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Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke.
Brain. 2022 Jul 29;145(7):2394-2406. doi: 10.1093/brain/awac080.
Brain. 2022.
PMID: 35213696
Free PMC article.
Early Neurological Change After Ischemic Stroke Is Associated With 90-Day Outcome.
Heitsch L, Ibanez L, Carrera C, Binkley MM, Strbian D, Tatlisumak T, Bustamante A, Ribó M, Molina C, Dávalos A, López-Cancio E, Muñoz-Narbona L, Soriano-Tárraga C, Giralt-Steinhauer E, Obach V, Slowik A, Pera J, Lapicka-Bodzioch K, Derbisz J, Sobrino T, Castillo J, Campos F, Rodríguez-Castro E, Arias-Rivas S, Segura T, Serrano-Heras G, Vives-Bauza C, Díaz-Navarro R, Tur S, Jimenez C, Martí-Fàbregas J, Delgado-Mederos R, Arenillas J, Krupinski J, Cullell N, Torres-Aguila NP, Muiño E, Cárcel-Márquez J, Moniche F, Cabezas JA, Ford AL, Dhar R, Roquer J, Khatri P, Jiménez-Conde J, Fernandez-Cadenas I, Montaner J, Rosand J, Cruchaga C, Lee JM; International Stroke Genetics Consortium.
Heitsch L, et al. Among authors: lapicka bodzioch k.
Stroke. 2021 Jan;52(1):132-141. doi: 10.1161/STROKEAHA.119.028687. Epub 2020 Dec 15.
Stroke. 2021.
PMID: 33317415
Free PMC article.
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Multi-ancestry genetic study in 5,876 patients identifies an association between excitotoxic genes and early outcomes after acute ischemic stroke.
Ibanez L, Heitsch L, Carrera C, Farias FHG, Dhar R, Budde J, Bergmann K, Bradley J, Harari O, Phuah CL, Lemmens R, Souza AAVO, Moniche F, Cabezas-Juan A, Arenillas JF, Krupinksi J, Cullell N, Torres-Aguila N, Muiño E, Cárcel-Márquez J, Marti-Fabregas J, Delgado-Mederos R, Marin-Bueno R, Hornick A, Vives-Bauza C, Navarro RD, Tur S, Jimenez C, Obach V, Segura T, Serrano-Heras G, Chung JW, Roquer J, Soriano-Tarraga C, Giralt-Steinhauer E, Mola-Caminal M, Pera J, Lapicka-Bodzioch K, Derbisz J, Davalos A, Lopez-Cancio E, Muñoz L, Tatlisumak T, Molina C, Ribo M, Bustamante A, Sobrino T, Castillo-Sanchez J, Campos F, Rodriguez-Castro E, Arias-Rivas S, Rodríguez-Yáñez M, Herbosa C, Ford AL, Arauz A, Lopes-Cendes I, Lowenkopf T, Barboza MA, Amini H, Stamova B, Ander BP, Sharp FR, Kim GM, Bang OY, Jimenez-Conde J, Slowik A, Stribian D, Tsai EA, Burkly LC, Montaner J, Fernandez-Cadenas I, Lee JM, Cruchaga C.
Ibanez L, et al. Among authors: lapicka bodzioch k.
medRxiv [Preprint]. 2020 Nov 3:2020.10.29.20222257. doi: 10.1101/2020.10.29.20222257.
medRxiv. 2020.
PMID: 33173895
Free PMC article.
Updated.
Preprint.
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Severe dystonic encephalopathy without hyperphenylalaninemia associated with an 18-bp deletion within the proximal GCH1 promoter.
Bodzioch M, Lapicka-Bodzioch K, Rudzinska M, Pietrzyk JJ, Bik-Multanowski M, Szczudlik A.
Bodzioch M, et al. Among authors: lapicka bodzioch k.
Mov Disord. 2011 Feb 1;26(2):337-40. doi: 10.1002/mds.23364. Epub 2010 Sep 14.
Mov Disord. 2011.
PMID: 20842687
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Evidence for potential functionality of nuclearly-encoded humanin isoforms.
Bodzioch M, Lapicka-Bodzioch K, Zapala B, Kamysz W, Kiec-Wilk B, Dembinska-Kiec A.
Bodzioch M, et al. Among authors: lapicka bodzioch k.
Genomics. 2009 Oct;94(4):247-56. doi: 10.1016/j.ygeno.2009.05.006. Epub 2009 May 27.
Genomics. 2009.
PMID: 19477263
Free article.
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The microarray expression analysis identifies BAX as a mediator of beta-carotene effects on apoptosis.
Bodzioch M, Dembinska-Kiec A, Hartwich J, Lapicka-Bodzioch K, Banas A, Polus A, Grzybowska J, Wybranska I, Dulinska J, Gil D, Laidler P, Placha W, Zawada M, Balana-Nowak A, Sacha T, Kiec-Wilk B, Skotnicki A, Moehle C, Langmann T, Schmitz G.
Bodzioch M, et al. Among authors: lapicka bodzioch k.
Nutr Cancer. 2005;51(2):226-35. doi: 10.1207/s15327914nc5102_13.
Nutr Cancer. 2005.
PMID: 15860445
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Expression pattern and raft association of NIPSNAP3 and NIPSNAP4, highly homologous proteins encoded by genes in close proximity to the ATP-binding cassette transporter A1.
Buechler C, Bodzioch M, Bared SM, Sigruener A, Boettcher A, Lapicka-Bodzioch K, Aslanidis C, Duong CQ, Grandl M, Langmann T, Dembinska-Kiec A, Schmitz G.
Buechler C, et al. Among authors: lapicka bodzioch k.
Genomics. 2004 Jun;83(6):1116-24. doi: 10.1016/j.ygeno.2003.12.011.
Genomics. 2004.
PMID: 15177564
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Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome.
Lapicka-Bodzioch K, Bodzioch M, Krüll M, Kielar D, Probst M, Kiec B, Andrikovics H, Böttcher A, Hubacek J, Aslanidis C, Suttorp N, Schmitz G.
Lapicka-Bodzioch K, et al.
Biochim Biophys Acta. 2001 Jul 27;1537(1):42-8. doi: 10.1016/s0925-4439(01)00053-9.
Biochim Biophys Acta. 2001.
PMID: 11476961
Free article.
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