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Prevalence of germline pathogenic variants in 22 cancer susceptibility genes in Swedish pediatric cancer patients

Scientific reports, 2021-03, Vol.11 (1), p.5307-5307, Article 5307

2021

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A century of Hereditas: from local publication to international journal

Hereditas, 2020-12, Vol.157 (1), p.50-50, Article 50

2020

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Genetic testing in women with early-onset breast cancer: a Traceback pilot study

Breast cancer research and treatment, 2021-11, Vol.190 (2), p.307-315

2021

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A stroke gene panel for whole-exome sequencing

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.317-324

2019

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Correction to: A century of Hereditas: from local publication to international journal

Hereditas, 2021-02, Vol.158 (1), p.8-8, Article 8

2021

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Rare diseases: past achievements and future prospects

Journal of community genetics, 2021-04, Vol.12 (2), p.205-206

2021

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The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer

Gynecologic oncology, 2006-05, Vol.101 (2), p.238-243

2006

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From Mendel to Medical Genetics

European journal of human genetics : EJHG, 2017-12, Vol.25 (s2), p.S53-S59

2017

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From Mendel to Medical Genetics

European journal of human genetics : EJHG, 2017-12, Vol.25 (s2)

2017

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Utvidgad anlagsbärartestning kan bredda fosterdiagnostiken - Recessiva sjukdomsanlag kan kartläggas hos friska personer inför planerad graviditet

Läkartidningen, 2018, Vol.115 (6), p.234

Kristoffersson, Ulf

2018

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Diagnosing Monogenic Stroke at Younger Age

Stroke (1970), 2024-11

2024

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Pregnancy Planning and Genetic Testing: Exploring Advantages, and Challenges

Genes, 2024-09, Vol.15 (9), p.1205

2024

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A stroke gene panel for whole-exome sequencing

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.317-324

2019

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Abstract 2548: Cancer in first-degree relatives of women with early-onset breast cancer: a comparison of self-reported and cancer registry data

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.2548-2548

2016

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Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72

BMC medical genetics, 2008-11, Vol.9 (1), p.101-101, Article 101

2008

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Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

Stroke (1970), 2020-04, Vol.51 (4), p.1056-1063

2020

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Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of stroke

European journal of human genetics : EJHG, 2023-02, Vol.31 (2), p.239-242

2023

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Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer

Acta oncologica, 2018-05, Vol.57 (5), p.595-603

2018

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Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer

JAMA : the journal of the American Medical Association, 2012-01, Vol.307 (4), p.382

2012

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Increased Cancer Risk in Families with Pediatric Cancer Is Associated with Gender, Age, Diagnosis, and Degree of Relation to the Child

Cancer epidemiology, biomarkers & prevention, 2020-11, Vol.29 (11), p.2171-2179

2020

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Abstract 2747: Increasing age at first full-time pregnancy correlates to use of oral contraceptives before age 20 in women with a family history of breast cancer

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.2747-2747

2015

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BRCAsearch: written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer

Breast cancer research and treatment, 2018-02, Vol.168 (1), p.117-126

2018

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Familial aggregation of stroke amongst young patients in Lund Stroke Register

European journal of neurology, 2016-02, Vol.23 (2), p.401-407

2016

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Regulatory Issues for Genetic Testing in Clinical Practice

Molecular biotechnology, 2008-09, Vol.40 (1), p.113-117

Kristoffersson, Ulf

2008

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Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer: A Population-Based Study in Southern Sweden

Public health genomics, 2020, Vol.23 (3-4), p.100-109

2020

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Prevalence of germline pathogenic variants in 22 cancer susceptibility genes in Swedish pediatric cancer patients

A century of Hereditas: from local publication to international journal

Genetic testing in women with early-onset breast cancer: a Traceback pilot study

A stroke gene panel for whole-exome sequencing

Correction to: A century of Hereditas: from local publication to international journal

Rare diseases: past achievements and future prospects

The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer

From Mendel to Medical Genetics

From Mendel to Medical Genetics

Utvidgad anlagsbärartestning kan bredda fosterdiagnostiken - Recessiva sjukdomsanlag kan kartläggas hos friska personer inför planerad graviditet

Diagnosing Monogenic Stroke at Younger Age

Pregnancy Planning and Genetic Testing: Exploring Advantages, and Challenges

A stroke gene panel for whole-exome sequencing

Abstract 2548: Cancer in first-degree relatives of women with early-onset breast cancer: a comparison of self-reported and cancer registry data

Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72

Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of stroke

Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer

Increased Cancer Risk in Families with Pediatric Cancer Is Associated with Gender, Age, Diagnosis, and Degree of Relation to the Child

Abstract 2747: Increasing age at first full-time pregnancy correlates to use of oral contraceptives before age 20 in women with a family history of breast cancer

BRCAsearch: written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer

Familial aggregation of stroke amongst young patients in Lund Stroke Register

Regulatory Issues for Genetic Testing in Clinical Practice

Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer: A Population-Based Study in Southern Sweden

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