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Karin E. Finberg, Ph.D. - Publications

Affiliations: 
2002 Yale University, New Haven, CT 
Area:
Genetics
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40 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Li X, Lozovatsky L, Sukumaran A, Gonzalez L, Jain A, Liu D, Ayala-Lopez N, Finberg KE. NCOA4 is Regulated by HIF and Mediates Mobilization of Murine Hepatic Iron Stores After Blood Loss. Blood. PMID 32659785 DOI: 10.1182/Blood.2020006321  0.441
2020 McKnight Q, Jenkins S, Li X, Nelson T, Marlier A, Cantley LG, Finberg KE, Fretz JA. IL-1β drives production of FGF-23 at the onset of chronic kidney disease in mice. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 32154933 DOI: 10.1002/Jbmr.4003  0.351
2019 Finberg KE. Going solo in iron transport. Blood. 134: 1363-1364. PMID 31698431 DOI: 10.1182/Blood.2019003019  0.368
2019 Xavier-Ferrucio J, Scanlon V, Li X, Zhang PX, Lozovatsky L, Ayala-Lopez N, Tebaldi T, Halene S, Cao C, Fleming MD, Finberg KE, Krause DS. Low Iron Promotes Megakaryocytic Commitment of Megakaryocytic-Erythroid Progenitors in Humans and Mice. Blood. PMID 31439541 DOI: 10.1182/Blood.2019002039  0.455
2019 Stagg DB, Whittlesey RL, Li X, Lozovatsky L, Gardenghi S, Rivella S, Finberg KE. Genetic loss of Tmprss6 alters terminal erythroid differentiation in a mouse model of β-thalassemia intermedia. Haematologica. PMID 30819909 DOI: 10.3324/Haematol.2018.213371  0.377
2019 Li X, Lozovatsky L, Finberg KE. NCOA4 Expression in Hepatic Cells Is Upregulated Under Physiological and Pathophysiological Conditions Associated with Hypoxia Blood. 134: 431-431. DOI: 10.1182/Blood-2019-130858  0.414
2018 Stewart T, Finberg K, Walther Z, Sklar JL, Hafez N, Eder JP, Anderson K, Wilson F, Goldberg SB. Yale Cancer Center Precision Medicine Tumor Board: one tumour, multiple targets. The Lancet. Oncology. 19: 1567-1568. PMID 32956641 DOI: 10.1016/S1470-2045(18)30759-9  0.597
2018 Heeney MM, Guo D, De Falco L, Campagna DR, Olbina G, Kao PP, Schmitz-Abe K, Rahimov F, Gutschow P, Westerman K, Ostland V, Jackson T, Klaassen RE, Markianos K, Finberg KE, et al. Normalizing hepcidin predicts mutation status in patients with chronic iron deficiency. Blood. PMID 29895660 DOI: 10.1182/Blood-2017-03-773028  0.431
2018 Li X, Lozovatsky L, Liu D, Ayala-Lopez N, Finberg KE. NCOA4 Mediates Mobilization of Hepatic Iron Stores after Blood Loss Blood. 132: 1046-1046. DOI: 10.1182/Blood-2018-99-119469  0.408
2017 Li X, Lozovatsky L, Sukumaran A, Tommasini S, Fretz JA, Finberg KE. The Tmprss6-/- Mouse Model of Iron Refractory Iron Deficiency Anemia (IRIDA) Exhibits Disrupted Phosphate Homeostasis, Elevated Circulating FGF23 Levels, and Increased Fgf23 Expression in Bone Marrow Blood. 130: 228-228. DOI: 10.1182/Blood.V130.Suppl_1.228.228  0.407
2015 Seid J, Lozovatsky L, Gallagher PG, Finberg KE. Identification of a Novel SLC40A1 Arg88Ile Mutation in a Patient with Familial Iron Overload Treated By Phlebotomy Blood. 126: 954-954. DOI: 10.1182/Blood.V126.23.954.954  0.458
2015 Song Y, Taylor A, Rongvaux A, Jiang T, Podoltsev NA, Xu M, Neparidze N, Torres R, Barbarotta LM, Balasubramanian K, Finberg KE, Kluger Y, Flavell R, Halene S. Efficient Engraftment and Disease Replication of Myelodysplastic Syndromes Using a Novel Humanized Mice Model Blood. 126: 4100-4100. DOI: 10.1182/Blood.V126.23.4100.4100  0.312
2014 Heeney MM, Finberg KE. Iron-refractory iron deficiency anemia (IRIDA). Hematology/Oncology Clinics of North America. 28: 637-52, v. PMID 25064705 DOI: 10.1016/J.Hoc.2014.04.009  0.437
2013 Finberg KE. Striking the target in iron overload disorders. The Journal of Clinical Investigation. 123: 1424-7. PMID 23524962 DOI: 10.1172/Jci68889  0.42
2013 Finberg KE. Regulation of systemic iron homeostasis. Current Opinion in Hematology. 20: 208-14. PMID 23426198 DOI: 10.1097/Moh.0B013E32835F5A47  0.399
2013 Khuong-Quang DA, Schwartzentruber J, Westerman M, Lepage P, Finberg KE, Majewski J, Jabado N. Iron refractory iron deficiency anemia: presentation with hyperferritinemia and response to oral iron therapy. Pediatrics. 131: e620-5. PMID 23319530 DOI: 10.1542/Peds.2012-1303  0.447
2013 Vedovelli L, Rothermel JT, Finberg KE, Wagner CA, Azroyan A, Hill E, Breton S, Brown D, Paunescu TG. Altered V-ATPase expression in renal intercalated cells isolated from B1 subunit-deficient mice by fluorescence-activated cell sorting. American Journal of Physiology. Renal Physiology. 304: F522-32. PMID 23269648 DOI: 10.1152/Ajprenal.00394.2012  0.363
2012 Stagg DB, Gardenghi S, Rivella S, Andrews NC, Finberg KE. Genetic Loss of Tmprss6 Increases Effective Erythropoiesis in a Mouse Model of β-Thalassemia Blood. 120: 482-482. DOI: 10.1182/Blood.V120.21.482.482  0.604
2011 Finberg KE. Unraveling mechanisms regulating systemic iron homeostasis. Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program. 2011: 532-7. PMID 22160085 DOI: 10.1182/Asheducation-2011.1.532  0.427
2011 Finberg KE, Whittlesey RL, Andrews NC. Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice. Blood. 117: 4590-9. PMID 21355094 DOI: 10.1182/Blood-2010-10-315507  0.631
2010 Finberg KE, Whittlesey RL, Fleming MD, Andrews NC. Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis. Blood. 115: 3817-26. PMID 20200349 DOI: 10.1182/Blood-2009-05-224808  0.627
2010 Wehbe RM, Whittlesey RL, Andrews NC, Finberg KE. The Serine Protease Tmprss6 Regulates Hepcidin Expression, but Its Loss Does Not Cause Systemic Iron Deficiency In the Fetal and Neonatal Periods Blood. 116: 4258-4258. DOI: 10.1182/Blood.V116.21.4258.4258  0.615
2010 Finberg KE, Whittlesey RL, Rivella S, Andrews NC. Tmprss6, An Inhibitor of Hepatic Bmp/Smad Signaling, Is Required for Hepcidin Suppression and Iron Loading In a Mouse Model of β-Thalassemia Blood. 116: 164-164. DOI: 10.1182/Blood.V116.21.164.164  0.618
2009 Finberg KE. Iron-refractory iron deficiency anemia. Seminars in Hematology. 46: 378-86. PMID 19786206 DOI: 10.1053/J.Seminhematol.2009.06.006  0.445
2008 Finberg KE. Iron homeostasis: casting new roles. Blood. 112: 2181. PMID 18779402 DOI: 10.1182/Blood-2008-06-164327  0.393
2008 Finberg KE, Heeney MM, Campagna DR, Aydinok Y, Pearson HA, Hartman KR, Mayo MM, Samuel SM, Strouse JJ, Markianos K, Andrews NC, Fleming MD. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nature Genetics. 40: 569-71. PMID 18408718 DOI: 10.1038/Ng.130  0.615
2006 Kovacikova J, Winter C, Loffing-Cueni D, Loffing J, Finberg KE, Lifton RP, Hummler E, Rossier B, Wagner CA. The connecting tubule is the main site of the furosemide-induced urinary acidification by the vacuolar H+-ATPase Kidney International. 70: 1706-1716. PMID 16985514 DOI: 10.1038/Sj.Ki.5001851  0.498
2005 Finberg KE, Wagner CA, Bailey MA, Paunescu TG, Breton S, Brown D, Giebisch G, Geibel JP, Lifton RP. The B1-subunit of the H(+) ATPase is required for maximal urinary acidification. Proceedings of the National Academy of Sciences of the United States of America. 102: 13616-21. PMID 16174750 DOI: 10.1073/Pnas.0506769102  0.521
2005 Nahed BV, Seker A, Guclu B, Ozturk AK, Finberg K, Hawkins AA, DiLuna ML, State M, Lifton RP, Gunel M. Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13. American Journal of Human Genetics. 76: 172-9. PMID 15540160 DOI: 10.1086/426953  0.589
2004 Wagner CA, Finberg KE, Breton S, Marshansky V, Brown D, Geibel JP. Renal vacuolar H+-ATPase. Physiological Reviews. 84: 1263-314. PMID 15383652 DOI: 10.1152/Physrev.00045.2003  0.305
2003 Stehberger PA, Schulz N, Finberg KE, Karet FE, Giebisch G, Lifton RP, Geibel JP, Wagner CA. Localization and Regulation of the ATP6V0A4 (a4) Vacuolar H +-ATPase Subunit Defective in an Inherited Form of Distal Renal Tubular Acidosis Journal of the American Society of Nephrology. 14: 3027-3038. PMID 14638902 DOI: 10.1097/01.Asn.0000099375.74789.Ab  0.497
2003 Finberg KE, Wagner CA, Stehberger PA, Geibel JP, Lifton RP. Molecular cloning and characterization of Atp6v1b1, the murine vacuolar H+-ATPase B1-subunit Gene. 318: 25-34. PMID 14585495 DOI: 10.1016/S0378-1119(03)00790-X  0.509
2003 Dou H, Finberg K, Cardell EL, Lifton R, Choo D. Mice lacking the B1 subunit of H+-ATPase have normal hearing Hearing Research. 180: 76-84. PMID 12782355 DOI: 10.1016/S0378-5955(03)00108-4  0.529
2002 Wagner CA, Finberg KE, Stehberger PA, Lifton RP, Giebisch GH, Aronson PS, Geibel JP. Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status. Kidney International. 62: 2109-17. PMID 12427135 DOI: 10.1046/J.1523-1755.2002.00671.X  0.516
2001 Smith AN, Finberg KE, Wagner CA, Lifton RP, Devonald MA, Su Y, Karet FE. Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene. The Journal of Biological Chemistry. 276: 42382-8. PMID 11495928 DOI: 10.1074/jbc.M107267200  0.413
2001 Cruz DN, Simon DB, Nelson-Williams C, Farhi A, Finberg K, Burleson L, Gill JR, Lifton RP. Mutations in the Na-Cl cotransporter reduce blood pressure in humans. Hypertension (Dallas, Tex. : 1979). 37: 1458-64. PMID 11408395 DOI: 10.1161/01.Hyp.37.6.1458  0.485
1999 Karet FE, Finberg KE, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Medina JF, Lifton RP. Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34. American Journal of Human Genetics. 65: 1656-65. PMID 10577919 DOI: 10.1086/302679  0.513
1999 Karet FE, Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjad SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusunsel R, et al. Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness. Nature Genetics. 21: 84-90. PMID 9916796 DOI: 10.1038/5022  0.528
1996 Günel M, Awad IA, Finberg K, Steinberg GK, Craig HD, Cepeda O, Nelson-Williams C, Lifton RP. Genetic heterogeneity of inherited cerebral cavernous malformation. Neurosurgery. 38: 1265-71. PMID 8727164 DOI: 10.1097/00006123-199606000-00059  0.485
1996 Gunel M, Awad IA, Finberg K, Anson JA, Steinberg GK, Batjer HH, Kopitnik TA, Morrison L, Giannotta SL, Nelson-Williams C, Lifton RP. A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans. The New England Journal of Medicine. 334: 946-51. PMID 8596595 DOI: 10.1056/Nejm199604113341503  0.463
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