| Year |
Citation |
Score |
| 2024 |
Zhao J, Cato LD, Arora UP, Bao EL, Bryant SC, Williams N, Jia Y, Goldman SR, Nangalia J, Erb MA, Vos SM, Armstrong SA, Sankaran VG. Inherited blood cancer predisposition through altered transcription elongation. Cell. PMID 38218188 DOI: 10.1016/j.cell.2023.12.016 |
0.32 |
|
| 2023 |
Akbari P, Vuckovic D, Stefanucci L, Jiang T, Kundu K, Kreuzhuber R, Bao EL, Collins JH, Downes K, Grassi L, Guerrero JA, Kaptoge S, Knight JC, Meacham S, Sambrook J, ... ... Sankaran VG, et al. A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Nature Communications. 14: 5023. PMID 37596262 DOI: 10.1038/s41467-023-40679-y |
0.311 |
|
| 2023 |
Martin-Rufino JD, Castano N, Pang M, Grody EI, Joubran S, Caulier A, Wahlster L, Li T, Qiu X, Riera-Escandell AM, Newby GA, Al'Khafaji A, Chaudhary S, Black S, Weng C, ... ... Sankaran VG, et al. Massively parallel base editing to map variant effects in human hematopoiesis. Cell. PMID 37137305 DOI: 10.1016/j.cell.2023.03.035 |
0.345 |
|
| 2023 |
Cato LD, Li R, Lu HY, Yu F, Wissman M, Mkumbe BS, Ekwattanakit S, Deelen P, Mwita L, Sangeda RZ, Suksangpleng T, Riolueang S, Bronson PG, Paul DS, Kawabata E, ... ... Sankaran VG, et al. Genetic regulation of fetal hemoglobin across global populations. Medrxiv : the Preprint Server For Health Sciences. PMID 36993312 DOI: 10.1101/2023.03.24.23287659 |
0.338 |
|
| 2023 |
Lu HY, Orkin SH, Sankaran VG. Fetal Hemoglobin Regulation in Beta-Thalassemia. Hematology/Oncology Clinics of North America. 37: 301-312. PMID 36907604 DOI: 10.1016/j.hoc.2022.12.002 |
0.458 |
|
| 2023 |
Gundry M, Sankaran VG. Hacking hematopoiesis - emerging tools for examining variant effects. Disease Models & Mechanisms. 16. PMID 36826849 DOI: 10.1242/dmm.049857 |
0.317 |
|
| 2022 |
Voit RA, Tao L, Yu F, Cato LD, Cohen B, Fleming TJ, Antoszewski M, Liao X, Fiorini C, Nandakumar SK, Wahlster L, Teichert K, Regev A, Sankaran VG. A genetic disorder reveals a hematopoietic stem cell regulatory network co-opted in leukemia. Nature Immunology. 24: 69-83. PMID 36522544 DOI: 10.1038/s41590-022-01370-4 |
0.304 |
|
| 2022 |
Sankaran VG, Weissman JS, Zon LI. Cellular barcoding to decipher clonal dynamics in disease. Science (New York, N.Y.). 378: eabm5874. PMID 36227997 DOI: 10.1126/science.abm5874 |
0.448 |
|
| 2022 |
Yu F, Cato LD, Weng C, Liggett LA, Jeon S, Xu K, Chiang CWK, Wiemels JL, Weissman JS, de Smith AJ, Sankaran VG. Variant to function mapping at single-cell resolution through network propagation. Biorxiv : the Preprint Server For Biology. PMID 35118467 DOI: 10.1101/2022.01.23.477426 |
0.301 |
|
| 2022 |
Ludwig L, Lareau CA, Bao EL, Liu N, Utsugisawa T, Tseng AM, Myers SA, Verboon JM, Ulirsch JC, Luo W, Muus C, Fiorini C, Olive ME, Vockley CM, Munschauer M, ... ... Sankaran VG, et al. A Congenital Anemia Reveals Distinct Targeting Mechanisms for Master Transcription Factor GATA1. Blood. PMID 35030251 DOI: 10.1182/blood.2021013753 |
0.484 |
|
| 2021 |
Caulier AL, Sankaran VG. Molecular and cellular mechanisms that regulate human erythropoiesis. Blood. PMID 34936695 DOI: 10.1182/blood.2021011044 |
0.313 |
|
| 2021 |
Shen Y, Li R, Teichert K, Montbleau KE, Verboon JM, Voit RA, Sankaran VG. Pathogenic BCL11A variants provide insights into the mechanisms of human fetal hemoglobin silencing. Plos Genetics. 17: e1009835. PMID 34634037 DOI: 10.1371/journal.pgen.1009835 |
0.311 |
|
| 2021 |
Shen Y, Verboon JM, Zhang Y, Liu N, Kim YJ, Marglous S, Nandakumar SK, Voit RA, Fiorini C, Ejaz A, Basak A, Orkin SH, Xu J, Sankaran VG. A unified model of human hemoglobin switching through single-cell genome editing. Nature Communications. 12: 4991. PMID 34404810 DOI: 10.1038/s41467-021-25298-9 |
0.525 |
|
| 2020 |
Taylor AM, Macari ER, Chan IT, Blair MC, Doulatov S, Vo LT, Raiser DM, Siva K, Basak A, Pirouz M, Shah AN, McGrath K, Humphries JM, Stillman E, Alter BP, ... ... Sankaran VG, et al. Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia. Science Translational Medicine. 12. PMID 33087503 DOI: 10.1126/scitranslmed.abb5831 |
0.453 |
|
| 2020 |
Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Lin AE, ... ... Sankaran VG, et al. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. PMID 33057201 DOI: 10.1038/s41586-020-2819-2 |
0.31 |
|
| 2020 |
Liggett LA, Sankaran VG. Unraveling Hematopoiesis through the Lens of Genomics. Cell. 182: 1384-1400. PMID 32946781 DOI: 10.1016/J.Cell.2020.08.030 |
0.36 |
|
| 2020 |
Vuckovic D, Bao EL, Akbari P, Lareau CA, Mousas A, Jiang T, Chen MH, Raffield LM, Tardaguila M, Huffman JE, Ritchie SC, Megy K, Ponstingl H, Penkett CJ, Albers PK, ... ... Sankaran VG, et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 182: 1214-1231.e11. PMID 32888494 DOI: 10.1016/J.Cell.2020.08.008 |
0.428 |
|
| 2020 |
Chen MH, Raffield LM, Mousas A, Sakaue S, Huffman JE, Moscati A, Trivedi B, Jiang T, Akbari P, Vuckovic D, Bao EL, Zhong X, Manansala R, Laplante V, Chen M, ... ... Sankaran VG, et al. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Cell. 182: 1198-1213.e14. PMID 32888493 DOI: 10.1016/J.Cell.2020.06.045 |
0.331 |
|
| 2020 |
Lareau CA, Ludwig LS, Muus C, Gohil SH, Zhao T, Chiang Z, Pelka K, Verboon JM, Luo W, Christian E, Rosebrock D, Getz G, Boland GM, Chen F, Buenrostro JD, ... ... Sankaran VG, et al. Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling. Nature Biotechnology. PMID 32788668 DOI: 10.1038/S41587-020-0645-6 |
0.36 |
|
| 2020 |
Liggett LA, Voit RA, Sankaran VG. Sowing the Seeds of Clonal Hematopoiesis. Cell Stem Cell. 27: 195-197. PMID 32763180 DOI: 10.1016/J.Stem.2020.07.011 |
0.362 |
|
| 2020 |
Nandakumar SK, Liao X, Sankaran VG. In The Blood: Connecting Variant to Function In Human Hematopoiesis. Trends in Genetics : Tig. PMID 32534791 DOI: 10.1016/J.Tig.2020.05.006 |
0.419 |
|
| 2020 |
Verboon JM, Mahmut D, Kim AR, Nakamura M, Abdulhay NJ, Nandakumar SK, Gupta N, Akie TE, Geddis AE, Manes B, Kapp ME, Hofmann I, Gabriel SB, Klein DE, Williams DA, ... ... Sankaran VG, et al. Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction. Journal of Clinical Immunology. PMID 32303876 DOI: 10.1007/S10875-020-00778-7 |
0.431 |
|
| 2020 |
Gianferante DM, Wlodarski MW, Atsidaftos E, Da Costa L, Delaporta P, Farrar JE, Goldman FD, Hussain M, Kattamis A, Leblanc T, Lipton JM, Niemeyer CM, Pospisilova D, Quarello P, Ramenghi U, ... Sankaran VG, et al. Genotype-phenotype association and variant characterization in Diamond-Blackfan anemia caused by pathogenic variants in RPL35A. Haematologica. PMID 32241839 DOI: 10.3324/Haematol.2020.246629 |
0.363 |
|
| 2020 |
Basak A, Munschauer M, Lareau CA, Montbleau KE, Ulirsch JC, Hartigan CR, Schenone M, Lian J, Wang Y, Huang Y, Wu X, Gehrke L, Rice CM, An X, Christou HA, ... ... Sankaran VG, et al. Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation. Nature Genetics. PMID 31959994 DOI: 10.1038/S41588-019-0568-7 |
0.548 |
|
| 2019 |
Lareau CA, Ludwig LS, Sankaran VG. Longitudinal assessment of clonal mosaicism in human hematopoiesis via mitochondrial mutation tracking. Blood Advances. 3: 4161-4165. PMID 31841597 DOI: 10.1182/Bloodadvances.2019001196 |
0.377 |
|
| 2019 |
Justice MJ, Hmeljak J, Sankaran VG, Socolovsky M, Zon LI. From blood development to disease: a paradigm for clinical translation. Disease Models & Mechanisms. PMID 31836582 DOI: 10.1242/Dmm.043661 |
0.468 |
|
| 2019 |
Bao EL, Cheng AN, Sankaran VG. The genetics of human hematopoiesis and its disruption in disease. Embo Molecular Medicine. e10316. PMID 31313878 DOI: 10.15252/Emmm.201910316 |
0.453 |
|
| 2019 |
Cheng AN, Bao EL, Fiorini C, Sankaran VG. Macrothrombocytopenia associated with a rare GFI1B missense variant confounding the presentation of immune thrombocytopenia. Pediatric Blood & Cancer. e27874. PMID 31207059 DOI: 10.1002/Pbc.27874 |
0.365 |
|
| 2019 |
Ludwig LS, Lareau CA, Bao EL, Nandakumar SK, Muus C, Ulirsch JC, Chowdhary K, Buenrostro JD, Mohandas N, An X, Aryee MJ, Regev A, Sankaran VG. Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis. Cell Reports. 27: 3228-3240.e7. PMID 31189107 DOI: 10.1016/J.Celrep.2019.05.046 |
0.438 |
|
| 2019 |
Sankaran VG. A chance encounter changes everything. Nature Medicine. PMID 31171867 DOI: 10.1038/S41591-019-0418-2 |
0.328 |
|
| 2019 |
Nandakumar SK, McFarland SK, Mateyka LM, Lareau CA, Ulirsch JC, Ludwig LS, Agarwal G, Engreitz JM, Przychodzen B, McConkey M, Cowley GS, Doench JG, Maciejewski JP, Ebert BL, Root DE, ... Sankaran VG, et al. Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis. Elife. 8. PMID 31070582 DOI: 10.7554/Elife.44080 |
0.439 |
|
| 2019 |
Zhang S, Macias-Garcia A, Ulirsch JC, Velazquez J, Butty VL, Levine SS, Sankaran VG, Chen JJ. HRI coordinates translation necessary for protein homeostasis and mitochondrial function in erythropoiesis. Elife. 8. PMID 31033440 DOI: 10.7554/Elife.46976 |
0.3 |
|
| 2019 |
Abdulhay NJ, Fiorini C, Verboon JM, Ludwig LS, Ulirsch JC, Zieger B, Lareau CA, Mi X, Roy A, Obeng EA, Erlacher M, Gupta N, Gabriel SB, Ebert BL, Niemeyer CM, ... ... Sankaran VG, et al. Impaired human hematopoiesis due to a cryptic intronic splicing mutation. The Journal of Experimental Medicine. PMID 30914438 DOI: 10.1084/Jem.20181625 |
0.406 |
|
| 2019 |
Liang L, Peng Y, Zhang J, Zhang Y, Roy M, Han X, Xiao X, Sun S, Liu H, Nie L, Kuang Y, Zhu Z, Deng J, Xia Y, Sankaran VG, et al. Deubiquitylase USP7 regulates human terminal erythroid differentiation by stabilizing GATA1. Haematologica. PMID 30872372 DOI: 10.3324/Haematol.2018.206227 |
0.367 |
|
| 2019 |
Ulirsch JC, Lareau CA, Bao EL, Ludwig LS, Guo MH, Benner C, Satpathy AT, Kartha VK, Salem RM, Hirschhorn JN, Finucane HK, Aryee MJ, Buenrostro JD, Sankaran VG. Interrogation of human hematopoiesis at single-cell and single-variant resolution. Nature Genetics. PMID 30858613 DOI: 10.1038/S41588-019-0362-6 |
0.438 |
|
| 2019 |
Ludwig LS, Lareau CA, Ulirsch JC, Christian E, Muus C, Li LH, Pelka K, Ge W, Oren Y, Brack A, Law T, Rodman C, Chen JH, Boland GM, Hacohen N, ... ... Sankaran VG, et al. Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell Genomics. Cell. PMID 30827679 DOI: 10.1016/J.Cell.2019.01.022 |
0.41 |
|
| 2019 |
Bao EL, Lareau CA, Brugnara C, Fulcher I, Barau C, Moutereau S, Habibi A, Badaoui B, Berkenou J, Bartolucci P, Galactéros F, Platt OS, Mahaney M, Sankaran VG. Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort. American Journal of Hematology. PMID 30680775 DOI: 10.1002/Ajh.25421 |
0.369 |
|
| 2019 |
Nandakumar SK, McFarland SK, Mateyka LM, Lareau CA, Ulirsch JC, Ludwig LS, Agarwal G, Engreitz JM, Przychodzen B, McConkey M, Cowley GS, Doench JG, Maciejewski JP, Ebert BL, Root DE, ... Sankaran VG, et al. Author response: Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis Elife. DOI: 10.7554/Elife.44080.041 |
0.381 |
|
| 2018 |
Ulirsch JC, Verboon JM, Kazerounian S, Guo MH, Yuan D, Ludwig LS, Handsaker RE, Abdulhay NJ, Fiorini C, Genovese G, Lim ET, Cheng A, Cummings BB, Chao KR, Beggs AH, ... ... Sankaran VG, et al. The Genetic Landscape of Diamond-Blackfan Anemia. American Journal of Human Genetics. PMID 30503522 DOI: 10.1016/J.Ajhg.2018.10.027 |
0.382 |
|
| 2018 |
Montbleau KE, Sankaran VG. A chance to cut (the genome) is a chance to cure. Blood. 131: 1884-1885. PMID 29699995 DOI: 10.1182/Blood-2018-03-839787 |
0.327 |
|
| 2018 |
Khajuria RK, Munschauer M, Ulirsch JC, Fiorini C, Ludwig LS, McFarland SK, Abdulhay NJ, Specht H, Keshishian H, Mani DR, Jovanovic M, Ellis SR, Fulco CP, Engreitz JM, Schütz S, ... ... Sankaran VG, et al. Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis. Cell. PMID 29551269 DOI: 10.1016/J.Cell.2018.02.036 |
0.45 |
|
| 2018 |
Chennupati V, Veiga DF, Maslowski KM, Andina N, Tardivel A, Yu EC, Stilinovic M, Simillion C, Duchosal MA, Quadroni M, Roberts I, Sankaran VG, MacDonald HR, Fasel N, Angelillo-Scherrer A, et al. Ribonuclease inhibitor 1 regulates erythropoiesis by controlling GATA1 mRNA translation. The Journal of Clinical Investigation. PMID 29408805 DOI: 10.1172/Jci94956 |
0.392 |
|
| 2018 |
Choudhuri A, Trompouki E, Abraham BJ, Colli L, Mallard W, Yang M, Vinjamur D, Ghamari A, Nandakumar S, Hoi K, Hummel B, Boatman S, Chan V, Bowman TV, Yang S, ... ... Sankaran VG, et al. Transcriptional Signaling Centers Govern Human Erythropoiesis and Harbor Genetic Variations of Red Blood Cell Traits Blood. 132: 1277-1277. DOI: 10.1182/Blood-2018-99-118637 |
0.552 |
|
| 2018 |
Basak A, Munschauer M, Ulirsch JC, Montbleau KE, Hartigan CR, Schenone M, Lian J, Wang Y, Huang Y, Wu X, Gehrke L, Rice CM, An X, Christou HA, Narla M, ... ... Sankaran VG, et al. Control of Human Hemoglobin Switching By LIN28B-Mediated Regulation of BCL11A Translation Blood. 132: 412-412. DOI: 10.1182/Blood-2018-99-117440 |
0.574 |
|
| 2018 |
Giri N, Gianferante M, Atsidaftos E, Wlodarski MW, Quarello P, Volejnikova J, Delaporta P, Sankaran VG, Farrar JE, Hussain M, McReynolds LJ, Kattamis A, Lipton JM, Niemeyer C, Pospisilova D, et al. Phenotypes of Diamond Blackfan Anemia Patients with RPL35A Haploinsufficiency Due to 3q29 Deletion Compared with RPL35A Single Nucleotide Variants or Small Insertion/Deletions Blood. 132: 3854-3854. DOI: 10.1182/Blood-2018-99-117171 |
0.324 |
|
| 2018 |
Bao EL, Ulirsch JC, Lareau CA, Ludwig LS, Guo MH, Benner C, Satpathy AT, Kartha VK, Salem RM, Hirschhorn JN, Finucane HK, Aryee MJ, Buenrostro JD, Sankaran VG. Dissecting the Regulation of Human Hematopoiesis at Single-Cell and Single-Variant Resolution Blood. 132: 531-531. DOI: 10.1182/Blood-2018-99-112624 |
0.456 |
|
| 2018 |
Abdulhay N, Verboon J, Ulirsch J, Zieger B, Mi X, Obeng E, Erlacher M, Gupta N, Gabriel S, Ebert B, Niemeyer C, Khoriaty R, Ancliff P, Gazda H, Wlodarski M, ... Sankaran V, et al. A Cryptic Intronic GATA1 Splicing Mutation Provides Insights Into Human Hematopoietic Differentiation Experimental Hematology. 64: S53. DOI: 10.1016/J.Exphem.2018.06.185 |
0.353 |
|
| 2017 |
Kim AR, Sankaran VG. Thrombopoietin: tickling the HSC's fancy. Embo Molecular Medicine. PMID 29191946 DOI: 10.15252/Emmm.201708450 |
0.407 |
|
| 2017 |
Fiorini C, Abdulhay NJ, McFarland SK, Munschauer M, Ulirsch JC, Chiarle R, Sankaran VG. Developmentally-Faithful and Effective Human Erythropoiesis in Immunodeficient and Kit Mutant Mice. American Journal of Hematology. PMID 28568895 DOI: 10.1002/Ajh.24805 |
0.393 |
|
| 2017 |
Kim AR, Ulirsch JC, Wilmes S, Unal E, Moraga I, Karakukcu M, Yuan D, Kazerounian S, Abdulhay NJ, King DS, Gupta N, Gabriel SB, Lander ES, Patiroglu T, Ozcan A, ... ... Sankaran VG, et al. Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation. Cell. 168: 1053-1064.e15. PMID 28283061 DOI: 10.1016/J.Cell.2017.02.026 |
0.314 |
|
| 2016 |
Guo MH, Nandakumar SK, Ulirsch JC, Zekavat SM, Buenrostro JD, Natarajan P, Salem RM, Chiarle R, Mitt M, Kals M, Pärn K, Fischer K, Milani L, Mägi R, Palta P, ... ... Sankaran VG, et al. Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Proceedings of the National Academy of Sciences of the United States of America. PMID 28031487 DOI: 10.1073/Pnas.1619052114 |
0.432 |
|
| 2016 |
Han X, Zhang J, Peng Y, Peng M, Chen X, Chen H, Song J, Hu X, Ye M, Li J, Sankaran VG, Hillyer CD, Mohandas N, An X, Liu J. Unexpected role for p19INK4d in post-transcriptional regulation of GATA1 and modulation of human terminal erythropoiesis. Blood. PMID 27879259 DOI: 10.1182/Blood-2016-09-739268 |
0.33 |
|
| 2016 |
Ludwig LS, Khajuria RK, Sankaran VG. Emerging cellular and gene therapies for congenital anemias. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 27792859 DOI: 10.1002/Ajmg.C.31529 |
0.402 |
|
| 2016 |
Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen MH, Auer PL, Floyd JS, Huang J, Lange L, van Rooij FJ, Gibbs RA, Metcalf G, Muzny D, ... ... Sankaran VG, et al. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 785. PMID 27588453 DOI: 10.1016/J.Ajhg.2016.08.002 |
0.406 |
|
| 2016 |
Abdulhay N, Fiorini C, Kumánovics A, Sun AA, Hansen-Rejali J, Voelkerding KV, Rosenzweig SD, Hill HR, Sankaran VG. Normal hematologic parameters and fetal hemoglobin silencing with heterozygous IKZF1 mutations. Blood. PMID 27581358 DOI: 10.1182/Blood-2016-08-731943 |
0.395 |
|
| 2016 |
Fukuda Y, Cheong PL, Lynch J, Brighton C, Frase S, Kargas V, Rampersaud E, Wang Y, Sankaran VG, Yu B, Ney PA, Weiss MJ, Vogel P, Bond PJ, Ford RC, et al. The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6. Nature Communications. 7: 12353. PMID 27507172 DOI: 10.1038/Ncomms12353 |
0.392 |
|
| 2016 |
Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen MH, Auer PL, Floyd JS, Huang J, Lange L, van Rooij FJ, Gibbs RA, Metcalf G, Muzny D, ... ... Sankaran VG, et al. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 481-488. PMID 27486782 DOI: 10.1016/J.Ajhg.2016.06.016 |
0.422 |
|
| 2016 |
Liddicoat BJ, Hartner JC, Piskol R, Ramaswami G, Chalk AM, Kingsley PD, Sankaran VG, Wall M, Purton LE, Seeburg PH, Palis J, Orkin SH, Lu J, Li JB, Walkley CR. Adenosine-to-insoine RNA editing by ADAR1 is essential for normal murine erythropoiesis. Experimental Hematology. PMID 27373493 DOI: 10.1016/J.Exphem.2016.06.250 |
0.477 |
|
| 2016 |
Kim AR, Sankaran VG. Development of autologous blood cell therapies. Experimental Hematology. PMID 27345108 DOI: 10.1016/J.Exphem.2016.06.005 |
0.359 |
|
| 2016 |
Capellera-Garcia S, Pulecio J, Dhulipala K, Siva K, Rayon-Estrada V, Singbrant S, Sommarin MN, Walkley CR, Soneji S, Karlsson G, Raya Á, Sankaran VG, Flygare J. Defining the Minimal Factors Required for Erythropoiesis through Direct Lineage Conversion. Cell Reports. PMID 27264182 DOI: 10.1016/J.Exphem.2016.06.075 |
0.403 |
|
| 2016 |
Ulirsch JC, Nandakumar SK, Wang L, Giani FC, Zhang X, Rogov P, Melnikov A, McDonel P, Do R, Mikkelsen TS, Sankaran VG. Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits. Cell. 165: 1530-1545. PMID 27259154 DOI: 10.1016/J.Cell.2016.04.048 |
0.439 |
|
| 2016 |
Wakabayashi A, Ulirsch JC, Ludwig LS, Fiorini C, Yasuda M, Choudhuri A, McDonel P, Zon LI, Sankaran VG. Insight into GATA1 transcriptional activity through interrogation of cis elements disrupted in human erythroid disorders. Proceedings of the National Academy of Sciences of the United States of America. PMID 27044088 DOI: 10.1073/Pnas.1521754113 |
0.549 |
|
| 2016 |
Basak A, Sankaran VG. Regulation of the fetal hemoglobin silencing factor BCL11A. Annals of the New York Academy of Sciences. PMID 26963603 DOI: 10.1111/Nyas.13024 |
0.453 |
|
| 2016 |
Nandakumar SK, Ulirsch JC, Sankaran VG. Advances in understanding erythropoiesis: evolving perspectives. British Journal of Haematology. PMID 26846448 DOI: 10.1111/Bjh.13938 |
0.445 |
|
| 2016 |
Kim AR, Ulirsch JC, Wilmes S, Unal E, Moraga I, Karakukcu M, Yuan D, Kazerounian S, Gupta N, Gabriel SB, Lander ES, Patiroglu T, Ozcan A, Ozdemir M, Garcia C, ... ... Sankaran VG, et al. Discovery of the First Pathogenic Human EPO Mutation Provides Mechanistic Insight into Cytokine Signaling Blood. 128: 331-331. DOI: 10.1182/Blood.V128.22.331.331 |
0.38 |
|
| 2016 |
Sankaran VG. Hematopoiesis in natura: insight from studies of blood production in humans Experimental Hematology. 44: S36. DOI: 10.1016/J.Exphem.2016.06.034 |
0.318 |
|
| 2015 |
Giani FC, Fiorini C, Wakabayashi A, Ludwig LS, Salem RM, Jobaliya CD, Regan SN, Ulirsch JC, Liang G, Steinberg-Shemer O, Guo MH, Esko T, Tong W, Brugnara C, Hirschhorn JN, ... ... Sankaran VG, et al. Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells. Cell Stem Cell. PMID 26607381 DOI: 10.1016/J.Stem.2015.09.015 |
0.558 |
|
| 2015 |
Wakabayashi A, Sankaran VG. Society for Pediatric Research 2015 Young Investigator Award: Genetics of human hematopoiesis-What patients can teach us about blood cell production. Pediatric Research. PMID 26575596 DOI: 10.1038/Pr.2015.245 |
0.42 |
|
| 2015 |
Noh JY, Gandre-Babbe S, Wang Y, Hayes V, Yao Y, Gadue P, Sullivan SK, Chou ST, Machlus KR, Italiano JE, Kyba M, Finkelstein D, Ulirsch JC, Sankaran VG, French DL, et al. Inducible Gata1 suppression expands megakaryocyte-erythroid progenitors from embryonic stem cells. The Journal of Clinical Investigation. 125: 2369-74. PMID 25961454 DOI: 10.1172/Jci77670 |
0.403 |
|
| 2015 |
Basak A, Hancarova M, Ulirsch JC, Balci TB, Trkova M, Pelisek M, Vlckova M, Muzikova K, Cermak J, Trka J, Dyment DA, Orkin SH, Daly MJ, Sedlacek Z, Sankaran VG. BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations. The Journal of Clinical Investigation. 125: 2363-8. PMID 25938782 DOI: 10.1172/Jci81163 |
0.561 |
|
| 2015 |
Sankaran VG, Weiss MJ. Anemia: progress in molecular mechanisms and therapies. Nature Medicine. 21: 221-30. PMID 25742458 DOI: 10.1038/Nm.3814 |
0.3 |
|
| 2015 |
Sankaran VG, Ulirsch JC, Tchaikovskii V, Ludwig LS, Wakabayashi A, Kadirvel S, Lindsley RC, Bejar R, Shi J, Lovitch SB, Bishop DF, Steensma DP. X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation. The Journal of Clinical Investigation. 125: 1665-9. PMID 25705881 DOI: 10.1172/Jci78619 |
0.334 |
|
| 2015 |
Ludwig LS, Cho H, Wakabayashi A, Eng JC, Ulirsch JC, Fleming MD, Lodish HF, Sankaran VG. Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesis. American Journal of Hematology. 90: 386-91. PMID 25615569 DOI: 10.1002/Ajh.23952 |
0.426 |
|
| 2015 |
Bianchi P, Fermo E, Eng JC, Ulirsch JC, Vercellati C, Braidotti P, Hildick-Smith G, Satchwell TJ, Pellegrin S, Zanella A, Barcellini W, Paw BH, Toye AM, Sankaran VG. Biallelic Mutations in PARP4 Are Linked to a Variant Form of Congenital Dyserythropoietic Anemia Blood. 126: 272-272. DOI: 10.1182/Blood.V126.23.272.272 |
0.391 |
|
| 2015 |
Steinberg Shemer O, Byrska-Bishop M, Ulirsch JC, Abdulmalik O, Yao Y, Kim AR, Gadue P, Kingsley PD, French D, Hardison RC, Palis J, Sankaran VG, Weiss MJ. Temporally Distinct Developmental Waves of Erythropoiesis from Human Pluripotent Stem Cells Blood. 126: 1170-1170. DOI: 10.1182/Blood.V126.23.1170.1170 |
0.365 |
|
| 2014 |
Ulirsch JC, Lacy JN, An X, Mohandas N, Mikkelsen TS, Sankaran VG. Altered chromatin occupancy of master regulators underlies evolutionary divergence in the transcriptional landscape of erythroid differentiation. Plos Genetics. 10: e1004890. PMID 25521328 DOI: 10.1371/Journal.Pgen.1004890 |
0.422 |
|
| 2014 |
Ludwig LS, Gazda HT, Eng JC, Eichhorn SW, Thiru P, Ghazvinian R, George TI, Gotlib JR, Beggs AH, Sieff CA, Lodish HF, Lander ES, Sankaran VG. Altered translation of GATA1 in Diamond-Blackfan anemia. Nature Medicine. 20: 748-53. PMID 24952648 DOI: 10.1038/Nm.3557 |
0.381 |
|
| 2014 |
Pishesha N, Thiru P, Shi J, Eng JC, Sankaran VG, Lodish HF. Transcriptional divergence and conservation of human and mouse erythropoiesis. Proceedings of the National Academy of Sciences of the United States of America. 111: 4103-8. PMID 24591581 DOI: 10.1073/Pnas.1401598111 |
0.421 |
|
| 2014 |
Sankaran VG. Post-Transcriptional Defects and Erythroid Pathobiology Blood. 124: SCI-35-SCI-35. DOI: 10.1182/Blood.V124.21.Sci-35.Sci-35 |
0.459 |
|
| 2014 |
Capellera Garcia S, Dhulipala K, Siva K, Rayon Estrada V, Wang E, Hyde G, Singbrant S, Walkley C, Soneji S, Sankaran VG, Flygare J. Direct Lineage Reprogramming of Murine Fibroblasts to Erythroid Progenitor Cells By Defined Factors Blood. 124: 246-246. DOI: 10.1182/Blood.V124.21.246.246 |
0.424 |
|
| 2013 |
Sankaran VG, Joshi M, Agrawal A, Schmitz-Abe K, Towne MC, Marinakis N, Markianos K, Berry GT, Agrawal PB. Rare complete loss of function provides insight into a pleiotropic genome-wide association study locus. Blood. 122: 3845-7. PMID 24288412 DOI: 10.1182/Blood-2013-09-528315 |
0.355 |
|
| 2013 |
Sankaran VG, Gallagher PG. Applications of high-throughput DNA sequencing to benign hematology. Blood. 122: 3575-3582. PMID 24021670 DOI: 10.1182/Blood-2013-07-460337 |
0.346 |
|
| 2013 |
Sankaran VG, Orkin SH. Genome-wide association studies of hematologic phenotypes: A window into human hematopoiesis Current Opinion in Genetics and Development. 23: 339-344. PMID 23477921 DOI: 10.1016/J.Gde.2013.02.006 |
0.53 |
|
| 2013 |
Musallam KM, Taher AT, Cappellini MD, Sankaran VG. Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia. Blood. 121: 2199-2212; quiz 2372. PMID 23315167 DOI: 10.1182/Blood-2012-10-408021 |
0.305 |
|
| 2013 |
Sankaran VG, Orkin SH. The switch from fetal to adult hemoglobin Cold Spring Harbor Perspectives in Medicine. 3. PMID 23209159 DOI: 10.1101/Cshperspect.A011643 |
0.504 |
|
| 2012 |
Sankaran VG, Ludwig LS, Sicinska E, Xu J, Bauer DE, Eng JC, Patterson HC, Metcalf RA, Natkunam Y, Orkin SH, Sicinski P, Lander ES, Lodish HF. Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number. Genes & Development. 26: 2075-87. PMID 22929040 DOI: 10.1101/Gad.197020.112 |
0.55 |
|
| 2012 |
Sankaran VG, Ghazvinian R, Do R, Thiru P, Vergilio JA, Beggs AH, Sieff CA, Orkin SH, Nathan DG, Lander ES, Gazda HT. Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia. The Journal of Clinical Investigation. 122: 2439-43. PMID 22706301 DOI: 10.1172/Jci63597 |
0.518 |
|
| 2011 |
Sankaran VG. Targeted therapeutic strategies for fetal hemoglobin induction. Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program. 2011: 459-465. PMID 22160074 DOI: 10.1182/Asheducation-2011.1.459 |
0.402 |
|
| 2011 |
Xu J, Peng C, Sankaran VG, Shao Z, Esrick EB, Chong BG, Ippolito GC, Fujiwara Y, Ebert BL, Tucker PW, Orkin SH. Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing. Science (New York, N.Y.). 334: 993-6. PMID 21998251 DOI: 10.1126/Science.1211053 |
0.528 |
|
| 2011 |
Sankaran VG, Xu J, Byron R, Greisman HA, Fisher C, Weatherall DJ, Sabath DE, Groudine M, Orkin SH, Premawardhena A, Bender MA. A functional element necessary for fetal hemoglobin silencing. The New England Journal of Medicine. 365: 807-14. PMID 21879898 DOI: 10.1056/Nejmoa1103070 |
0.51 |
|
| 2011 |
Sankaran VG, Menne J, Heller R. Heterozygous disruption of human SOX6 is insufficient to impair erythropoiesis or silencing of fetal hemoglobin Blood. 117: 4396-4397. PMID 21511965 DOI: 10.1182/Blood-2010-11-320887 |
0.428 |
|
| 2011 |
Sankaran VG, Menne TF, Šćepanović D, Vergilio JA, Ji P, Kim J, Thiru P, Orkin SH, Lander ES, Lodish HF. MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13. Proceedings of the National Academy of Sciences of the United States of America. 108: 1519-24. PMID 21205891 DOI: 10.1073/Pnas.1018384108 |
0.537 |
|
| 2011 |
Wilber A, Hargrove PW, Kim YS, Riberdy JM, Sankaran VG, Papanikolaou E, Georgomanoli M, Anagnou NP, Orkin SH, Nienhuis AW, Persons DA. Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34+ cells after lentiviral vector-mediated gene transfer. Blood. 117: 2817-26. PMID 21156846 DOI: 10.1182/Blood-2010-08-300723 |
0.536 |
|
| 2011 |
Xu J, Peng C, Sankaran VG, Orkin SH. Correction of Murine Sickle Cell Disease Through Interference with Fetal Hemoglobin Silencing Blood. 118: 351-351. DOI: 10.1182/Blood.V118.21.351.351 |
0.504 |
|
| 2010 |
Sankaran VG, Nathan DG. Reversing the hemoglobin switch. The New England Journal of Medicine. 363: 2258-60. PMID 21121839 DOI: 10.1056/Nejmcibr1010767 |
0.379 |
|
| 2010 |
Sankaran VG, Nathan DG. Thalassemia: an overview of 50 years of clinical research. Hematology/Oncology Clinics of North America. 24: 1005-20. PMID 21075277 DOI: 10.1016/J.Hoc.2010.08.009 |
0.32 |
|
| 2010 |
Galarneau G, Palmer CD, Sankaran VG, Orkin SH, Hirschhorn JN, Lettre G. Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation Nature Genetics. 42: 1049-1051. PMID 21057501 DOI: 10.1038/Ng.707 |
0.5 |
|
| 2010 |
Sankaran VG, Lettre G, Orkin SH, Hirschhorn JN. Modifier genes in Mendelian disorders: the example of hemoglobin disorders. Annals of the New York Academy of Sciences. 1214: 47-56. PMID 21039591 DOI: 10.1111/J.1749-6632.2010.05821.X |
0.525 |
|
| 2010 |
Sankaran VG, Xu J, Orkin SH. Transcriptional silencing of fetal hemoglobin by BCL11A. Annals of the New York Academy of Sciences. 1202: 64-8. PMID 20712774 DOI: 10.1111/J.1749-6632.2010.05574.X |
0.574 |
|
| 2010 |
Xu J, Sankaran VG, Ni M, Menne TF, Puram RV, Kim W, Orkin SH. Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6. Genes & Development. 24: 783-98. PMID 20395365 DOI: 10.1101/Gad.1897310 |
0.513 |
|
| 2010 |
Sankaran VG, Xu J, Orkin SH. Advances in the understanding of haemoglobin switching. British Journal of Haematology. 149: 181-94. PMID 20201948 DOI: 10.1111/J.1365-2141.2010.08105.X |
0.511 |
|
| 2010 |
Xu J, Sankaran VG, Esrick EB, Ebert BL, Orkin SH. Reactivation of Silenced Human HbF In Adult Mice by Inactivation of BCL11A Blood. 116: 643-643. DOI: 10.1182/Blood.V116.21.643.643 |
0.46 |
|
| 2009 |
Sankaran VG, Xu J, Ragoczy T, Ippolito GC, Walkley CR, Maika SD, Fujiwara Y, Ito M, Groudine M, Bender MA, Tucker PW, Orkin SH. Developmental and species-divergent globin switching are driven by BCL11A. Nature. 460: 1093-7. PMID 19657335 DOI: 10.1038/Nature08243 |
0.533 |
|
| 2009 |
Xu J, Sankaran VG, Fujiwara Y, Orkin SH. Control of Hemoglobin Switching by BCL11A. Blood. 114: 5-5. DOI: 10.1182/Blood.V114.22.5.5 |
0.49 |
|
| 2008 |
Sankaran VG, Menne TF, Xu J, Akie TE, Lettre G, Van Handel B, Mikkola HK, Hirschhorn JN, Cantor AB, Orkin SH. Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A. Science (New York, N.Y.). 322: 1839-42. PMID 19056937 DOI: 10.1126/science.1165409 |
0.557 |
|
| 2008 |
Walkley CR, Sankaran VG, Orkin SH. Rb and hematopoiesis: stem cells to anemia. Cell Division. 3: 13. PMID 18775080 DOI: 10.1186/1747-1028-3-13 |
0.54 |
|
| 2008 |
Lettre G, Sankaran VG, Bezerra MA, Araújo AS, Uda M, Sanna S, Cao A, Schlessinger D, Costa FF, Hirschhorn JN, Orkin SH. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America. 105: 11869-74. PMID 18667698 DOI: 10.1073/Pnas.0804799105 |
0.472 |
|
| 2008 |
Walkley CR, Qudsi R, Sankaran VG, Perry JA, Gostissa M, Roth SI, Rodda SJ, Snay E, Dunning P, Fahey FH, Alt FW, McMahon AP, Orkin SH. Conditional mouse osteosarcoma, dependent on p53 loss and potentiated by loss of Rb, mimics the human disease. Genes & Development. 22: 1662-76. PMID 18559481 DOI: 10.1101/Gad.1656808 |
0.529 |
|
| 2008 |
Sankaran VG, Orkin SH, Walkley CR. Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesis. Genes & Development. 22: 463-75. PMID 18258751 DOI: 10.1182/Blood.V110.11.638.638 |
0.49 |
|
| 2008 |
Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, et al. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. Proceedings of the National Academy of Sciences of the United States of America. 105: 1620-5. PMID 18245381 DOI: 10.1073/Pnas.0711566105 |
0.53 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2024 |
Weng C, Yu F, Yang D, Poeschla M, Liggett LA, Jones MG, Qiu X, Wahlster L, Caulier A, Hussmann JA, Schnell A, Yost KE, Koblan L, Martin-Rufino JD, Min J, ... ... Sankaran VG, et al. Deciphering cell states and genealogies of human hematopoiesis. Nature. PMID 38253266 DOI: 10.1038/s41586-024-07066-z |
0.297 |
|
| 2022 |
Wen J, Lagler TM, Sun Q, Yang Y, Chen J, Harigaya Y, Sankaran VG, Hu M, Reiner AP, Raffield LM, Li Y. Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types. Plos Genetics. 18: e1009984. PMID 35100265 DOI: 10.1371/journal.pgen.1009984 |
0.296 |
|
| 2016 |
Narla A, Yuan D, Kazerounian S, LaVasseur C, Ulirsch JC, Narla J, Glader B, Sankaran VG, Gazda H. A novel pathogenic mutation in RPL11 identified in a patient diagnosed with diamond Blackfan anemia as a young adult. Blood Cells, Molecules & Diseases. 61: 46-7. PMID 27667165 DOI: 10.1016/J.Bcmd.2016.08.001 |
0.295 |
|
| 2017 |
Ulirsch JC, Lareau C, Ludwig LS, Mohandas N, Nathan DG, Sankaran VG. Confounding in ex vivo models of Diamond-Blackfan anemia. Blood. PMID 28615220 DOI: 10.1182/Blood-2017-05-783191 |
0.29 |
|
| 2011 |
Singbrant S, Russell MR, Jovic T, Liddicoat B, Izon DJ, Purton LE, Sims NA, Martin TJ, Sankaran VG, Walkley CR. Erythropoietin couples erythropoiesis, B-lymphopoiesis, and bone homeostasis within the bone marrow microenvironment Blood. 117: 5631-5642. PMID 21421837 DOI: 10.1182/Blood-2010-11-320564 |
0.286 |
|
| 2021 |
Martin-Rufino JD, Sankaran VG. Deciphering transcriptional and functional heterogeneity in hematopoiesis with single-cell genomics. Current Opinion in Hematology. 28: 269-276. PMID 33901135 DOI: 10.1097/MOH.0000000000000657 |
0.285 |
|
| 2022 |
Sun Q, Crowley CA, Huang L, Wen J, Chen J, Bao EL, Auer PL, Lettre G, Reiner AP, Sankaran VG, Raffield LM, Li Y. From GWAS variant to function: A study of ∼148,000 variants for blood cell traits. Hgg Advances. 3: 100063. PMID 35047852 DOI: 10.1016/j.xhgg.2021.100063 |
0.285 |
|
| 2012 |
Zhang L, Sankaran VG, Lodish HF. MicroRNAs in erythroid and megakaryocytic differentiation and megakaryocyte-erythroid progenitor lineage commitment. Leukemia. 26: 2310-6. PMID 22617791 DOI: 10.1038/Leu.2012.137 |
0.283 |
|
| 2017 |
Allam R, Chennupati V, Veiga D, Maslowski K, Tardivel A, Andina N, Chi-Wang Yu E, Stilinovic M, Simillion C, Duchosal M, Quadroni M, Roberts I, Sankaran V, MacDonald HR, Fasel N, et al. Ribonuclease inhibitor (RNH1) is a ribosome-associated protein and regulates erythropoiesis by controlling GATA1-specific mRNA translation Experimental Hematology. 53: S133. DOI: 10.1016/J.Exphem.2017.06.338 |
0.283 |
|
| 2022 |
Yu F, Cato LD, Weng C, Liggett LA, Jeon S, Xu K, Chiang CWK, Wiemels JL, Weissman JS, de Smith AJ, Sankaran VG. Variant to function mapping at single-cell resolution through network propagation. Nature Biotechnology. PMID 35668323 DOI: 10.1038/s41587-022-01341-y |
0.282 |
|
| 2023 |
Lozano Chinga MM, Bertuch AA, Afify Z, Dollerschell K, Hsu JI, John TD, Rao ES, Rowe RG, Sankaran VG, Shimamura A, Williams DA, Nakano TA. Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM-associated syndromes. American Journal of Medical Genetics. Part A. PMID 37067177 DOI: 10.1002/ajmg.a.63208 |
0.281 |
|
| 2012 |
Musallam KM, Sankaran VG, Cappellini MD, Duca L, Nathan DG, Taher AT. Fetal hemoglobin levels and morbidity in untransfused patients with β-thalassemia intermedia. Blood. 119: 364-7. PMID 22096240 DOI: 10.1182/Blood-2011-09-382408 |
0.278 |
|
| 2020 |
Voit RA, Sankaran VG. Stabilizing HIF to Ameliorate Anemia. Cell. 180: 6. PMID 31951520 DOI: 10.1016/J.Cell.2019.12.010 |
0.275 |
|
| 2023 |
Lareau CA, Liu V, Muus C, Praktiknjo SD, Nitsch L, Kautz P, Sandor K, Yin Y, Gutierrez JC, Pelka K, Satpathy AT, Regev A, Sankaran VG, Ludwig LS. Mitochondrial single-cell ATAC-seq for high-throughput multi-omic detection of mitochondrial genotypes and chromatin accessibility. Nature Protocols. PMID 36792778 DOI: 10.1038/s41596-022-00795-3 |
0.27 |
|
| 2022 |
Rowland B, Venkatesh S, Tardaguila M, Wen J, Rosen JD, Tapia AL, Sun Q, Graff M, Vuckovic D, Lettre G, Sankaran VG, Voloudakis G, Roussos P, Huffman JE, Reiner AP, et al. Transcriptome-wide association study in UK biobank Europeans identifies associations with blood cell traits. Human Molecular Genetics. PMID 35138379 DOI: 10.1093/hmg/ddac011 |
0.267 |
|
| 2022 |
Hujoel MLA, Sherman MA, Barton AR, Mukamel RE, Sankaran VG, Terao C, Loh PR. Influences of rare copy-number variation on human complex traits. Cell. 185: 4233-4248.e27. PMID 36306736 DOI: 10.1016/j.cell.2022.09.028 |
0.266 |
|
| 2023 |
Bloom M, Malouf C, Rodriguez-Fraticelli A, Wilkinson AC, Sankaran VG, Cvejic A. Exploiting somatic mutations to decipher human blood production: a natural lineage-tracing strategy. Experimental Hematology. PMID 36736573 DOI: 10.1016/j.exphem.2023.01.005 |
0.264 |
|
| 2022 |
Lopez de Lapuente Portilla A, Ekdahl L, Cafaro C, Ali Z, Miharada N, Thorleifsson G, Žemaitis K, Lamarca Arrizabalaga A, Thodberg M, Pertesi M, Dhapola P, Bao EL, Niroula A, Bali D, Norddahl GL, ... ... Sankaran VG, et al. Genome-wide association study on 13,167 individuals identifies regulators of blood CD34+ cell levels. Blood. PMID 35007327 DOI: 10.1182/blood.2021013220 |
0.264 |
|
| 2021 |
Penter L, Gohil SH, Lareau C, Ludwig LS, Parry EM, Huang T, Li S, Zhang W, Livitz D, Leshchiner I, Parida L, Getz G, Rassenti LZ, Kipps TJ, Brown JR, ... ... Sankaran VG, et al. Longitudinal single-cell dynamics of chromatin accessibility and mitochondrial mutations in chronic lymphocytic leukemia mirror disease history. Cancer Discovery. PMID 34112698 DOI: 10.1158/2159-8290.CD-21-0276 |
0.263 |
|
| 2023 |
Lareau CA, Dubois SM, Buquicchio FA, Hsieh YH, Garg K, Kautz P, Nitsch L, Praktiknjo SD, Maschmeyer P, Verboon JM, Gutierrez JC, Yin Y, Fiskin E, Luo W, Mimitou EP, ... ... Sankaran VG, et al. Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells. Nature Genetics. PMID 37386249 DOI: 10.1038/s41588-023-01433-8 |
0.262 |
|
| 2012 |
Sankaran VG, Sapp MV. Persistence of fetal hemoglobin expression in an older child with trisomy 13 Journal of Pediatrics. 160: 352. PMID 21885064 DOI: 10.1016/J.Jpeds.2011.07.036 |
0.258 |
|
| 2022 |
Gupta A, Martin-Rufino JD, Jones TR, Subramanian V, Qiu X, Grody EI, Bloemendal A, Weng C, Niu SY, Min KH, Mehta A, Zhang K, Siraj L, Al' Khafaji A, Sankaran VG, et al. Inferring gene regulation from stochastic transcriptional variation across single cells at steady state. Proceedings of the National Academy of Sciences of the United States of America. 119: e2207392119. PMID 35969771 DOI: 10.1073/pnas.2207392119 |
0.254 |
|
| 2022 |
Ajore R, Niroula A, Pertesi M, Cafaro C, Thodberg M, Went M, Bao EL, Duran-Lozano L, Lopez de Lapuente Portilla A, Olafsdottir T, Ugidos-Damboriena N, Magnusson O, Samur M, Lareau CA, Halldorsson GH, ... ... Sankaran VG, et al. Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature Communications. 13: 151. PMID 35013207 DOI: 10.1038/s41467-021-27666-x |
0.251 |
|
| 2021 |
Mimitou EP, Lareau CA, Chen KY, Zorzetto-Fernandes AL, Hao Y, Takeshima Y, Luo W, Huang TS, Yeung BZ, Papalexi E, Thakore PI, Kibayashi T, Wing JB, Hata M, Satija R, ... ... Sankaran VG, et al. Scalable, multimodal profiling of chromatin accessibility, gene expression and protein levels in single cells. Nature Biotechnology. PMID 34083792 DOI: 10.1038/s41587-021-00927-2 |
0.25 |
|
| 2020 |
Hou L, Voit RA, Sankaran VG, Springer TA, Yuki K. CD11c regulates hematopoietic stem and progenitor cells under stress. Blood Advances. 4: 6086-6097. PMID 33351105 DOI: 10.1182/bloodadvances.2020002504 |
0.248 |
|
| 2023 |
Zhao J, Jia Y, Mahmut D, Deik AA, Jeanfavre S, Clish CB, Sankaran VG. Human hematopoietic stem cell vulnerability to ferroptosis. Cell. 186: 732-747.e16. PMID 36803603 DOI: 10.1016/j.cell.2023.01.020 |
0.247 |
|
| 2007 |
Sankaran VG, Walkley CR, Spiegelman BM, Orkin SH. Rb Intrinsically Promotes Erythropoiesis by Coupling Cell Cycle Exit with Mitochondrial Biogenesis. Blood. 110: 638-638. DOI: 10.1182/blood.v110.11.638.638 |
0.245 |
|
| 2010 |
Sankaran VG. Hemoglobin disorders in the developing world: a perspective from Sri Lanka. American Journal of Hematology. 85: 732. PMID 20645427 DOI: 10.1002/Ajh.21769 |
0.245 |
|
| 2022 |
Ditadi A, Sankaran VG. Vade-MECOM: How to peel back the layers of hematopoiesis. Cell Stem Cell. 29: 1512-1514. PMID 36332568 DOI: 10.1016/j.stem.2022.10.007 |
0.245 |
|
| 2023 |
Martell DJ, Merens HE, Fiorini C, Caulier A, Ulirsch JC, Ietswaart R, Choquet K, Graziadei G, Brancaleoni V, Domenica Cappellini M, Scott C, Roberts N, Proven M, Roy NB, Babbs C, ... ... Sankaran VG, et al. RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation. Medrxiv : the Preprint Server For Health Sciences. PMID 36945604 DOI: 10.1101/2023.03.03.23286760 |
0.244 |
|
| 2023 |
Voit RA, Sankaran VG. MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development. Journal of Clinical Immunology. 43: 1052-1066. PMID 37407873 DOI: 10.1007/s10875-023-01545-0 |
0.244 |
|
| 2018 |
Raffield LM, Ulirsch JC, Naik RP, Lessard S, Handsaker RE, Jain D, Kang HM, Pankratz N, Auer PL, Bao EL, Smith JD, Lange LA, Lange EM, Li Y, Thornton TA, ... ... Sankaran VG, et al. Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. Plos Genetics. 14: e1007293. PMID 29590102 DOI: 10.1371/journal.pgen.1007293 |
0.24 |
|
| 2019 |
Zhang S, Macias-Garcia A, Ulirsch JC, Velazquez J, Butty VL, Levine SS, Sankaran VG, Chen J. Author response: HRI coordinates translation necessary for protein homeostasis and mitochondrial function in erythropoiesis Elife. DOI: 10.7554/Elife.46976.029 |
0.239 |
|
| 2015 |
Sabath DE, Bender MA, Sankaran VG, Vamos E, Kentsis A, Yi HS, Greisman HA. Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization. The Journal of Molecular Diagnostics : Jmd. PMID 26612711 DOI: 10.1016/J.Jmoldx.2015.07.011 |
0.236 |
|
| 2021 |
Yu F, Sankaran VG, Yuan GC. CUT&RUNTools 2.0: A pipeline for single-cell and bulk-level CUT&RUN and CUT&Tag data analysis. Bioinformatics (Oxford, England). PMID 34244724 DOI: 10.1093/bioinformatics/btab507 |
0.232 |
|
| 2019 |
Mohan K, Ueda G, Kim AR, Jude KM, Fallas JA, Guo Y, Hafer M, Miao Y, Saxton RA, Piehler J, Sankaran VG, Baker D, Garcia KC. Topological control of cytokine receptor signaling induces differential effects in hematopoiesis. Science (New York, N.Y.). 364. PMID 31123111 DOI: 10.1126/Science.Aav7532 |
0.23 |
|
| 2023 |
Sun Q, Rowland B, Wang W, Miller-Fleming TW, Cox N, Graff M, Faucon A, Shuey MM, Blue EE, Auer P, Li Y, Sankaran VG, Reiner AP, Raffield LM. Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19. Blood Cells, Molecules & Diseases. 103: 102782. PMID 37558590 DOI: 10.1016/j.bcmd.2023.102782 |
0.23 |
|
| 2022 |
Miller TE, Lareau CA, Verga JA, DePasquale EAK, Liu V, Ssozi D, Sandor K, Yin Y, Ludwig LS, El Farran CA, Morgan DM, Satpathy AT, Griffin GK, Lane AA, Love JC, ... ... Sankaran VG, et al. Mitochondrial variant enrichment from high-throughput single-cell RNA sequencing resolves clonal populations. Nature Biotechnology. PMID 35210612 DOI: 10.1038/s41587-022-01210-8 |
0.227 |
|
| 2020 |
Bao EL, Nandakumar SK, Liao X, Bick AG, Karjalainen J, Tabaka M, Gan OI, Havulinna AS, Kiiskinen TTJ, Lareau CA, de Lapuente Portilla AL, Li B, Emdin C, Codd V, Nelson CP, ... ... Sankaran VG, et al. Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. Nature. PMID 33057200 DOI: 10.1038/s41586-020-2786-7 |
0.227 |
|
| 2019 |
Ozcan A, Saracoglu S, Verboon J, Karakukcu M, Patiroglu T, Coskun A, Sankaran V, Unal E. A mummy emerges from the grave: Scurvy confounding the clinical presentation of a child with Fanconi Anemia. American Journal of Hematology. PMID 30637794 DOI: 10.1002/Ajh.25402 |
0.226 |
|
| 2018 |
Musunuru K, Bernstein D, Cole FS, Khokha MK, Lee FS, Lin S, McDonald TV, Moskowitz IP, Quertermous T, Sankaran VG, Schwartz DA, Silverman EK, Zhou X, Hasan AAK, Luo XJ. Functional Assays to Screen and Dissect Genomic Hits: Doubling Down on the National Investment in Genomic Research. Circulation. Genomic and Precision Medicine. 11: e002178. PMID 29654098 DOI: 10.1161/CIRCGEN.118.002178 |
0.225 |
|
| 2023 |
Jun G, English A, Metcalf G, Yang J, Chaisson M, Pankratz N, Menon V, Salerno W, Krasheninina O, Smith A, Lane J, Blackwell T, Kang HM, Salvi S, Meng Q, ... ... Sankaran V, et al. Structural variation across 138,134 samples in the TOPMed consortium. Research Square. PMID 36778386 DOI: 10.21203/rs.3.rs-2515453/v1 |
0.224 |
|
| 2023 |
Jun G, English AC, Metcalf GA, Yang J, Chaisson MJ, Pankratz N, Menon VK, Salerno WJ, Krasheninina O, Smith AV, Lane JA, Blackwell T, Kang HM, Salvi S, Meng Q, ... ... Sankaran VG, et al. Structural variation across 138,134 samples in the TOPMed consortium. Biorxiv : the Preprint Server For Biology. PMID 36747810 DOI: 10.1101/2023.01.25.525428 |
0.223 |
|
| 2000 |
Ferguson KM, Kavran JM, Sankaran VG, Fournier E, Isakoff SJ, Skolnik EY, Lemmon MA. Structural basis for discrimination of 3-phosphoinositides by pleckstrin homology domains. Molecular Cell. 6: 373-84. PMID 10983984 DOI: 10.1016/S1097-2765(00)00037-X |
0.222 |
|
| 2001 |
Sankaran VG, Klein DE, Sachdeva MM, Lemmon MA. High-affinity binding of a FYVE domain to phosphatidylinositol 3-phosphate requires intact phospholipid but not FYVE domain oligomerization. Biochemistry. 40: 8581-7. PMID 11456498 DOI: 10.1021/Bi010425D |
0.218 |
|
| 2023 |
Martell DJ, Merens HE, Caulier A, Fiorini C, Ulirsch JC, Ietswaart R, Choquet K, Graziadei G, Brancaleoni V, Cappellini MD, Scott C, Roberts N, Proven M, Roy NBA, Babbs C, ... ... Sankaran VG, et al. RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation. Developmental Cell. PMID 37586368 DOI: 10.1016/j.devcel.2023.07.018 |
0.217 |
|
| 2021 |
Wahlster L, Sankaran VG. I SPI1 something needed for B cells. The Journal of Experimental Medicine. 218. PMID 33978700 DOI: 10.1084/jem.20210572 |
0.215 |
|
| 2020 |
Wahlster L, Weichert-Leahey N, Trissal M, Grace RF, Sankaran VG. COVID-19 presenting with autoimmune hemolytic anemia in the setting of underlying immune dysregulation. Pediatric Blood & Cancer. e28382. PMID 32495391 DOI: 10.1002/Pbc.28382 |
0.214 |
|
| 2021 |
Wahlster L, Verboon JM, Ludwig LS, Black SC, Luo W, Garg K, Voit RA, Collins RL, Garimella K, Costello M, Chao KR, Goodrich JK, DiTroia SP, O'Donnell-Luria A, Talkowski ME, ... ... Sankaran VG, et al. Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript. The Journal of Experimental Medicine. 218. PMID 33857290 DOI: 10.1084/jem.20210444 |
0.209 |
|
| 2017 |
Steinberg-Shemer O, Ulirsch JC, Noy-Lotan S, Krasnov T, Attias D, Dgany O, Laor R, Sankaran VG, Tamary H. Whole exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia. Cold Spring Harbor Molecular Case Studies. PMID 28667000 DOI: 10.1101/mcs.a001941 |
0.203 |
|
| 2020 |
Walker MA, Lareau CA, Ludwig LS, Karaa A, Sankaran VG, Regev A, Mootha VK. Purifying Selection against Pathogenic Mitochondrial DNA in Human T Cells. The New England Journal of Medicine. PMID 32786181 DOI: 10.1056/NEJMoa2001265 |
0.193 |
|
| 2023 |
Lemire G, Sanchis-Juan A, Russell K, Baxter S, Chao KR, Singer-Berk M, Groopman E, Wong I, England E, Goodrich J, Pais L, Austin-Tse C, DiTroia S, O'Heir E, Ganesh VS, ... ... Sankaran VG, et al. Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37873196 DOI: 10.1101/2023.10.05.23296595 |
0.19 |
|
| 2016 |
Joshi M, Anselm I, Shi J, Bale TA, Towne M, Schmitz-Abe K, Crowley L, Giani FC, Kazerounian S, Markianos K, Lidov HG, Folkerth R, Sankaran VG, Agrawal PB. Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-α protein (PMPCA) cause a severe mitochondrial disease. Cold Spring Harbor Molecular Case Studies. 2: a000786. PMID 27148589 DOI: 10.1101/mcs.a000786 |
0.188 |
|
| 2021 |
Ejaz A, Ozcan A, Unal E, Karakukcu M, Sankaran VG. Long-Term Patient-Customized Therapy for a Pathogenic Mutation. Med (New York, N.Y.). 2: 33-37.e1. PMID 33521754 DOI: 10.1016/j.medj.2020.10.001 |
0.188 |
|
| 2024 |
Dai E, Chen X, Linkermann A, Jiang X, Kang R, Kagan VE, Bayir H, Yang WS, Garcia-Saez AJ, Ioannou MS, Janowitz T, Ran Q, Gu W, Gan B, Krysko DV, ... ... Sankaran VG, et al. A guideline on the molecular ecosystem regulating ferroptosis. Nature Cell Biology. PMID 38424270 DOI: 10.1038/s41556-024-01360-8 |
0.188 |
|
| 2013 |
Sankaran VG, Agrawal PB. Stimulating erythropoiesis in neonates American Journal of Hematology. 88: 930-931. PMID 23963872 DOI: 10.1002/Ajh.23573 |
0.186 |
|
| 2023 |
Zhang H, Yu X, Ye J, Li H, Hu J, Tan Y, Fang Y, Akbay E, Yu F, Weng C, Sankaran VG, Bachoo RM, Maher E, Minna J, Zhang A, et al. Systematic investigation of mitochondrial transfer between cancer cells and T cells at single-cell resolution. Cancer Cell. 41: 1788-1802.e10. PMID 37816332 DOI: 10.1016/j.ccell.2023.09.003 |
0.186 |
|
| 2022 |
Qiu X, Zhang Y, Martin-Rufino JD, Weng C, Hosseinzadeh S, Yang D, Pogson AN, Hein MY, Hoi Joseph Min K, Wang L, Grody EI, Shurtleff MJ, Yuan R, Xu S, Ma Y, ... ... Sankaran VG, et al. Mapping transcriptomic vector fields of single cells. Cell. PMID 35108499 DOI: 10.1016/j.cell.2021.12.045 |
0.185 |
|
| 2023 |
Sozen B, Flavell RA, Lamming DW, Silver DL, Parrinello S, Abate-Shen C, Michor F, Sankaran VG. What approaches are needed to understand human development and disease? Developmental Cell. 58: 2822-2825. PMID 38113848 DOI: 10.1016/j.devcel.2023.11.026 |
0.183 |
|
| 2022 |
Hou L, Voit RA, Shibamura-Fujiogi M, Koutsogiannaki S, Li Y, Chen Y, Luo HR, Sankaran VG, Yuki K. CD11c regulates neutrophil maturation. Blood Advances. PMID 36306384 DOI: 10.1182/bloodadvances.2022007719 |
0.18 |
|
| 2023 |
Wojcik MH, Lemire G, Zaki MS, Wissman M, Win W, White S, Weisburd B, Waddell LB, Verboon JM, VanNoy GE, Töpf A, Tan TY, Straub V, Stenton SL, Snow H, ... ... Sankaran VG, et al. Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis. Medrxiv : the Preprint Server For Health Sciences. PMID 38328047 DOI: 10.1101/2023.08.08.23293829 |
0.18 |
|
| 2023 |
Joubran S, Sankaran VG. Getting an aMPLe grasp on hematopoiesis. Cell. 186: 4005-4006. PMID 37714132 DOI: 10.1016/j.cell.2023.08.015 |
0.176 |
|
| 2021 |
Hasle H, Kline RM, Kjeldsen E, Nik-Abdul-Rashid NF, Bhojwani D, Verboon JM, DiTroia SP, Chao KR, Raaschou-Jensen K, Palle J, Zwaan CM, Nyvold CG, Sankaran VG, Cantor AB. Germline GATA1s generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotype. Blood. PMID 34758059 DOI: 10.1182/blood.2021011463 |
0.174 |
|
| 2015 |
Basak A, Hancarova M, Ulirsch JC, Balci TB, Trkova M, Pelisek M, Vlckova M, Muzikova K, Cermak J, Trka J, Dyment DA, Orkin SH, Daly MJ, Sedlacek Z, Sankaran VG. BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations Journal of Clinical Investigation. 125: 2363-2368. DOI: 10.1172/JCI81163 |
0.174 |
|
| 2022 |
Liggett LA, Cato LD, Weinstock JS, Zhang Y, Nouraie SM, Gladwin MT, Garrett ME, Ashley-Koch A, Telen M, Custer B, Kelly S, Dinardo C, Sabino EC, Loureiro P, Carneiro-Proietti A, ... ... Sankaran VG, et al. Clonal hematopoiesis in sickle cell disease. The Journal of Clinical Investigation. PMID 34990411 DOI: 10.1172/JCI156060 |
0.173 |
|
| 2016 |
Lacy JN, Ulirsch JC, Grace RF, Towne MC, Hale J, Mohandas N, Lux SE, Agrawal PB, Sankaran VG. Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia. Cold Spring Harbor Molecular Case Studies. 2: a000885. PMID 27551681 DOI: 10.1101/mcs.a000885 |
0.166 |
|
| 2019 |
Ulirsch JC, Verboon JM, Kazerounian S, Guo MH, Yuan D, Ludwig LS, Handsaker RE, Abdulhay NJ, Fiorini C, Genovese G, Lim ET, Cheng A, Cummings BB, Chao KR, Beggs AH, ... ... Sankaran VG, et al. The Genetic Landscape of Diamond-Blackfan Anemia. American Journal of Human Genetics. 104: 356. PMID 30735661 DOI: 10.1016/j.ajhg.2018.12.011 |
0.153 |
|
| 2023 |
Brown DW, Cato LD, Zhao Y, Nandakumar SK, Bao EL, Gardner EJ, Hubbard AK, DePaulis A, Rehling T, Song L, Yu K, Chanock SJ, Perry JRB, Sankaran VG, Machiela MJ. Shared and distinct genetic etiologies for different types of clonal hematopoiesis. Nature Communications. 14: 5536. PMID 37684235 DOI: 10.1038/s41467-023-41315-5 |
0.147 |
|
| 2023 |
Liu A, Genovese G, Zhao Y, Pirinen M, Zekavat MM, Kentistou K, Yang Z, Yu K, Vlasschaert C, Liu X, Brown DW, Hudjashov G, Gorman B, Dennis J, Zhou W, ... ... Sankaran VG, et al. Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection. Medrxiv : the Preprint Server For Health Sciences. PMID 36778285 DOI: 10.1101/2023.01.28.23285140 |
0.147 |
|
| 2022 |
Liggett LA, Sankaran VG. Patchwork Cancer Predisposition. Cancer Discovery. 12: 889-891. PMID 35373283 DOI: 10.1158/2159-8290.CD-22-0025 |
0.145 |
|
| 2021 |
McGraw CM, Mahida S, Jayakar P, Koh HY, Taylor A, Resnick T, Rodan L, Schwartz MA, Ejaz A, Sankaran VG, Berry G, Poduri A. Uridine-responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings. Annals of Clinical and Translational Neurology. PMID 33497533 DOI: 10.1002/acn3.51272 |
0.135 |
|
| 2021 |
Musallam KM, Vitrano A, Meloni A, Addario Pollina S, Di Marco V, Hussain Ansari S, Filosa A, Ricchi P, Ceci A, Daar S, Vlachaki E, Singer ST, Naserullah ZA, Pepe A, Scondotto S, ... ... Sankaran VG, et al. Primary HBB gene mutation severity and long-term outcomes in a global cohort of β-thalassaemia. British Journal of Haematology. PMID 34697800 DOI: 10.1111/bjh.17897 |
0.122 |
|
| 2022 |
Alsavaf MB, Verboon JM, Dogan ME, Azizoglu ZB, Okus FZ, Ozcan A, Dundar M, Eken A, Donmez-Altuntas H, Sankaran VG, Unal E. A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome. British Journal of Haematology. PMID 35298850 DOI: 10.1111/bjh.18112 |
0.121 |
|
| 2023 |
Benz EJ, Sankaran VG. Thalassemia. Hematology/Oncology Clinics of North America. 37: xiii-xv. PMID 36907615 DOI: 10.1016/j.hoc.2023.01.001 |
0.121 |
|
| 2024 |
de Smith AJ, Wahlster L, Jeon S, Kachuri L, Black S, Langie J, Cato LD, Nakatsuka N, Chan TF, Xia G, Mazumder S, Yang W, Gazal S, Eng C, Hu D, ... ... Sankaran VG, et al. A noncoding regulatory variant in IKZF1 increases acute lymphoblastic leukemia risk in Hispanic/Latino children. Cell Genomics. 100526. PMID 38537633 DOI: 10.1016/j.xgen.2024.100526 |
0.12 |
|
| 2023 |
Lareau CA, Ludwig LS, Muus C, Gohil SH, Zhao T, Chiang Z, Pelka K, Verboon JM, Luo W, Christian E, Rosebrock D, Getz G, Boland GM, Chen F, Buenrostro JD, ... ... Sankaran VG, et al. Author Correction: Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling. Nature Biotechnology. PMID 37653227 DOI: 10.1038/s41587-023-01942-1 |
0.12 |
|
| 2023 |
Gold NB, Adelson SM, Shah N, Williams S, Bick SL, Zoltick ES, Gold JI, Strong A, Ganetzky R, Roberts AE, Walker M, Holtz AM, Sankaran VG, Delmonte O, Tan W, et al. Perspectives of Rare Disease Experts on Newborn Genome Sequencing. Jama Network Open. 6: e2312231. PMID 37155167 DOI: 10.1001/jamanetworkopen.2023.12231 |
0.118 |
|
| 2021 |
Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Niroula A, ... ... Sankaran VG, et al. Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. PMID 33707633 DOI: 10.1038/s41586-021-03280-1 |
0.117 |
|
| 2019 |
Yilmaz E, Ozcan A, Verboon JM, Karakukcu M, Sankaran VG, Unal E, Patıroglu T. A TURKISH CHILD PRESENTED WITH NEONATAL THROMBOCYTOPENIA ASSOCIATED WITH GNE MUTATION WITHOUT ASSOCIATED MUSCLE WASTING Hemasphere. 3: 848-849. DOI: 10.1097/01.HS9.0000565944.96087.88 |
0.101 |
|
| 2022 |
Rowland B, Sun Q, Wang W, Miller-Fleming T, Cox N, Graff M, Faucon A, Shuey MM, Blue EE, Auer P, Li Y, Sankaran VG, Reiner AP, Raffield LM. Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19. Medrxiv : the Preprint Server For Health Sciences. PMID 35262092 DOI: 10.1101/2022.02.28.22271562 |
0.096 |
|
| 2021 |
Musallam KM, Vitrano A, Meloni A, Pollina WA, Karimi M, El-Beshlawy A, Hajipour M, Di Marco V, Ansari SH, Filosa A, Ricchi P, Ceci A, Daar S, Vlachaki E, Singer ST, ... ... Sankaran VG, et al. Survival and causes of death in 2033 patients with non-transfusion-dependent β-thalassemia. Haematologica. PMID 33882642 DOI: 10.3324/haematol.2021.278684 |
0.093 |
|
| 2021 |
Sattar R, Ratha V, Kandallu SBR, Kapilavayi S, Sampath N, Sankaran V, Balasundaram P. Mature cystic teratoma of the right cerebellopontine angle: a rare case report. British Journal of Neurosurgery. 1-4. PMID 34410217 DOI: 10.1080/02688697.2021.1967287 |
0.088 |
|
| 2022 |
Vitrano A, Musallam KM, Meloni A, Karimi M, Daar S, Ricchi P, Costantini S, Vlachaki E, Di Marco V, El-Beshlawy A, Hajipour M, Ansari SH, Filosa A, Ceci A, Singer ST, ... ... Sankaran VG, et al. Development of a Thalassemia International Prognostic Scoring System (TIPSS). Blood Cells, Molecules & Diseases. 99: 102710. PMID 36463683 DOI: 10.1016/j.bcmd.2022.102710 |
0.088 |
|
| 2015 |
Sankaran VG, Weiss MJ. Anemia: Progress in molecular mechanisms and therapies Nature Medicine. 21: 221-230. DOI: 10.1038/nm.3814 |
0.086 |
|
| 2020 |
Meyts I, Bucciol G, Quinti I, Neven B, Fischer A, Seoane E, Lopez-Granados E, Gianelli C, Robles-Marhuenda A, Jeandel PY, Paillard C, Sankaran VG, Demirdag YY, Lougaris V, Aiuti A, et al. Coronavirus Disease 2019 in patients with inborn errors of immunity: an international study. The Journal of Allergy and Clinical Immunology. PMID 32980424 DOI: 10.1016/j.jaci.2020.09.010 |
0.086 |
|
| 2020 |
Sankaran VG, Ulirsch JC, Tchaikovskii V, Ludwig LS, Wakabayashi A, Kadirvel S, Lindsley RC, Bejar R, Shi J, Lovitch SB, Bishop DF, Steensma DP. X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation. The Journal of Clinical Investigation. 130: 552. PMID 31895053 DOI: 10.1172/JCI132538 |
0.084 |
|
| 2022 |
Ajore R, Niroula A, Pertesi M, Cafaro C, Thodberg M, Went M, Bao EL, Duran-Lozano L, Lopez de Lapuente Portilla A, Olafsdottir T, Ugidos-Damboriena N, Magnusson O, Samur M, Lareau CA, Halldorsson GH, ... ... Sankaran VG, et al. Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature Communications. 13: 7725. PMID 36513657 DOI: 10.1038/s41467-022-35411-1 |
0.081 |
|
| 2010 |
Fayeye O, Sankaran V, Sherlala K, Choksey M. Oligodendroglioma presenting with intradural spinal metastases: an unusual cause of cauda equina syndrome. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 17: 265-7. PMID 20042338 DOI: 10.1016/j.jocn.2009.05.029 |
0.067 |
|
| 2021 |
Musallam KM, Vitrano A, Meloni A, Pollina SA, Karimi M, El-Beshlawy A, Hajipour M, Di Marco V, Ansari SH, Filosa A, Ricchi P, Ceci A, Daar S, Vlachaki E, Singer ST, ... ... Sankaran VG, et al. Risk of mortality from anemia and iron overload in nontransfusion-dependent β-thalassemia. American Journal of Hematology. 97: E78-E80. PMID 34862982 DOI: 10.1002/ajh.26428 |
0.066 |
|
| 2019 |
Ratha V, Roopesh Kumar VR, Subramaniam S, Kumar S, Sankaran V, Suresh Bapu KR. Awake microvascular decompression with fat-teflon sandwich technique: Clinical implications of a novel approach for cranial nerve neuralgias. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. PMID 31014908 DOI: 10.1016/j.jocn.2019.04.007 |
0.06 |
|
| 2010 |
Sankaran V, Carey M, Shad A. Traumatic bleeding of spinal angiolipoma presenting with subacute paraparesis--a case report and histopathological aspects. British Journal of Neurosurgery. 24: 714-5. PMID 20874452 DOI: 10.3109/02688697.2010.520760 |
0.051 |
|
| 2018 |
Ilangovan VS, Kumar VRR, Sankaran V, Bapu KRS, Kapilavayi S. Aggressive Brainstem Glioblastoma in a 9-Year-Old Child with Neck Node Metastases: A Case Report and Review of Literature. Journal of Pediatric Neurosciences. 13: 234-236. PMID 30090145 DOI: 10.4103/jpn.JPN_160_17 |
0.048 |
|
| 2022 |
Voit RA, Sankaran VG. Multi-omics on our multitudes. Nature Genetics. 54: 1449-1450. PMID 36138230 DOI: 10.1038/s41588-022-01175-z |
0.027 |
|
| Hide low-probability matches. |