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The American Journal of Surgical Pathology
|
May 3, 2021
Pathology, Radiology, and Genetics of Interstitial Lung Disease in Patients With Shortened Telomeres
Matthew J Cecchini, Tara Tarmey, Allison Ferreira, et al.
Mayo Clinic Proceedings
|
July 2, 2019
Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained Cytopenias
Abhishek A Mangaonkar, Alejandro Ferrer, Filippo Pinto E Vairo, et al.
British Journal of Haematology
|
June 23, 2020
Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients
Antoine N Saliba, Alejandro Ferrer, Naseema Gangat, et al.
Haematologica
|
July 11, 2020
A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype
Laura Schultz-Rogers, Francis P Lach, Kimberly A Rickman, et al.
Blood Cancer Journal
|
November 18, 2020
Functional validation of TERT and TERC variants of uncertain significance in patients with short telomere syndromes
Alejandro Ferrer, Abhishek A Mangaonkar, Susanna Stroik, et al.
American Journal of Hematology
|
June 15, 2026
Promoter TERT-Related Hematopoietic Somatic Mosaicism in Patients With Telomere Biology Disorders
Madeline Franke, Rachel Kirchner, Bianca Barredo, et al.
Haematologica
|
December 4, 2025
Inherited DNA repair variants are associated with clonal hematopoiesis and cardiovascular risk in men with metastatic prostate cancer
Olisaemeka Ogbue, Yael Kusne, Osama Mosalem, et al.
British Journal of Haematology
|
March 5, 2025
Prevalence of cytopenia(s) and somatic variants in patients with DDX41 mutant germline predisposition syndrome
Yael Kusne, Talha Badar, Terra Lasho, et al.
Genomics, Proteomics & Bioinformatics
|
April 29, 2025
UNISOM: Unified Somatic Calling and Machine Learning-based Classification Enhance the Discovery of CHIP
Shulan Tian, Garrett Jenkinson, Alejandro Ferrer, et al.
European Journal of Human Genetics : EJHG
|
April 13, 2019
Variants in DOCK3 cause developmental delay and hypotonia
Kimberly Wiltrout, Alejandro Ferrer, Ingrid van de Laar, et al.
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of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
The American Journal of Surgical Pathology
|
May 3, 2021
Pathology, Radiology, and Genetics of Interstitial Lung Disease in Patients With Shortened Telomeres
Matthew J Cecchini, Tara Tarmey, Allison Ferreira, et al.
Mayo Clinic Proceedings
|
July 2, 2019
Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained Cytopenias
Abhishek A Mangaonkar, Alejandro Ferrer, Filippo Pinto E Vairo, et al.
British Journal of Haematology
|
June 23, 2020
Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients
Antoine N Saliba, Alejandro Ferrer, Naseema Gangat, et al.
Haematologica
|
July 11, 2020
A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype
Laura Schultz-Rogers, Francis P Lach, Kimberly A Rickman, et al.
Blood Cancer Journal
|
November 18, 2020
Functional validation of TERT and TERC variants of uncertain significance in patients with short telomere syndromes
Alejandro Ferrer, Abhishek A Mangaonkar, Susanna Stroik, et al.
American Journal of Hematology
|
June 15, 2026
Promoter TERT-Related Hematopoietic Somatic Mosaicism in Patients With Telomere Biology Disorders
Madeline Franke, Rachel Kirchner, Bianca Barredo, et al.
Haematologica
|
December 4, 2025
Inherited DNA repair variants are associated with clonal hematopoiesis and cardiovascular risk in men with metastatic prostate cancer
Olisaemeka Ogbue, Yael Kusne, Osama Mosalem, et al.
British Journal of Haematology
|
March 5, 2025
Prevalence of cytopenia(s) and somatic variants in patients with DDX41 mutant germline predisposition syndrome
Yael Kusne, Talha Badar, Terra Lasho, et al.
Genomics, Proteomics & Bioinformatics
|
April 29, 2025
UNISOM: Unified Somatic Calling and Machine Learning-based Classification Enhance the Discovery of CHIP
Shulan Tian, Garrett Jenkinson, Alejandro Ferrer, et al.
European Journal of Human Genetics : EJHG
|
April 13, 2019
Variants in DOCK3 cause developmental delay and hypotonia
Kimberly Wiltrout, Alejandro Ferrer, Ingrid van de Laar, et al.
Page
of 6