Harvard Catalyst Profiles

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Jakob Hoeppner, M.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Höppner J, Casteleyn V, Biesen R, Rose T, Windisch W, Burmester GR, Siegert E. SIGLEC-1 in Systemic Sclerosis: A Useful Biomarker for Differential Diagnosis. Pharmaceuticals (Basel). 2022 Sep 28; 15(10). PMID: 36297311; PMCID: PMC9610402.
  2. Höppner J, Bruni C, Distler O, Robson SC, Burmester GR, Siegert E, Distler JHW. Purinergic signalling in systemic sclerosis. Rheumatology (Oxford). 2022 07 06; 61(7):2770-2782. PMID: 34849624.
    Citations:    Fields:    Translation:HumansCells
  3. Tabeling C, González Calera CR, Lienau J, Höppner J, Tschernig T, Kershaw O, Gutbier B, Naujoks J, Herbert J, Opitz B, Gruber AD, Hocher B, Suttorp N, Heidecke H, Burmester GR, Riemekasten G, Siegert E, Kuebler WM, Witzenrath M. Endothelin B Receptor Immunodynamics in Pulmonary Arterial Hypertension. Front Immunol. 2022; 13:895501. PMID: 35757687; PMCID: PMC9221837.
    Citations:    Fields:    Translation:HumansAnimals
  4. Höppner J, Sinningen K, Raimann A, Obermayer-Pietsch B, Grasemann C. Disorders of the Calcium Sensing Signaling Pathway: From Familial Hypocalciuric Hypercalcemia (FHH) to Life Threatening Conditions in Infancy. J Clin Med. 2022 May 05; 11(9). PMID: 35566721; PMCID: PMC9100033.
    Citations: 1     
  5. Höppner J, Lais S, Roll C, Wegener-Panzer A, Wieczorek D, Högler W, Grasemann C. Case Report: Severe Neonatal Course in Paternally Derived Familial Hypocalciuric Hypercalcemia. Front Endocrinol (Lausanne). 2021; 12:700612. PMID: 34659108; PMCID: PMC8518617.
    Citations: 2     Fields:    Translation:Humans
  6. Schündeln MM, Höppner J, Meyer FL, Schmuck W, Kauther MD, Hilken G, Levkau B, Rauner M, Grasemann C. Prednisone prevents particle induced bone loss in the calvaria mouse model. Heliyon. 2021 Aug; 7(8):e07828. PMID: 34471710; PMCID: PMC8387912.
    Citations: 1     
  7. Höppner J, Steff K, Lobert F, Heyer CM, Hauffa BP, Grasemann C. Rhizomelia and Impaired Linear Growth in a Girl with Juvenile Paget Disease: The Natural History of the Condition. Horm Res Paediatr. 2021; 94(3-4):151-158. PMID: 34261073.
    Citations:    Fields:    Translation:Humans
  8. Höppner J, Kornak U, Sinningen K, Rutsch F, Oheim R, Grasemann C. Autosomal recessive hypophosphatemic rickets type 2 (ARHR2) due to ENPP1-deficiency. Bone. 2021 12; 153:116111. PMID: 34252603.
    Citations: 4     Fields:    Translation:Humans
  9. Siegert E, Uruha A, Goebel HH, Preuße C, Casteleyn V, Kleefeld F, Alten R, Burmester GR, Schneider U, Höppner J, Hahn K, Dittmayer C, Stenzel W. Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology. Acta Neuropathol. 2021 06; 141(6):917-927. PMID: 33864496; PMCID: PMC8113184.
    Citations: 5     Fields:    Translation:Humans
  10. Höppner J, Steff K, Misof BM, Schündeln MM, Hövel M, Lücke T, Grasemann C. Clinical course in two children with Juvenile Paget's disease during long-term treatment with intravenous bisphosphonates. Bone Rep. 2021 Jun; 14:100762. PMID: 33850973; PMCID: PMC8039828.
  11. March C, Huscher D, Preis E, Makowka A, Hoeppner J, Buttgereit F, Riemekasten G, Norman K, Siegert E. Response to the Letter to the Editor: Prevalence, Risk Factors and Assessment of Depressive Symptoms in Patients With Systemic Sclerosis. Arch Rheumatol. 2020 Sep; 35(3):460-461. PMID: 33458675; PMCID: PMC7788653.
  12. Casteleyn V, Höppner J. Recurring Fever. Dtsch Arztebl Int. 2019 02 22; 116(8):134. PMID: 30940343; PMCID: PMC6454806.
    Citations:    Fields:    Translation:Humans
  13. March C, Huscher D, Preis E, Makowka A, Hoeppner J, Buttgereit F, Riemekasten G, Norman K, Siegert E. Prevalence, Risk Factors and Assessment of Depressive Symptoms in Patients With Systemic Sclerosis. Arch Rheumatol. 2019 09; 34(3):253-261. PMID: 31598589; PMCID: PMC6768792.
    Citations: 5     
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.