Author details

Full Name

Vijay G Sankaran

Affiliation

ORCID

Career Start Year

2000

Papers

156

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36463683	Development of a Thalassemia International Prognostic Scoring System (TIPSS).	Blood Cells, Molecules, and Diseases	2023
36306384	CD11c regulates neutrophil maturation.	Blood advances	2023
37596262	A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.	Nat Commun	2023
37586368	RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.	Dev Cell	2023
37653227	Author Correction: Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling.	Nat Biotechnol	2023
37558590	Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19.	Blood Cells Mol Dis	2023
37407873	MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development.		2023
37155167	Perspectives of Rare Disease Experts on Newborn Genome Sequencing.	JAMA Netw Open	2023
36907615	Thalassemia.		2023
36907604	Fetal Hemoglobin Regulation in Beta-Thalassemia.	Hematol Oncol Clin North Am	2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
36826849	Hacking hematopoiesis - emerging tools for examining variant effects.		2023
37137305	Massively parallel base editing to map variant effects in human hematopoiesis.	Cell	2023
36945604	RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.	medRxiv	2023
37386249	Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells.	Nat Genet	2023
37067177	Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM-associated syndromes.	Am J Med Genet A	2023
36803603	Human hematopoietic stem cell vulnerability to ferroptosis.	Cell	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36993312	Genetic regulation of fetal hemoglobin across global populations.	medRxiv	2023
36792778	Mitochondrial single-cell ATAC-seq for high-throughput multi-omic detection of mitochondrial genotypes and chromatin accessibility.	Nat Protoc	2023
36736573	Exploiting somatic mutations to decipher human blood production: a natural lineage-tracing strategy.		2023
35138379	Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.	Hum Mol Genet	2022
35969771	Inferring gene regulation from stochastic transcriptional variation across single cells at steady state.	Proc Natl Acad Sci U S A	2022
36227997	Cellular barcoding to decipher clonal dynamics in disease.	Science	2022
35373283	Patchwork Cancer Predisposition.	Cancer Discovery	2022
36138230	Multi-omics on our multitudes.	Nature Genetics	2022
36332568	Vade-MECOM: How to peel back the layers of hematopoiesis.		2022
35668323	Variant to function mapping at single-cell resolution through network propagation.	Nat Biotechnol	2022
36513657	Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.	Nat Commun	2022
34990411	Clonal hematopoiesis in sickle cell disease.	J Clin Invest	2022
35298850	A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome.	British Journal of Haematology	2022
34862982	Risk of mortality from anemia and iron overload in nontransfusion-dependent Î²-thalassemia.	American Journal of Hematology	2022
35030251	Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1.	Blood	2022
35210612	Mitochondrial variant enrichment from high-throughput single-cell RNA sequencing resolves clonal populations.	Nat Biotechnol	2022
35118467	Variant to function mapping at single-cell resolution through network propagation.	bioRxiv	2022
35013207	Functional dissection of inherited non-coding variation influencing multiple myeloma risk.	Nat Commun	2022
35007327	Genome-wide association study on 13â¿¿167 individuals identifies regulators of blood CD34+cell levels.	Blood	2022
34758059	Germline GATA1s-generating mutations predispose toÂ leukemia with acquired trisomy 21 and Down syndrome-like phenotype.	Blood	2022
34697800	Primary HBB gene mutation severity and long-term outcomes in a global cohort of Î²-thalassaemia.	British Journal of Haematology	2022
34936695	Molecular and cellular mechanisms that regulate human erythropoiesis.	Blood	2022
35262092	Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19.	medRxiv	2022
34404810	A unified model of human hemoglobin switching through single-cell genome editing.	Nat Commun	2021
33857290	Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript.	J Exp Med	2021
33901135	Deciphering transcriptional and functional heterogeneity in hematopoiesis with single-cell genomics.	Current Opinion in Hematology	2021
34112698	Longitudinal Single-Cell Dynamics of Chromatin Accessibility and Mitochondrial Mutations in Chronic Lymphocytic Leukemia Mirror Disease History.	Cancer Discov	2021
33521754	Long-Term Patient-Customized Therapy for a Pathogenic Mutation.	Med	2021
33882642	Survival and causes of death in 2,033 patients with non-transfusion-dependent Î²-thalassemia	Haematologica	2021
33978700	I SPI1 something needed for B cells.	Journal of Experimental Medicine	2021
34244724	CUT&RUNTools 2.0: a pipeline for single-cell and bulk-level CUT&RUN and CUT&Tag data analysis.	Bioinformatics	2021
34083792	Scalable, multimodal profiling of chromatin accessibility, gene expression and protein levels in single cells.	Nat Biotechnol	2021