INIST-CNRS ;Copyright University of Chicago, acting through its Press Nov 2007 ;2007 by The American Society of Human Genetics. All rights reserved. 2007 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/521032 ;PMID: 17924331 ;CODEN: AJHGAG

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7
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation
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A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation

American journal of human genetics, 2011-03, Vol.88 (3), p.351-361 [Peer Reviewed Journal]

2011 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2011 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Mar 11, 2011 ;Distributed under a Creative Commons Attribution 4.0 International License ;2011 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2011 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2011.02.007 ;PMID: 21397064 ;CODEN: AJHGAG

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8
Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies
Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies
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Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies

American journal of human genetics, 2003-05, Vol.72 (5), p.1117-1130 [Peer Reviewed Journal]

2003 The American Society of Human Genetics ;2003 INIST-CNRS ;2003 by The American Society of Human Genetics. All rights reserved. 2003 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/375033 ;PMID: 12677558 ;CODEN: AJHGAG

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9
Another Case of Imprinting Defect in a Girl with Angelman Syndrome Who Was Conceived by Intracytoplasmic Sperm Injection
Another Case of Imprinting Defect in a Girl with Angelman Syndrome Who Was Conceived by Intracytoplasmic Sperm Injection
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Another Case of Imprinting Defect in a Girl with Angelman Syndrome Who Was Conceived by Intracytoplasmic Sperm Injection

American journal of human genetics, 2003, Vol.72 (1), p.218-219 [Peer Reviewed Journal]

2003 The American Society of Human Genetics ;2003 INIST-CNRS ;2003 by The American Society of Human Genetics. All rights reserved. 2003 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/346030 ;PMID: 12549484 ;CODEN: AJHGAG

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10
Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
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Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

American journal of human genetics, 2008-04, Vol.82 (4), p.937-948 [Peer Reviewed Journal]

2008 The American Society of Human Genetics ;2008 INIST-CNRS ;Copyright University of Chicago, acting through its Press Apr 11, 2008 ;2008 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved.. 2008 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2008.02.008 ;PMID: 18355772 ;CODEN: AJHGAG

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11
Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein
Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein
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Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein

American journal of human genetics, 2009-04, Vol.84 (4), p.505-510 [Peer Reviewed Journal]

2009 The American Society of Human Genetics ;2009 INIST-CNRS ;2009 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2009 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2009.03.004 ;PMID: 19344877 ;CODEN: AJHGAG

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12
Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer
Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer
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Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer

American journal of human genetics, 2009-10, Vol.85 (4), p.427-446 [Peer Reviewed Journal]

2009 The American Society of Human Genetics ;2009 INIST-CNRS ;Copyright University of Chicago, acting through its Press Oct 9, 2009 ;2009 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved.. 2009 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2009.08.018 ;PMID: 19781682 ;CODEN: AJHGAG

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13
Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia
Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia
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Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia

American journal of human genetics, 2007-10, Vol.81 (4), p.813-820 [Peer Reviewed Journal]

2007 The American Society of Human Genetics ;2007 INIST-CNRS ;Distributed under a Creative Commons Attribution 4.0 International License ;2007 by The American Society of Human Genetics. All rights reserved. 2007 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/521314 ;PMID: 17847006 ;CODEN: AJHGAG

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14
RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies
RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies
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RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies

American journal of human genetics, 2007-12, Vol.81 (6), p.1186-1200 [Peer Reviewed Journal]

2007 The American Society of Human Genetics ;2008 INIST-CNRS ;Copyright University of Chicago, acting through its Press Dec 2007 ;Distributed under a Creative Commons Attribution 4.0 International License ;2007 by The American Society of Human Genetics. All rights reserved. 2007 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/522611 ;PMID: 17999359 ;CODEN: AJHGAG

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15
Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects
Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects
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Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects

American journal of human genetics, 2002-07, Vol.71 (1), p.162-164 [Peer Reviewed Journal]

2002 The American Society of Human Genetics ;2002 INIST-CNRS ;2002 by The American Society of Human Genetics. All rights reserved. 2002 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/341096 ;PMID: 12016591 ;CODEN: AJHGAG

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16
CHEK21100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies
CHEK21100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies
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CHEK21100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies

American journal of human genetics, 2004-06, Vol.74 (6), p.1175-1182 [Peer Reviewed Journal]

2004 The American Society of Human Genetics ;2004 INIST-CNRS ;2004 by The American Society of Human Genetics. All rights reserved. 2004 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/421251 ;PMID: 15122511 ;CODEN: AJHGAG

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17
Multifactor-Dimensionality Reduction Reveals High-Order Interactions among Estrogen-Metabolism Genes in Sporadic Breast Cancer
Multifactor-Dimensionality Reduction Reveals High-Order Interactions among Estrogen-Metabolism Genes in Sporadic Breast Cancer
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Multifactor-Dimensionality Reduction Reveals High-Order Interactions among Estrogen-Metabolism Genes in Sporadic Breast Cancer

American journal of human genetics, 2001-07, Vol.69 (1), p.138-147 [Peer Reviewed Journal]

2001 The American Society of Human Genetics ;2001 INIST-CNRS ;2001 by The American Society of Human Genetics. All rights reserved. 2001 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/321276 ;PMID: 11404819 ;CODEN: AJHGAG

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18
Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
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Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families

American journal of human genetics, 1998-03, Vol.62 (3), p.676-689 [Peer Reviewed Journal]

1998 The American Society of Human Genetics ;1998 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/301749 ;CODEN: AJHGAG

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19
Breast and ovarian cancer incidence in BRCA1-mutation carriers
Breast and ovarian cancer incidence in BRCA1-mutation carriers
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Breast and ovarian cancer incidence in BRCA1-mutation carriers

American journal of human genetics, 1995, Vol.56 (1), p.265-271 [Peer Reviewed Journal]

1995 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;CODEN: AJHGAG

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20
A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia
A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia
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A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia

American journal of human genetics, 2012-05, Vol.90 (5), p.900-906 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 4, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.04.001 ;PMID: 22541561 ;CODEN: AJHGAG

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