Ingegerd Elvers

Stockholm, AB, Sweden

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation.

The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation.

Journal: Genome medicine

Published: May 31, 2025

PIK3CA is recurrently mutated in canine mammary tumors, similarly to in human mammary neoplasia.

PIK3CA is recurrently mutated in canine mammary tumors, similarly to in human mammary neoplasia.

Journal: Scientific reports

Published: June 27, 2022

Genomically Complex Human Angiosarcoma and Canine Hemangiosarcoma Establish Convergent Angiogenic Transcriptional Programs Driven by Novel Gene Fusions.

Genomically Complex Human Angiosarcoma and Canine Hemangiosarcoma Establish Convergent Angiogenic Transcriptional Programs Driven by Novel Gene Fusions.

Journal: Molecular cancer research : MCR

Published: October 23, 2020

Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors.

Genome-wide association analysis of canine T zone lymphoma identifies link to hypothyroidism and a shared association with mast-cell tumors.

Journal: BMC genomics

Published: October 04, 2019

Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma.

Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma.

Journal: Molecular cancer research : MCR

Published: February 22, 2019

SETD2 Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma.

SETD2 Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma.

Journal: Cancer research

Published: November 20, 2017

Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression.

Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression.

Journal: Human genetics

Published: December 10, 2015

Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours.

Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours.

Journal: PLoS genetics

Published: September 11, 2015

Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.

Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.

Journal: Cell

Published: August 11, 2015

Exome sequencing of lymphomas from three dog breeds reveals somatic mutation patterns reflecting genetic background.

Exome sequencing of lymphomas from three dog breeds reveals somatic mutation patterns reflecting genetic background.

Journal: Genome research

Published: May 13, 2015

Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers.

Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers.

Journal: PLoS genetics

Published: September 03, 2014

Damage-induced DNA replication stalling relies on MAPK-activated protein kinase 2 activity.

Damage-induced DNA replication stalling relies on MAPK-activated protein kinase 2 activity.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: October 02, 2013

Showing 1-12 of 15

Last Updated: 09/26/2026