Raman Sood

National Institutes of Health — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

44h-index10.5kcitations155works0.42yr avg
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Research Topics

Zebrafish Biomedical Research Applications(23), CRISPR and Genetic Engineering(19), Acute Myeloid Leukemia Research(17), Epigenetics and DNA Methylation(16), RNA and protein synthesis mechanisms(10)

Publications155 total

Macrophages Mediate Mesoscale Brain Mechanical Homeostasis
Advanced Materials·2025Open Access
A single nucleotide polymorphism in the TCL1A promoter is not protective in patients with germ line RUNX1-FPD
Blood Neoplasia·2025Open Access
Metabolic rerouting of valine and isoleucine oxidation increases survival in zebrafish models of disorders of propionyl-CoA metabolism
Human Molecular Genetics·2025
The transcription factors Tfeb and Tfe3 are required for survival and embryonic development of pancreas and liver in zebrafish
PLoS Genetics·2025· 2 citedOpen Access
DNA Sequencing Technologies in Accelerating Molecular Breeding
Genetics.·2024Open Access
Organ specific microenvironmental MR1 expression in cutaneous melanoma
2023· 2 citedOpen Access
Macrophage mediated mesoscale brain mechanical homeostasis mechanically imaged via optical tweezers and Brillouin microscopy <i>in vivo</i>
2023· 3 citedOpen Access
Genomic landscape of patients with germline <i>RUNX1</i> variants and familial platelet disorder with myeloid malignancy
Blood Advances·2023· 30 citedOpen Access
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in <i>RUNX1</i>, <i>GATA2</i>, and <i>DDX41</i>
Blood Advances·2023· 36 citedOpen Access
A novel de novo <i>TP63</i> mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly
Molecular Genetics & Genomic Medicine·2023· 3 citedOpen Access
Genomic Landscape of Patients with Germline <i>RUNX1</i> Variants and Familial Platelet Disorder with Myeloid Malignancy
2023· 5 citedOpen Access
Fluorescent PCR–based Screening Methods for Precise Knock-in of Small DNA Fragments and Point Mutations in Zebrafish
BIO-PROTOCOL·2023Open Access
A robust pipeline for efficient knock-in of point mutations and epitope tags in zebrafish using fluorescent PCR based screening
BMC Genomics·2022· 14 citedOpen Access
Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in <i>RUNX1</i>, <i>GATA2</i> and <i>DDX41</i>
Blood·2022· 6 cited
Zrsr2 Is Essential for the Embryonic Development and Splicing of Minor Introns in RNA and Protein Processing Genes in Zebrafish
International Journal of Molecular Sciences·2022· 6 citedOpen Access
Dysregulated myosin in Hermansky-Pudlak syndrome lung fibroblasts is associated with increased cell motility
Respiratory Research·2022· 6 citedOpen Access
A Comprehensive Review of Indel Detection Methods for Identification of Zebrafish Knockout Mutants Generated by Genome-Editing Nucleases
Genes·2022· 9 citedOpen Access
Clonal hematopoiesis in patients with <i>ANKRD26</i> or <i>ETV6</i> germline mutations
Blood Advances·2022· 25 citedOpen Access
A Novel <i>de novo TP63</i> Mutation in Whole Exome Sequencing of a Syrian Family with Oral Cleft and Ectrodactyly
2022Open Access
Clonal hematopoiesis in individuals with <i>ANKRD26</i> or <i>ETV6</i> germline mutations
2021Open Access
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Frequent Co-authors

Blake Carrington(12), Kevin Bishop(11), Jeffrey M. Trent(10), Shawn M. Burgess(8), Paul Liu(8), John D. Carpten(7), Christiane M. Robbins(7), Joan E. Bailey‐Wilson(7), Elizabeth M. Gillanders(7), MaryPat Jones(7), Gaurav K. Varshney(6), Izabela Makałowska(6), Diana Freas‐Lutz(5), Milton A. English(5), Settara C. Chandrasekharappa(5), Wuhong Pei(4), James C. Mullikin(4), Daniel L. Kastner(4), Sarah D. Isaacs(4), Charles M. Ewing(4)