Aayushi Srivastava

Heidelberg, BW 69120, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

Intratumoral IDH1 mutation status in intrahepatic cholangiocarcinoma is homogeneous.

Intratumoral IDH1 mutation status in intrahepatic cholangiocarcinoma is homogeneous.

Journal: Histopathology

Published: June 29, 2026

Prioritization of predisposition genes for familial non-medullary thyroid cancer by whole-genome sequencing.

Prioritization of predisposition genes for familial non-medullary thyroid cancer by whole-genome sequencing.

Journal: European journal of endocrinology

Published: October 08, 2024

Evaluation of a medical student-delivered smoking prevention program utilizing a face-aging mobile app for secondary schools in Germany: The Education Against Tobacco cluster-randomized controlled trial.

Evaluation of a medical student-delivered smoking prevention program utilizing a face-aging mobile app for secondary schools in Germany: The Education Against Tobacco cluster-randomized controlled trial.

Journal: European journal of cancer (Oxford, England : 1990)

Published: June 09, 2024

Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer.

Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer.

Journal: International journal of molecular sciences

Published: December 22, 2021

Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer.

Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer.

Journal: Molecular genetics and genomics : MGG

Published: April 21, 2021

A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer.

A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer.

Journal: Journal of personalized medicine

Published: February 25, 2021

Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer.

Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer.

Journal: International journal of molecular sciences

Published: January 22, 2021

Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer.

Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer.

Journal: Frontiers in endocrinology

Published: August 30, 2020

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer.

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer.

Journal: Cancers

Published: May 05, 2020

Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example.

Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example.

Journal: Hereditary cancer in clinical practice

Published: May 02, 2020

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing.

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing.

Journal: Frontiers in bioengineering and biotechnology

Published: December 03, 2019

Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways.

Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways.

Journal: Biomolecules

Published: August 29, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026