Hemmer, Bernhard

  • Bader JM, Makarov C, Richter S, Strauss MT, Held F, Wahle M, Lorenz MB, Pöschl L, Skowronek P, Thielert M, Berthele A, Zeng WF, Ammar C, Bludau I, Schubert B, Theis FJ, Gasperi C, Hemmer B, Mann M. Large-scale proteomics across neurological disorders uncovers biomarker panel and targets in multiple sclerosis. Cell. 2026 Feb 25:S0092-8674(26)00104-2. doi: 10.1016/j.cell.2026.01.017. Epub ahead of print. PMID: 41747728.
  • Braginets A, Oertel FC, Strauß EM, Leutloff C, Schmitz-Hübsch T, Paul F, Asseyer S, Wicklein R, Hemmer B, Ruprecht K, Zimmermann HG, Knier B, Lin TY. Retinal Layer Thickness for Risk Stratification of Progression Independent of Relapse Activity in Relapsing-Remitting Multiple Sclerosis. Brain Behav. 2026 Aug;16(8):e71612. doi: 10.1002/brb3.71612. PMID: 42518178; PMCID: PMC13411297.

  • Corona A, Clarelli F, Pääkkönen K, Harroud A, Shchetynsky K, Zollo A, Mingione A, Sorosina M, Mascia E, Giordano A, Rocca MA, Piehl F, Stridh P, Hemmer B, Goris A, Dubois B, Søndergaard HB, Sellebjerg F, D'alfonso S, Harbo HF, Olsson T, Saarela J, Priori A, Filippi M, Kockum I, Esposito F, Martinelli Boneschi F. Pharmacogenomics of response to interferon-beta and glatiramer acetate in Multiple Sclerosis: A multi-centric study. Mult Scler. 2026 Mar 3:13524585261417130. doi: 10.1177/13524585261417130. Epub ahead of print. PMID: 41776383.

  • Held F, Bayas A, Christe K, Dettmers C, Domurath B, Ebert J, Faßhauer E, Flachenecker P, Gärtner J, Hasanbasic D, Heesen C, Hegen H, Henze T, Huppke P, Kana V, Khalil M, Kirschner-Hermanns R, Korn T, Kümpfel T, Lamprecht S, Meier U, Meyer Zu Horste G, Mäurer M, Oertel FC, Pot C, Pröbstel AK, Rostásy K, Salmen A, Scheiderbauer J, Schmidt M, Stark E, Trebst C, Trollmann R, Warnke C, Wattjes MP, Wiestler B, Wildemann B, Zimmermann U, Gehring K, Berthele A, Hemmer B. Real-world practices and challenges of radiologically isolated syndrome: results of a cross-sector survey by the DACH MS guidelines group. Front Neurol. 2026 Jul 14;17:1822692. doi: 10.3389/fneur.2026.1822692. PMID: 42529218; PMCID: PMC13416845.

  • Hess F, Baki E, McGinnis J, Wiltgen T, Scholz H, Bernkopf K, Schneider G, Kirschke J, Sepp D, Hemmer B, Wunderlich S, Mühlau M. Temporal Patterns of Fever Onset as an Indicator of Etiology in Intracerebral Hemorrhage. Neurol Int. 2026 Apr 3;18(4):68. doi: 10.3390/neurolint18040068. PMID: 42042755; PMCID: PMC13119264.

  • Landt C, Held F, Kolotourou K, Guranda M, Vakrakou AG, Franz J, Thomas C, Schmiedeknecht MUH, Bergann K, Wrzos C, Endmayr V, Tsaktanis T, Zechel S, Ancău M, Misgeld T, Hakroush S, Hametner S, Rothhammer V, Höftberger R, Hemmer B, Stadelmann C, Nessler S. Complement C4d Informs the Differential Diagnosis of Inflammatory Demyelinating CNS Diseases. Neurol Neuroimmunol Neuroinflamm. 2026 Mar;13(2):e200528. doi: 10.1212/NXI.0000000000200528. Epub 2025 Dec 23. PMID: 41435221; PMCID: PMC12735299.
  • Lauerer M, Voon CC, McGinnis J, Sepp D, Meineke J, Wiltgen T, Berg RC, Preibisch C, Wiestler B, Engl C, Uibel P, Berthele A, Kirschke JS, Hemmer B, Mühlau M. The Prognostic Value of Paramagnetic Rim Lesions in People With Multiple Sclerosis. Neurology. 2026 Sep 22;107(6):e218428. doi: 10.1212/WNL.0000000000218428. Epub 2026 Aug 20. PMID: 42623573.

  • Menden B, Incebacak Eltemur RD, Demidov G, Sturm M, Park J, Huridou C, Fath F, Nümann A, Baumann A, Diets IJ, Dufke C, Regensburger M, Rönnefarth M, Wilke V, van Os N, Vielhaber S, Rattay TW, Kohl Z, Peralta S, Pereira Sena P, Kellner M, Weissert N, Traschütz A, Zeltner L, Boelmans K, Deininger N, Schütz L, Gross C, Hinojosa Amaya AB, Raupach K, Hengel H, Harmuth F, Admard J, Bader I, Baumann S, Bender F, Bevot A, Bischoff A, Boschann F, Buchert R, Buchzik D, Casadei N, Catarino CB, Cordts I, Cremer K, Doebler-Neumann M, Ehmke N, Elbracht M, Falb RJ, Feindt T, Fleszar Z, Gerstner L, Gläser D, Grasshoff U, Grosch S, Grundmann K, Gutschalk A, Haaga M, Hayer S, Hehr U, Hellenbroich Y, Henn W, Herr B, Herzog R, Horber V, Deppe J, Kaiser N, Kehrer C, Kehrer M, Kern J, Keßler C, Khuller K, Klinkhammer H, Kotzaeridou U, Krawitz P, Kreiss M, Küpper H, Kuster A, Laugwitz L, Lesemann A, Lichey N, Linden T, Macek B, Magg J, Mangold E, Manka E, Marquardt I, Mehnert K, Mengel D, Morlot S, Oehl-Jaschkowitz B, Pauly MG, Philipp M, Radelfahr F, Rautenberg M, Riess A, Saft C, Schlotter-Weigel B, Schmidt A, Schwaibold EMC, Spahlinger V, Spranger S, Steiner KM, Stendel C, Thieme A, Tzschach A, Velic A, Wiethoff S, Wilke C, Züchner S, Zittel S; Solve-RD consortium; Husain RA, Deschauer M, Distelmaier F, Dufke A, Graessner H, Hemmer B, Jacobi H, Klockgether T, Klopstock T, Kobeleva X, Korenke GC, Kuechler A, Kuhlenbäumer G, Kurth I, Nguyen HP, Wunderlich G, Zeuner KE, Klebe S, Auer-Grumbach M, Butryn M, Winkler J, Timmann D, Synofzik M, van de Warrenburg B, Schüle R, Schöls L, Ossowski S, Riess O, Weber JJ, Haack TB. Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia. Nat Commun. 2026 Feb 14;17(1):1698. doi: 10.1038/s41467-026-69337-9. PMID: 41690933.
  • Nakka P, Hobbs BD, Sidore C, Palmer WH, Murdock D, Gurski L, Glatman Zaretsky A, Moll K, Campos AI, Joshi A, Gaynor SM, Guerreiro R, Kosmicki JA, Tang J, Marcketta A, Baldassari A, Joseph T, Watanabe K, Yu S, Bai X, Gillies CE, Mbatchou J, Sun K, Ganel L, Casullo VM, DiMartino S, Geba GP, Zhang L, Zhu W, Xia Z, Melander O, Chalasani N, Hemmer B, Gasperi C, Held F, Uibel P, Jones M, Shuldiner AR, Balasubramanian S, Ghoussaini M, Ge W, Reid JG, Overton JD, Salerno WJ, Marchini J, Kessler MD, Yancopoulos GD, Orengo JM, Baras A, Lotta LA, Abecasis GR, Siminovitch K, Ferreira MAR; Regeneron Genetics Center; Houston Scleroderma Family Registry and DNA Repository; Consejo Superior de Investigaciones Científicas Study; University of California Los Angeles ATLAS Collaboration; Mayo Clinic Project Generation; GHS-RGC DiscovEHR Collaboration; Colorado Center for Personalized Medicine; Penn Medicine Biobank; Aurora Healthcare System; Mount Sinai Million Health Discoveries Program; Indiana Biobank; Malmö Diet and Cancer Study; University of Tennessee Health Science Center BIG Initiative; Mayo Clinic PBC Cohort; Australia and New Zealand MS Genetics Consortium; Northwestern Scleroderma Patient Registry; Accelerated Cure Project Repository; Technical University of Munich MS Study; University of Pittsburgh PROMOTE Cohort; Oxford Million Women Study; University of Alabama at Birmingham Autoimmune Disease Biorepository; Discover Me South Africa Study. Autoimmune hepatitis and primary biliary cholangitis are among a subset of autoimmune diseases defined by profound co-prevalence and genetic risk association with the IL12 pathway. Hepatology. 2026 Oct 13. doi: 10.1097/HEP.0000000000001819. Epub ahead of print. PMID: 42868031.

  • Oh J, Barkhof F, Bar-Or A, Ciccarrelli O, Coetzee T, Filippi M, Granziera C, Hacohen Y, Hemmer B, Kantarci OH, Kim HJ, Lebrun-Frenay C, Montalban X, Mowry E, Ontaneda D, Prat A, Reich DS, Rovira À, Sati P, Siva A, Solomon AJ, Sormani MP, Stankoff B, Thompson A, Tintore M, Traboulsee A, van der Walt A, Wiendl H, Calabresi PA. Challenges and future directions for multiple sclerosis after the 2024 McDonald diagnostic criteria. Nat Med. 2026 Jul 9. doi: 10.1038/s41591-026-04490-8. Epub ahead of print. PMID: 42426222.

  • Palleis C, Weidinger E, Maaß S, Linke M, Brendel M, Stöcklein S, Al Tawil A, Mansmann U, Teupser D, Borst T, Heimke-Brinck R, Hemmer B, Höglinger GU, Bidner H, Simons M, Levin J. Study protocol: double-blind, randomized, prospective, placebo controlled parallel group phase II study to investigate the effect of glycerol phenylbutyrate (GPB) on neurofilament light chain (NfL) levels in patients with corticobasal syndrome (CBS). Neurol Res Pract. 2026 Jul 3;8(1):54. doi: 10.1186/s42466-026-00504-5. PMID: 42400090; PMCID: PMC13332586.

  • Pretzsch R, El Mahdaoui S, Johnson P, Soares MD, Koerbel K, Held F, Bajrami A, Pozzilli V, Lucchini M, Barbuti E, Bartels F, Barket R, Cordano C, Hemmer B, Cagol A, Schiavetti I, Sormani MP; ECTRIMS Winter School 2024 study group. Neurofilament light chain as a surrogate candidate for disease activity in multiple sclerosis (LUMINOUS)-A meta-regression of randomized controlled trials. Mult Scler. 2026 Jan 23:13524585251407973. doi: 10.1177/13524585251407973. Epub ahead of print. PMID: 41574448.
  • Tahedl M, Wiltgen T, Voon CC, Lauerer M, Kirschke JS, Hemmer B, Mühlau M, Zimmer C, Wiestler B. Brain connectome reorganization across the lifespan in relapsing-remitting multiple sclerosis. Eur J Radiol. 2026 Apr 13;200:112867. doi: 10.1016/j.ejrad.2026.112867. Epub ahead of print. PMID: 41990686.
  • Zeng L, Khan A, Fitzgerald KC, Lama T, Chen J, Li R; International Multiple Sclerosis Genetics Consortium [i.a. Hemmer B]; Tsai EA, Yu K, Chitnis T, Weiner HL, Le Grand Q, Debette S, Wang G, Fujita M, Calabresi PA, Zipp F, Taga M, Kiryluk K, De Jager PL. Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility. Nat Genet. 2026 Sep;58(9):2177-2191. doi: 10.1038/s41588-026-02731-7. Epub 2026 Sep 7. PMID: 42706309.