Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Jeremy Chimene-Weiss

Exome Sequencing of African-American Prostate Cancer Reveals Loss-Of-Function ERF Mutations

Cancer Discovery

Oncology

2017

English

Bromodomain Inhibition Reveals FGF15/19 as a Target of Epigenetic Regulation and Metabolic Control

2019

English

Related publications

Family-Based Whole-Exome Sequencing Identifies Novel Loss-Of-Function Mutations of FBN1 for Marfan Syndrome

English

African American Exome Sequencing Identifies Potential Risk Variants at Alzheimer Disease Loci

English

Mp39-18 Higher Frequency of Germline Brca1 and Brca2 Mutations in African American Prostate Cancer

Journal of Urology

Urology

2016

English

Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing

BMC Medical Genetics

Genetics

2014

English

Understanding Prostate Cancer in African-American Men

Cancer Discovery

Oncology

2018

English

Whole Genome Sequencing Reveals Elevated Tumor Mutational Burden and Initiating Driver Mutations in African Men With Treatment-Naive, High-Risk Prostate Cancer

Cancer Research

Oncology

2018

English

Exome and Genome Sequencing of Nasopharynx Cancer Identifies NF-κB Pathway Activating Mutations

Nature Communications

English

1295 Discovery of Filaggrin Loss-Of-Function Mutations R788X in Hispanic and S3640X in African-American/Native American Children With Atopic Dermatitis

Journal of Investigative Dermatology

English

Exome Sequencing Reveals Germline Gain-Of-Function EGFR Mutation in an Adult With Lhermitte-Duclos Disease

Cold Spring Harbor molecular case studies

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Jeremy Chimene-Weiss

Exome Sequencing of African-American Prostate Cancer Reveals Loss-Of-Function ERF Mutations

Bromodomain Inhibition Reveals FGF15/19 as a Target of Epigenetic Regulation and Metabolic Control

Related publications

Family-Based Whole-Exome Sequencing Identifies Novel Loss-Of-Function Mutations of FBN1 for Marfan Syndrome

African American Exome Sequencing Identifies Potential Risk Variants at Alzheimer Disease Loci

Mp39-18 Higher Frequency of Germline Brca1 and Brca2 Mutations in African American Prostate Cancer

Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing

Understanding Prostate Cancer in African-American Men

Whole Genome Sequencing Reveals Elevated Tumor Mutational Burden and Initiating Driver Mutations in African Men With Treatment-Naive, High-Risk Prostate Cancer

Exome and Genome Sequencing of Nasopharynx Cancer Identifies NF-κB Pathway Activating Mutations

1295 Discovery of Filaggrin Loss-Of-Function Mutations R788X in Hispanic and S3640X in African-American/Native American Children With Atopic Dermatitis

Exome Sequencing Reveals Germline Gain-Of-Function EGFR Mutation in an Adult With Lhermitte-Duclos Disease