List of works - Susan L Slager

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

scientific article

A mega-analysis of genome-wide association studies for major depressive disorder

scientific article

Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing

scientific article

Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene

scientific article published in 2000

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

scientific article published on April 2013

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

scientific article published in April 2013

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

scientific article

Prediction of breast cancer risk based on profiling with common genetic variants

scientific article published on 8 April 2015

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

scientific article

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

scientific article published on 30 October 2011

A genomewide association study of citalopram response in major depressive disorder

scientific article

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

scientific article (publication date: February 2011)

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

scientific article (publication date: 2013)

Cigarette smoking and colorectal cancer risk by molecularly defined subtypes

scientific article

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

scientific article

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

scientific journal article

Investigation of serotonin-related genes in antidepressant response

scientific article published in September 2004

Mutations in CHEK2 associated with prostate cancer risk

scientific article published on 17 January 2003

Vitamin D insufficiency and prognosis in non-Hodgkin's lymphoma.

scientific article

An autosomal genomic screen for autism. Collaborative linkage study of autism

scientific article (publication date: 15 December 1999)

Event-free survival at 24 months is a robust end point for disease-related outcome in diffuse large B-cell lymphoma treated with immunochemotherapy.

scientific article published on 18 February 2014

Family history of hematopoietic malignancies and risk of non-Hodgkin lymphoma (NHL): a pooled analysis of 10 211 cases and 11 905 controls from the International Lymphoma Epidemiology Consortium (InterLymph).

scientific article published on 21 December 2006

Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

scientific article

Sequence analysis of the serotonin transporter and associations with antidepressant response

scientific article

Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

scientific article

Etiologic heterogeneity among non-Hodgkin lymphoma subtypes: the InterLymph Non-Hodgkin Lymphoma Subtypes Project

scientific article published in August 2014

Rates and Outcomes of Follicular Lymphoma Transformation in the Immunochemotherapy Era: A Report From the University of Iowa/Mayo Clinic Specialized Program of Research Excellence Molecular Epidemiology Resource

scientific article published on July 29, 2013

Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma

scientific article

Evaluation of candidate genes in case-control studies: a statistical method to account for related subjects

scientific article

Pharmacokinetic genes do not influence response or tolerance to citalopram in the STAR*D sample

scientific article

Analysis of association between the serotonin transporter and antidepressant response in a large clinical sample

scientific article

Comorbid conditions and survival in unselected, newly diagnosed patients with chronic lymphocytic leukemia

scientific article published on January 2008

Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium

scientific article

LEF-1 is a prosurvival factor in chronic lymphocytic leukemia and is expressed in the preleukemic state of monoclonal B-cell lymphocytosis

scientific article

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

scientific article published on 9 December 2013

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

scientific article published on 15 August 2011

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

scientific article

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL

scientific journal article

Diffuse large B-cell lymphoma (Richter syndrome) in patients with chronic lymphocytic leukaemia (CLL): a cohort study of newly diagnosed patients

scientific article

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

scientific article

Case-control studies of genetic markers: power and sample size approximations for Armitage's test for trend

scientific article published in January 2001

Non-Hodgkin lymphoma and obesity: a pooled analysis from the InterLymph Consortium

scientific article published on May 2008

Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

journal article published in 2015

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

scientific article published on 13 February 2012

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

scientific article

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

scientific article

B-cell count and survival: differentiating chronic lymphocytic leukemia from monoclonal B-cell lymphocytosis based on clinical outcome

scientific article

GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma

scientific article

Brief report: natural history of individuals with clinically recognized monoclonal B-cell lymphocytosis compared with patients with Rai 0 chronic lymphocytic leukemia

scientific article published on 20 July 2009

List of works by Susan L Slager

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

A mega-analysis of genome-wide association studies for major depressive disorder

Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing

Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Prediction of breast cancer risk based on profiling with common genetic variants

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

A genomewide association study of citalopram response in major depressive disorder

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Cigarette smoking and colorectal cancer risk by molecularly defined subtypes

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

Investigation of serotonin-related genes in antidepressant response

Mutations in CHEK2 associated with prostate cancer risk

Vitamin D insufficiency and prognosis in non-Hodgkin's lymphoma.

An autosomal genomic screen for autism. Collaborative linkage study of autism

Event-free survival at 24 months is a robust end point for disease-related outcome in diffuse large B-cell lymphoma treated with immunochemotherapy.

Family history of hematopoietic malignancies and risk of non-Hodgkin lymphoma (NHL): a pooled analysis of 10 211 cases and 11 905 controls from the International Lymphoma Epidemiology Consortium (InterLymph).

Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

Sequence analysis of the serotonin transporter and associations with antidepressant response

Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

Etiologic heterogeneity among non-Hodgkin lymphoma subtypes: the InterLymph Non-Hodgkin Lymphoma Subtypes Project

Rates and Outcomes of Follicular Lymphoma Transformation in the Immunochemotherapy Era: A Report From the University of Iowa/Mayo Clinic Specialized Program of Research Excellence Molecular Epidemiology Resource

Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma

Evaluation of candidate genes in case-control studies: a statistical method to account for related subjects

Pharmacokinetic genes do not influence response or tolerance to citalopram in the STAR*D sample

Analysis of association between the serotonin transporter and antidepressant response in a large clinical sample

Comorbid conditions and survival in unselected, newly diagnosed patients with chronic lymphocytic leukemia

Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium

LEF-1 is a prosurvival factor in chronic lymphocytic leukemia and is expressed in the preleukemic state of monoclonal B-cell lymphocytosis

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL

Diffuse large B-cell lymphoma (Richter syndrome) in patients with chronic lymphocytic leukaemia (CLL): a cohort study of newly diagnosed patients

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

Case-control studies of genetic markers: power and sample size approximations for Armitage's test for trend

Non-Hodgkin lymphoma and obesity: a pooled analysis from the InterLymph Consortium

Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

B-cell count and survival: differentiating chronic lymphocytic leukemia from monoclonal B-cell lymphocytosis based on clinical outcome

GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma

Brief report: natural history of individuals with clinically recognized monoclonal B-cell lymphocytosis compared with patients with Rai 0 chronic lymphocytic leukemia