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Cancer risks among BRCA1 and BRCA2 mutation carriers

British journal of cancer, 2007-01, Vol.96 (1), p.11-15

2007

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Risk reduction and screening of cancer in hereditary breast-ovarian cancer syndromes: ESMO Clinical Practice Guideline

Annals of oncology, 2023-01, Vol.34 (1), p.33-47

2023

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Secreted amyloid β-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease

Nature medicine, 1996-08, Vol.2 (8), p.864-870

1996

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A Single Nucleotide Polymorphism in the RAD51 Gene Modifies Cancer Risk in BRCA2 but Not BRCA1 Carriers

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (6), p.3232-3236

2001

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BRCA carriers after risk-reducing bilateral salpingo-oophorectomy: menopausal hormone therapy knowledge gaps, and the impact of physicians' recommendations

Climacteric : the journal of the International Menopause Society, 2023-04, Vol.26 (2), p.154-160

2023

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Common founder BRCA2 pathogenic variants and breast cancer characteristics in Ethiopian Jews

Breast cancer research and treatment, 2022-05, Vol.193 (1), p.217-224

2022

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Genetic factors in Alzheimer's disease: A review of recent advances

Annals of neurology, 1996-12, Vol.40 (6), p.829-840

1996

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Precision medicine meets public health: population screening for BRCA1 and BRCA2

JNCI : Journal of the National Cancer Institute, 2015-01, Vol.107 (1), p.420-dju420

2015

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Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1

Human reproduction (Oxford), 2006-08, Vol.21 (8), p.2047-2051

2006

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O-22 Embryo biopsy for PGD has no significant impact on neonatal outcome

Reproductive biomedicine online, 2013-05, Vol.26, p.S22-S22

2013

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P-2 Overcoming limitations of single cell analysis in duplicated and GC-rich genomic regions using multiple displacement amplification for preimplantation genetic diagnosis (PGD)

Reproductive biomedicine online, 2013-05, Vol.26, p.S27-S28

2013

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Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance

Gastroenterology (New York, N.Y. 1943), 2017-06, Vol.152 (8), p.1876-1880.e1

2017

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Amyloid (Aβ) deposition in chromosome 1-linked Alzheimer's disease: The volga german families

Annals of neurology, 1997-01, Vol.41 (1), p.52-57

1997

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O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism

Reproductive biomedicine online, 2010, Vol.20, p.S15-S15

2010

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Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates

The Lancet (British edition), 2000-08, Vol.356 (9230), p.652-653

2000

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Successful polar body-based preimplantation genetic diagnosis for achondroplasia

Reproductive biomedicine online, 2008, Vol.16 (2), p.276-282

2008

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O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible

Reproductive biomedicine online, 2010, Vol.20, p.S17-S17

2010

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Replacement therapy with imiglucerase for type 1 Gaucher's disease

The Lancet (British edition), 1995-06, Vol.345 (8963), p.1479-1480

1995

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Gilbert Syndrome and Glucose-6-Phosphate Dehydrogenase Deficiency: A Dose-Dependent Genetic Interaction Crucial to Neonatal Hyperbilirubinemia

Proceedings of the National Academy of Sciences - PNAS, 1997-10, Vol.94 (22), p.12128-12132

1997

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Monogenic determinants of familial Alzheimer's disease: presenilin-2 mutations

Cellular and molecular life sciences : CMLS, 1998-09, Vol.54 (9), p.910-919

1998

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Polar Body-Based Preimplantation Genetic Diagnosis for N-Acetylglutamate Synthase Deficiency

Fetal diagnosis and therapy, 2008-01, Vol.24 (3), p.170-176

2008

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PGD for fragile X syndrome: ovarian function is the main determinant of success

Human reproduction (Oxford), 2010-10, Vol.25 (10), p.2629-2636

2010

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Familial Clustering of Site-Specific Cancer Risks Associated with BRCA1 and BRCA2 Mutations in the Ashkenazi Jewish Population

Proceedings of the National Academy of Sciences - PNAS, 2006-03, Vol.103 (10), p.3770-3774

2006

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High frequency of factor V Leiden in a population of Israeli Arabs

Thrombosis and haemostasis, 1999-12, Vol.82 (6), p.1768-1768

1999

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Cancer risks among BRCA1 and BRCA2 mutation carriers

Risk reduction and screening of cancer in hereditary breast-ovarian cancer syndromes: ESMO Clinical Practice Guideline

Secreted amyloid β-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease

A Single Nucleotide Polymorphism in the RAD51 Gene Modifies Cancer Risk in BRCA2 but Not BRCA1 Carriers

BRCA carriers after risk-reducing bilateral salpingo-oophorectomy: menopausal hormone therapy knowledge gaps, and the impact of physicians' recommendations

Common founder BRCA2 pathogenic variants and breast cancer characteristics in Ethiopian Jews

Genetic factors in Alzheimer's disease: A review of recent advances

Precision medicine meets public health: population screening for BRCA1 and BRCA2

Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1

O-22 Embryo biopsy for PGD has no significant impact on neonatal outcome

P-2 Overcoming limitations of single cell analysis in duplicated and GC-rich genomic regions using multiple displacement amplification for preimplantation genetic diagnosis (PGD)

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance

Amyloid (Aβ) deposition in chromosome 1-linked Alzheimer's disease: The volga german families

O1 Preimplantation Genetic Diagnosis (PGD) for germline mosaicism

Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates

Successful polar body-based preimplantation genetic diagnosis for achondroplasia

New ISSCR guidelines underscore major principles for responsible translational stem cell research

O8 Preimplantation genetic diagnosis (PGD) for monogenic disorders. When blastomere analysis may be impossible

Replacement therapy with imiglucerase for type 1 Gaucher's disease

Gilbert Syndrome and Glucose-6-Phosphate Dehydrogenase Deficiency: A Dose-Dependent Genetic Interaction Crucial to Neonatal Hyperbilirubinemia

Monogenic determinants of familial Alzheimer's disease: presenilin-2 mutations

Polar Body-Based Preimplantation Genetic Diagnosis for N-Acetylglutamate Synthase Deficiency

PGD for fragile X syndrome: ovarian function is the main determinant of success

Familial Clustering of Site-Specific Cancer Risks Associated with BRCA1 and BRCA2 Mutations in the Ashkenazi Jewish Population

High frequency of factor V Leiden in a population of Israeli Arabs

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