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American Journal of Medical Genetics. Part A
|
February 23, 2023
Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance
Elaine M Fan, Jennie Vagher, Jessica A Meznarich, et al.
Clinical Genetics
|
May 31, 2026
A Proposed Clinical Diagnostic Framework for Short Telomere Syndrome
Andrew Courtwright, Richard A King, Jennie Vagher, et al.
Leukemia
|
October 21, 2021
AML with germline DDX41 variants is a clinicopathologically distinct entity with an indolent clinical course and favorable outcome
Peng Li, Thomas White, Wei Xie, et al.
JCO Precision Oncology
|
June 20, 2025
Hematologic Malignancy Frequency, Phenotypes, and Outcomes in Li-Fraumeni Syndrome
Jennie Vagher, Anna Zakas, Lauren Donovan, et al.
Blood
|
June 7, 2022
The genetic landscape of germline DDX41 variants predisposing to myeloid neoplasms
Peng Li, Sara Brown, Margaret Williams, et al.
Blood Advances
|
March 3, 2025
Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing
Ting Wen, Steven E Boyden, Caleb M Hocutt, et al.
Molecular Cancer Research : MCR
|
May 18, 2026
Variation at the R181 residue of p53 confers loss of p53 DNA binding cooperativity with the retention of mitochondrial-associated apoptosis
Renyta Moses, Alexandra Indeglia, Alison S Levine, et al.
Leukemia
|
May 7, 2025
Predisposition to hematopoietic malignancies by deleterious germline CHEK2 variants
Ryan J Stubbins, Stephen Arnovitz, Jennie Vagher, et al.
Biorxiv : the Preprint Server for Biology
|
August 20, 2025
Variation at the R181 residue of p53 confers loss of p53 DNA binding cooperativity with the retention of mitochondrial-associated apoptosis
Renyta Moses, Alexandra Indeglia, Alison S Levine, et al.
Familial Cancer
|
August 11, 2025
Parental perspectives on the use of tumor molecular profiling and germline genetic testing during their children's cancer treatment
Marcelo M Sleiman, Muriel R Statman, Mary Rose Yockel, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics. Part A
|
February 23, 2023
Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance
Elaine M Fan, Jennie Vagher, Jessica A Meznarich, et al.
Clinical Genetics
|
May 31, 2026
A Proposed Clinical Diagnostic Framework for Short Telomere Syndrome
Andrew Courtwright, Richard A King, Jennie Vagher, et al.
Leukemia
|
October 21, 2021
AML with germline DDX41 variants is a clinicopathologically distinct entity with an indolent clinical course and favorable outcome
Peng Li, Thomas White, Wei Xie, et al.
JCO Precision Oncology
|
June 20, 2025
Hematologic Malignancy Frequency, Phenotypes, and Outcomes in Li-Fraumeni Syndrome
Jennie Vagher, Anna Zakas, Lauren Donovan, et al.
Blood
|
June 7, 2022
The genetic landscape of germline DDX41 variants predisposing to myeloid neoplasms
Peng Li, Sara Brown, Margaret Williams, et al.
Blood Advances
|
March 3, 2025
Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing
Ting Wen, Steven E Boyden, Caleb M Hocutt, et al.
Molecular Cancer Research : MCR
|
May 18, 2026
Variation at the R181 residue of p53 confers loss of p53 DNA binding cooperativity with the retention of mitochondrial-associated apoptosis
Renyta Moses, Alexandra Indeglia, Alison S Levine, et al.
Leukemia
|
May 7, 2025
Predisposition to hematopoietic malignancies by deleterious germline CHEK2 variants
Ryan J Stubbins, Stephen Arnovitz, Jennie Vagher, et al.
Biorxiv : the Preprint Server for Biology
|
August 20, 2025
Variation at the R181 residue of p53 confers loss of p53 DNA binding cooperativity with the retention of mitochondrial-associated apoptosis
Renyta Moses, Alexandra Indeglia, Alison S Levine, et al.
Familial Cancer
|
August 11, 2025
Parental perspectives on the use of tumor molecular profiling and germline genetic testing during their children's cancer treatment
Marcelo M Sleiman, Muriel R Statman, Mary Rose Yockel, et al.
Page
of 3