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The Journal of Experimental Medicine
|
April 15, 2021
Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript
Lara Wahlster, Jeffrey M Verboon, Leif S Ludwig, et al.
Nature Biotechnology
|
August 14, 2020
Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling
Caleb A Lareau, Leif S Ludwig, Christoph Muus, et al.
The Journal of Experimental Medicine
|
March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutation
Nour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Journal of Clinical Immunology
|
April 19, 2020
Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction
Jeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, et al.
Nature Genetics
|
June 29, 2023
Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells
Caleb A Lareau, Sonia M Dubois, Frank A Buquicchio, et al.
Blood
|
January 14, 2022
Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1
Leif S Ludwig, Caleb A Lareau, Erik L Bao, et al.
Nature Communications
|
August 18, 2023
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Parsa Akbari, Dragana Vuckovic, Luca Stefanucci, et al.
Nature
|
November 8, 2023
Latent human herpesvirus 6 is reactivated in CAR T cells
Caleb A Lareau, Yajie Yin, Katie Maurer, et al.
American Journal of Human Genetics
|
December 4, 2018
The Genetic Landscape of Diamond-Blackfan Anemia
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
Monica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
The Journal of Experimental Medicine
|
April 15, 2021
Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript
Lara Wahlster, Jeffrey M Verboon, Leif S Ludwig, et al.
Nature Biotechnology
|
August 14, 2020
Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling
Caleb A Lareau, Leif S Ludwig, Christoph Muus, et al.
The Journal of Experimental Medicine
|
March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutation
Nour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Journal of Clinical Immunology
|
April 19, 2020
Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction
Jeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, et al.
Nature Genetics
|
June 29, 2023
Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells
Caleb A Lareau, Sonia M Dubois, Frank A Buquicchio, et al.
Blood
|
January 14, 2022
Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1
Leif S Ludwig, Caleb A Lareau, Erik L Bao, et al.
Nature Communications
|
August 18, 2023
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Parsa Akbari, Dragana Vuckovic, Luca Stefanucci, et al.
Nature
|
November 8, 2023
Latent human herpesvirus 6 is reactivated in CAR T cells
Caleb A Lareau, Yajie Yin, Katie Maurer, et al.
American Journal of Human Genetics
|
December 4, 2018
The Genetic Landscape of Diamond-Blackfan Anemia
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 8, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
Monica H Wojcik, Gabrielle Lemire, Maha S Zaki, et al.
Page
of 4