Erik Bao, MD
RESIDENT
Medicine
School of Medicine

Publications (25)

Top publication keywords:
SeizuresFamilyLarge Neutral Amino Acid-Transporter 1Genetic Predisposition to DiseaseGATA1 Transcription FactorMyeloproliferative DisordersAnticonvulsantsQuantitative Trait, HeritableTranscription Elongation, GeneticFetal HemoglobinHematopoietic Stem CellsBronchopulmonary DysplasiaAnemia, Sickle CellHematologic DiseasesHematopoiesis

• Inherited blood cancer predisposition through altered transcription elongation.
  Cell 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
• Shared and distinct genetic etiologies for different types of clonal hematopoiesis.
  Nature communications 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
• A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.
  Nature communications 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, Seyres D, Stegle O, Verboon JM, …
• Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.
  Nature communications 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, …
• Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1.
  Blood 2022 Ludwig LS, 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, Hunter A, Ogura H, Yamamoto T, Inada H, …

Show all (20 more) Hide

• Genome-wide association study on 13 167 individuals identifies regulators of blood CD34+cell levels.
  Blood 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 E, Niroula A, Bali D, Norddahl G, Ugidos …
• Functional dissection of inherited non-coding variation influencing multiple myeloma risk.
  Nature communications 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, …
• From GWAS variant to function: A study of ∼148,000 variants for blood cell traits.
  HGG advances 2021 Sun Q, Crowley CA, Huang L, Wen J, Chen J, Bao EL, Auer PL, Lettre G, Reiner AP, Sankaran VG, Raffield LM, Li Y
• Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
  Nature 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, Lin AE, Taub MA, Aguet F, Ardlie K, …
• Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
  Nature 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, Taub MA, Aguet F, Ardlie K, Mitchell BD…
• Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells.
  Nature 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, Walker CJ, Churchhouse C, de…
• The Polygenic and Monogenic Basis of Blood Traits and Diseases.
  Cell 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, Wigdor EM, Sakaue S, Moscati A, …
• Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
  Cell 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, Lo KS, Qian H, Lareau CA, Beaudoin M, Hunt …
• The genetics of human hematopoiesis and its disruption in disease.
  EMBO molecular medicine 2019 Bao EL, Cheng AN, Sankaran VG
• Macrothrombocytopenia associated with a rare GFI1B missense variant confounding the presentation of immune thrombocytopenia.
  Pediatric blood & cancer 2019 Cheng AN, Bao EL, Fiorini C, Sankaran VG
• Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis.
  Cell reports 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
• Interrogation of human hematopoiesis at single-cell and single-variant resolution.
  Nature genetics 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
• Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.
  American journal of hematology 2019 Bao EL, Lareau CA, Brugnara C, Fulcher IR, Barau C, Moutereau S, Habibi A, Badaoui B, Berkenou J, Bartolucci P, Galactéros F, Platt OS, Mahaney M, Sankaran VG
• Antiepileptic drug treatment after an unprovoked first seizure: A decision analysis.
  Neurology 2018 Bao EL, Chao LY, Ni P, Moura LMVR, Cole AJ, Cash SS, Hoch DB, Bianchi MT, Westover MB
• Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
  PLoS genetics 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, Young BA, Abecasis GR, Laurie CC, Nickerson DA…
• Dataset on transcriptional profiles and the developmental characteristics of PDGFRα expressing lung fibroblasts.
  Data in brief 2017 Endale M, Ahlfeld S, Bao E, Chen X, Green J, Bess Z, Weirauch M, Xu Y, Perl AK
• SLICE: determining cell differentiation and lineage based on single cell entropy.
  Nucleic acids research 2017 Guo M, Bao EL, Wagner M, Whitsett JA, Xu Y
• Temporal, spatial, and phenotypical changes of PDGFRα expressing fibroblasts during late lung development.
  Developmental biology 2017 Endale M, Ahlfeld S, Bao E, Chen X, Green J, Bess Z, Weirauch MT, Xu Y, Perl AK
• Bronchopulmonary dysplasia impairs L-type amino acid transporter-1 expression in human and baboon lung.
  Pediatric pulmonology 2016 Bao EL, Chystsiakova A, Brahmajothi MV, Sunday ME, Pavlisko EN, Wempe MF, Auten RL
• Persistence of LPS-induced lung inflammation in surfactant protein-C-deficient mice.
  American journal of respiratory cell and molecular biology 2013 Glasser SW, Maxfield MD, Ruetschilling TL, Akinbi HT, Baatz JE, Kitzmiller JA, Page K, Xu Y, Bao EL, Korfhagen TR