Layal Yasin

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 12 publications

A machine learning framework for predictive interpretation of variants of uncertain significance in hereditary cancer.

A machine learning framework for predictive interpretation of variants of uncertain significance in hereditary cancer.

Journal: Frontiers in systems biology

Published: March 11, 2026

Germline variants observed in pediatric cancer patients related to hereditary breast and ovarian cancer in adults.

Germline variants observed in pediatric cancer patients related to hereditary breast and ovarian cancer in adults.

Journal: International journal of cancer

Published: September 17, 2024

Benchmarking whole exome sequencing in the German network for personalized medicine.

Benchmarking whole exome sequencing in the German network for personalized medicine.

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

Published: June 20, 2024

Do it once, but do it right.

Do it once, but do it right.

Journal: Haematologica

Published: March 05, 2024

Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants.

Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants.

Journal: HemaSphere

Published: October 12, 2023

Co-targeting HSP90 alpha and CDK7 overcomes resistance against HSP90 inhibitors in BCR-ABL1+ leukemia cells.

Co-targeting HSP90 alpha and CDK7 overcomes resistance against HSP90 inhibitors in BCR-ABL1+ leukemia cells.

Journal: Cell death & disease

Published: June 06, 2023

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia.

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia.

Journal: HemaSphere

Published: January 31, 2023

Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies.

Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies.

Journal: Frontiers in pediatrics

Published: October 26, 2022

Clinical and immunophenotypic characteristics of familial leukemia predisposition caused by PAX5 germline variants.

Clinical and immunophenotypic characteristics of familial leukemia predisposition caused by PAX5 germline variants.

Journal: Leukemia

Published: March 01, 2022

Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents.

Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents.

Journal: Journal of pediatric hematology/oncology

Published: November 11, 2021

Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer.

Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer.

Journal: European journal of human genetics : EJHG

Published: January 12, 2021

Penetrance and Expressivity in Inherited Cancer Predisposing Syndromes.

Penetrance and Expressivity in Inherited Cancer Predisposing Syndromes.

Journal: Trends in cancer

Published: July 09, 2018

Showing 1-12 of 12

Last Updated: 09/26/2026