Andrea Carmine Belin - Publications

Affiliations: 
Karolinska Institute, Stockholm, Sweden 
Area:
Parkinson genetics

73 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
2021 Jennysdotter Olofsgård F, Ran C, Fourier C, Wirth C, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. Gene Family Polymorphisms in Relation to Cluster Headache and Circadian Rhythm in Sweden. Brain Sciences. 11. PMID 34439727 DOI: 10.3390/brainsci11081108  1
2021 Fourier C, Ran C, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. The molecular clock gene cryptochrome 1 () and its role in cluster headache. Cephalalgia : An International Journal of Headache. 3331024211024165. PMID 34256648 DOI: 10.1177/03331024211024165  1
2021 O'Connor E, Fourier C, Ran C, Sivakumar P, Liesecke F, Southgate L, Harder AVE, Vijfhuizen LS, Yip J, Giffin N, Silver N, Ahmed F, Hostettler IC, Davies B, Cader MZ, ... ... Belin AC, et al. Genome Wide Association Study Identifies Risk Loci For Cluster Headache. Annals of Neurology. PMID 34184781 DOI: 10.1002/ana.26150  1
2020 Ran C, Michalska JM, Fourier C, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. Analysis of NOS Gene Polymorphisms in Relation to Cluster Headache and Predisposing Factors in Sweden. Brain Sciences. 11. PMID 33396232 DOI: 10.3390/brainsci11010034  1
2019 Smedfors G, Liesecke F, Ran C, Olson L, Karlsson TE, Carmine Belin A. Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine. Brain Sciences. 10. PMID 31861860 DOI: 10.3390/Brainsci10010005  0.52
2019 Puschmann A, Jiménez-Ferrer I, Lundblad-Andersson E, Mårtensson E, Hansson O, Odin P, Widner H, Brolin K, Mzezewa R, Kristensen J, Soller M, Rödström EY, Ross OA, Toft M, Breedveld GJ, ... ... Belin AC, et al. Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study. Parkinsonism & Related Disorders. PMID 31422003 DOI: 10.1016/J.Parkreldis.2019.07.032  1
2019 Ran C, Fourier C, Arafa D, Liesecke F, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. Anoctamin 3: A Possible Link between Cluster Headache and Ca Signaling. Brain Sciences. 9. PMID 31366133 DOI: 10.3390/Brainsci9080184  1
2019 Fourier C, Ran C, Steinberg A, Sjöstrand C, Waldenlind E, Belin AC. Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden. Headache. PMID 30652302 DOI: 10.1111/Head.13462  1
2018 Ran C, Fourier C, Zinnegger M, Steinberg A, Sjöstrand C, Waldenlind E, Belin AC. Implications for the migraine SNP rs1835740 in a Swedish cluster headache population. The Journal of Headache and Pain. 19: 100. PMID 30382894 DOI: 10.1186/S10194-018-0937-0  1
2018 Gormley P, Kurki MI, Hiekkala ME, Veerapen K, Häppölä P, Mitchell AA, Lal D, Palta P, Surakka I, Kaunisto MA, Hämäläinen E, Vepsäläinen S, Havanka H, Harno H, Ilmavirta M, ... ... Belin AC, et al. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron. 99: 1098. PMID 30189203 DOI: 10.1016/J.Neuron.2018.08.029  1
2018 Yang Y, Zhao H, Boomsma DI, Ligthart L, Belin AC, Smith GD, Esko T, Freilinger TM, Hansen TF, Ikram MA, Kallela M, Kubisch C, Paraskevi C, Strachan DP, Wessman M, et al. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics : Ejhg. PMID 29995844 DOI: 10.1038/S41431-018-0150-2  1
2018 Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Belin AC, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757  0.68
2018 Gormley P, Kurki MI, Hiekkala ME, Veerapen K, Häppölä P, Mitchell AA, Lal D, Palta P, Surakka I, Kaunisto MA, Hämäläinen E, Vepsäläinen S, Havanka H, Harno H, Ilmavirta M, ... ... Belin AC, et al. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron. PMID 29731251 DOI: 10.1016/J.Neuron.2018.04.014  1
2017 Steinberg A, Fourier C, Ran C, Waldenlind E, Sjöstrand C, Belin AC. Cluster headache - clinical pattern and a new severity scale in a Swedish cohort. Cephalalgia : An International Journal of Headache. 333102417731773. PMID 28906127 DOI: 10.1177/0333102417731773  1
2017 Ran C, Fourier C, Michalska JM, Steinberg A, Sjöstrand C, Waldenlind E, Belin AC. Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort. The Journal of Headache and Pain. 18: 88. PMID 28831700 DOI: 10.1186/S10194-017-0798-Y  1
2017 Ran C, Wirdefeldt K, Brodin L, Ramezani M, Westerlund M, Xiang F, Anvret A, Willows T, Sydow O, Johansson A, Galter D, Svenningsson P, Belin AC. Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease. Parkinson's Disease. 2017: 4020198. PMID 28540099 DOI: 10.1155/2017/4020198  1
2017 Fourier C, Ran C, Zinnegger M, Johansson AS, Sjöstrand C, Waldenlind E, Steinberg A, Belin AC. A genetic CLOCK variant associated with cluster headache causing increased mRNA levels. Cephalalgia : An International Journal of Headache. 333102417698709. PMID 28466652 DOI: 10.1177/0333102417698709  1
2016 Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Belin AC, et al. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. 48: 1296. PMID 27681292 DOI: 10.1038/Ng1016-1296C  1
2016 Ran C, Mehdi RN, Fardell C, Xiang F, Nissbrandt H, Sydow O, Wirdefeldt K, Belin AC. No Association Between rs7077361 in ITGA8 and Parkinson's Disease in Sweden. The Open Neurology Journal. 10: 25-9. PMID 27583043 DOI: 10.2174/1874205X01610010025  1
2016 Aguilar-Roblero R, Quinto D, Báez-Ruíz A, Chávez JL, Belin AC, Díaz-Muñoz M, Michel S, Lundkvist G. Ryanodine-sensitive intracellular ca(2+) channels are involved in the output from the scn circadian clock. The European Journal of Neuroscience. PMID 27529310 DOI: 10.1111/Ejn.13368  0.01
2016 Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Belin AC, et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. PMID 27322543 DOI: 10.1038/Ng.3598  0.68
2016 Ran C, Brodin L, Forsgren L, Westerlund M, Ramezani M, Gellhaar S, Xiang F, Fardell C, Nissbrandt H, Söderkvist P, Puschmann A, Ygland E, Olson L, Willows T, Johansson A, ... ... Belin AC, et al. Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden. Neurobiology of Aging. PMID 27255555 DOI: 10.1016/J.Neurobiolaging.2016.04.022  1
2015 Graae L, Paddock S, Belin AC. ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide. Genetics Research. 97: e8. PMID 25882789 DOI: 10.1017/S0016672315000051  1
2015 Stefaniu C, Zaffalon PL, Carmine A, Verolet Q, Fernandez S, Wesolowski TA, Brezesinski G, Zumbuehl A. Rigid urea and self-healing thiourea ethanolamine monolayers. Langmuir : the Acs Journal of Surfaces and Colloids. 31: 1296-302. PMID 25594235 DOI: 10.1021/la5039987  0.68
2014 Stefano C, Giuseppe del T, Romano M, Carmine A. Primary Bilateral Extramammary Paget's Disease of the Axillae: Another Case of this Strange Disease. Journal of Cutaneous and Aesthetic Surgery. 7: 131-4. PMID 25136219 DOI: 10.4103/0974-2077.138365  0.68
2014 Ran C, Graae L, Magnusson PK, Pedersen NL, Olson L, Belin AC. A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample. Bmc Medical Genetics. 15: 38. PMID 24674449 DOI: 10.1186/1471-2350-15-38  1
2013 Carmine A, Domoto Y, Sakai N, Matile S. Comparison of lipoic and asparagusic acid for surface-initiated disulfide-exchange polymerization. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 11558-63. PMID 23893874 DOI: 10.1002/Chem.201301567  0.68
2013 Ran C, Willows T, Sydow O, Johansson A, Söderkvist P, Dizdar N, Ahmadi A, Olson L, Belin AC. The HLA-DRA variation rs3129882 is not associated with Parkinson's disease in Sweden. Parkinsonism & Related Disorders. 19: 701-2. PMID 23579001 DOI: 10.1016/J.Parkreldis.2013.03.001  1
2012 Belin AC, Ran C, Anvret A, Paddock S, Westerlund M, HÃ¥kansson A, Nissbrandt H, Söderkvist P, Dizdar N, Ahmadi A, Anvret M, Willows T, Sydow O, Galter D. Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease. Neuroscience Letters. 522: 30-5. PMID 22704918 DOI: 10.1016/J.Neulet.2012.06.007  1
2012 Anvret A, Ran C, Westerlund M, Sydow O, Willows T, Olson L, Galter D, Belin AC. Genetic Screening of the Mitochondrial Rho GTPases MIRO1 and MIRO2 in Parkinson's Disease. The Open Neurology Journal. 6: 1-5. PMID 22496713 DOI: 10.2174/1874205X01206010001  1
2012 Karlsson R, Graae L, Lekman M, Wang D, Favis R, Axelsson T, Galter D, Belin AC, Paddock S. MAGI1 copy number variation in bipolar affective disorder and schizophrenia. Biological Psychiatry. 71: 922-30. PMID 22381734 DOI: 10.1016/J.Biopsych.2012.01.020  0.76
2012 Anvret A, Ran C, Westerlund M, Gellhaar S, Lindqvist E, Pernold K, Lundströmer K, Duester G, Felder MR, Galter D, Belin AC. Adh1 and Adh1/4 knockout mice as possible rodent models for presymptomatic Parkinson's disease. Behavioural Brain Research. 227: 252-7. PMID 22079585 DOI: 10.1016/J.Bbr.2011.10.040  1
2011 Ran C, Westerlund M, Anvret A, Willows T, Sydow O, Galter D, Belin AC. Genetic studies of the protein kinase AKT1 in Parkinson's disease. Neuroscience Letters. 501: 41-4. PMID 21741444 DOI: 10.1016/J.Neulet.2011.06.038  1
2011 Anvret A, Blackinton JG, Westerlund M, Ran C, Sydow O, Willows T, Håkansson A, Nissbrandt H, Belin AC. DJ-1 Mutations are Rare in a Swedish Parkinson Cohort. The Open Neurology Journal. 5: 8-11. PMID 21532868 DOI: 10.2174/1874205X01105010008  1
2011 Westerlund M, Behbahani H, Gellhaar S, Forsell C, Belin AC, Anvret A, Zettergren A, Nissbrandt H, Lind C, Sydow O, Graff C, Olson L, Ankarcrona M, Galter D. Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1345-52. PMID 21163861 DOI: 10.1096/Fj.10-163402  1
2011 Belin AC, Westerlund M, Anvret A, Lindqvist E, Pernold K, Ogren SO, Duester G, Galter D. Modeling Parkinson's disease genetics: altered function of the dopamine system in Adh4 knockout mice. Behavioural Brain Research. 217: 439-45. PMID 21075145 DOI: 10.1016/J.Bbr.2010.11.023  1
2010 Anvret A, Ran C, Westerlund M, Thelander AC, Sydow O, Lind C, Håkansson A, Nissbrandt H, Galter D, Belin AC. Possible involvement of a mitochondrial translation initiation factor 3 variant causing decreased mRNA levels in Parkinson's disease. Parkinson's Disease. 2010: 491751. PMID 20976088 DOI: 10.4061/2010/491751  1
2010 Anvret A, Westerlund M, Sydow O, Willows T, Lind C, Galter D, Belin AC. Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden. Neuroscience Letters. 485: 117-20. PMID 20826197 DOI: 10.1016/J.Neulet.2010.08.082  1
2010 Bergman O, HÃ¥kansson A, Westberg L, Nordenström K, Carmine Belin A, Sydow O, Olson L, Holmberg B, Eriksson E, Nissbrandt H. PITX3 polymorphism is associated with early onset Parkinson's disease. Neurobiology of Aging. 31: 114-7. PMID 18420308 DOI: 10.1016/J.Neurobiolaging.2008.03.008  0.76
2009 Shahabi HN, Westberg L, Melke J, HÃ¥kansson A, Belin AC, Sydow O, Olson L, Holmberg B, Nissbrandt H. Cytochrome P450 2E1 gene polymorphisms/haplotypes and Parkinson's disease in a Swedish population. Journal of Neural Transmission (Vienna, Austria : 1996). 116: 567-73. PMID 19381774 DOI: 10.1007/s00702-009-0221-1  1
2009 Westerlund M, Belin AC, Anvret A, HÃ¥kansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Association of a polymorphism in the ABCB1 gene with Parkinson's disease. Parkinsonism & Related Disorders. 15: 422-4. PMID 19196542 DOI: 10.1016/J.Parkreldis.2008.11.010  1
2009 Bergman O, HÃ¥kansson A, Westberg L, Belin AC, Sydow O, Olson L, Holmberg B, Fratiglioni L, Bäckman L, Eriksson E, Nissbrandt H. Do polymorphisms in transcription factors LMX1A and LMX1B influence the risk for Parkinson's disease? Journal of Neural Transmission (Vienna, Austria : 1996). 116: 333-8. PMID 19189040 DOI: 10.1007/S00702-009-0187-Z  1
2008 Westerlund M, Belin AC, Olson L, Galter D. Expression of multi-drug resistance 1 mRNA in human and rodent tissues: reduced levels in Parkinson patients. Cell and Tissue Research. 334: 179-85. PMID 18855017 DOI: 10.1007/S00441-008-0686-5  1
2008 Westerlund M, Belin AC, Anvret A, HÃ¥kansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 22: 3509-14. PMID 18606870 DOI: 10.1096/Fj.08-110148  1
2008 HÃ¥kansson A, Belin AC, Stiller C, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Investigation of genes related to familial forms of Parkinson's disease--with focus on the Parkin gene. Parkinsonism & Related Disorders. 14: 520-2. PMID 18321758 DOI: 10.1016/J.Parkreldis.2007.10.013  1
2008 Belin AC, Westerlund M. Parkinson's disease: a genetic perspective. The Febs Journal. 275: 1377-83. PMID 18279377 DOI: 10.1111/J.1742-4658.2008.06301.X  1
2008 Westerlund M, Belin AC, Anvret A, Bickford P, Olson L, Galter D. Developmental regulation of leucine-rich repeat kinase 1 and 2 expression in the brain and other rodent and human organs: Implications for Parkinson's disease. Neuroscience. 152: 429-36. PMID 18272292 DOI: 10.1016/J.Neuroscience.2007.10.062  1
2008 Belin AC, Galter D. S18Y, UCH-L1 and Parkinson’s Disease European Neurological Review. 3: 41. DOI: 10.17925/Enr.2008.03.02.41  1
2008 Håkansson A, Bergman O, Chrapkowska C, Westberg L, Belin AC, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Cyclooxygenase-2 polymorphisms in Parkinson's disease (American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 144B, (367-369)) American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147: 541. DOI: 10.1002/ajmg.b.30790  1
2007 Galter D, Westerlund M, Belin AC, Olson L. DJ-1 and UCH-L1 gene activity patterns in the brains of controls, Parkinson and schizophrenia patients and in rodents. Physiology & Behavior. 92: 46-53. PMID 17599367 DOI: 10.1016/J.Physbeh.2007.05.046  1
2007 Belin AC, Björk BF, Westerlund M, Galter D, Sydow O, Lind C, Pernold K, Rosvall L, HÃ¥kansson A, Winblad B, Nissbrandt H, Graff C, Olson L. Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease. Neuroscience Letters. 420: 257-62. PMID 17537576 DOI: 10.1016/J.Neulet.2007.05.010  1
2007 Carmine Belin A, Westerlund M, Bergman O, Nissbrandt H, Lind C, Sydow O, Galter D. S18Y in ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) associated with decreased risk of Parkinson's disease in Sweden. Parkinsonism & Related Disorders. 13: 295-8. PMID 17287139 DOI: 10.1016/J.Parkreldis.2006.12.002  0.76
2007 Westerlund M, Belin AC, Felder MR, Olson L, Galter D. High and complementary expression patterns of alcohol and aldehyde dehydrogenases in the gastrointestinal tract: implications for Parkinson's disease. The Febs Journal. 274: 1212-23. PMID 17257171 DOI: 10.1111/J.1742-4658.2007.05665.X  1
2007 HÃ¥kansson A, Bergman O, Chrapkowska C, Westberg L, Belin AC, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Cyclooxygenase-2 polymorphisms in Parkinson's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 367-9. PMID 17171651 DOI: 10.1002/Ajmg.B.30449  1
2006 Carmine Belin A, Westerlund M, Sydow O, Lundströmer K, HÃ¥kansson A, Nissbrandt H, Olson L, Galter D. Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish Parkinson cohort and a healthy nonagenarian. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 1731-4. PMID 16817197 DOI: 10.1002/Mds.21016  1
2006 Galter D, Westerlund M, Carmine A, Lindqvist E, Sydow O, Olson L. LRRK2 expression linked to dopamine-innervated areas. Annals of Neurology. 59: 714-9. PMID 16532471 DOI: 10.1002/ana.20808  0.76
2005 Westerlund M, Galter D, Carmine A, Olson L. Tissue- and species-specific expression patterns of class I, III, and IV Adh and Aldh 1 mRNAs in rodent embryos. Cell and Tissue Research. 322: 227-36. PMID 16047160 DOI: 10.1007/s00441-005-0038-7  0.76
2005 HÃ¥kansson A, Westberg L, Nilsson S, Buervenich S, Carmine A, Holmberg B, Sydow O, Olson L, Johnels B, Eriksson E, Nissbrandt H. Investigation of genes coding for inflammatory components in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 569-73. PMID 15648059 DOI: 10.1002/mds.20378  0.76
2005 Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, et al. A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. Archives of Neurology. 62: 74-8. PMID 15642852 DOI: 10.1001/Archneur.62.1.74  0.76
2005 HÃ¥kansson A, Westberg L, Nilsson S, Buervenich S, Carmine A, Holmberg B, Sydow O, Olson L, Johnels B, Eriksson E, Nissbrandt H. Interaction of polymorphisms in the genes encoding interleukin-6 and estrogen receptor beta on the susceptibility to Parkinson's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 133: 88-92. PMID 15635591 DOI: 10.1002/ajmg.b.30136  0.76
2004 Westberg L, HÃ¥kansson A, Melke J, Shahabi HN, Nilsson S, Buervenich S, Carmine A, Ahlberg J, Grundell MB, Schulhof B, Klingborg K, Holmberg B, Sydow O, Olson L, Johnels EB, et al. Association between the estrogen receptor beta gene and age of onset of Parkinson's disease. Psychoneuroendocrinology. 29: 993-8. PMID 15219649 DOI: 10.1016/j.psyneuen.2003.08.010  0.76
2003 Galter D, Buervenich S, Carmine A, Anvret M, Olson L. ALDH1 mRNA: presence in human dopamine neurons and decreases in substantia nigra in Parkinson's disease and in the ventral tegmental area in schizophrenia. Neurobiology of Disease. 14: 637-47. PMID 14678778  0.76
2003 Carmine A, Buervenich S, Galter D, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Chowdari KV, Nimgaonkar VL, Anvret M, Sydow O, Olson L. NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 120: 51-7. PMID 12815740 DOI: 10.1002/Ajmg.B.20033  0.76
2003 Werme M, Hermanson E, Carmine A, Buervenich S, Zetterström RH, Thorén P, Ogren SO, Olson L, Perlmann T, Brené S. Decreased ethanol preference and wheel running in Nurr1-deficient mice. The European Journal of Neuroscience. 17: 2418-24. PMID 12814373 DOI: 10.1046/j.1460-9568.2003.02666.x  0.76
2003 HÃ¥kansson A, Melke J, Westberg L, Shahabi HN, Buervenich S, Carmine A, Klingborg K, Grundell MB, Schulhof B, Holmberg B, Ahlberg J, Eriksson E, Sydow O, Olson L, Johnels B, et al. Lack of association between the BDNF Val66Met polymorphism and Parkinson's disease in a Swedish population. Annals of Neurology. 53: 823. PMID 12783434 DOI: 10.1002/ana.10585  0.76
2003 Galter D, Carmine A, Buervenich S, Duester G, Olson L. Distribution of class I, III and IV alcohol dehydrogenase mRNAs in the adult rat, mouse and human brain. European Journal of Biochemistry / Febs. 270: 1316-26. PMID 12631290  0.76
2003 Carmine A, Chheda MG, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Anvret M, Buervenich S, Olson L. Two NOTCH4 polymorphisms and their relation to schizophrenia susceptibility and different personality traits. Psychiatric Genetics. 13: 23-8. PMID 12605097 DOI: 10.1097/01.ypg.0000056680.82896.22  0.76
2002 Carmine A, Buervenich S, Sydow O, Anvret M, Olson L. Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 17: 764-6. PMID 12210872 DOI: 10.1002/mds.10172  0.76
2000 Buervenich S, Carmine A, Arvidsson M, Xiang F, Zhang Z, Sydow O, Jönsson EG, Sedvall GC, Leonard S, Ross RG, Freedman R, Chowdari KV, Nimgaonkar VL, Perlmann T, Anvret M, et al. NURR1 mutations in cases of schizophrenia and manic-depressive disorder. American Journal of Medical Genetics. 96: 808-13. PMID 11121187 DOI: 10.1002/1096-8628(20001204)96:6<808::Aid-Ajmg23>3.0.Co;2-E  0.76
2000 Buervenich S, Sydow O, Carmine A, Zhang Z, Anvret M, Olson L. Alcohol dehydrogenase alleles in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 15: 813-8. PMID 11009184 DOI: 10.1002/1531-8257(200009)15:5<813::AID-MDS1008>3.0.CO;2-Y  0.76
1982 Heel RC, Brogden RN, Carmine A, Morley PA, Speight TM, Avery GS. Ketoconazole: a review of its therapeutic efficacy in superficial and systemic fungal infections. Drugs. 23: 1-36. PMID 6276122  0.68
1981 Brogden RN, Carmine A, Heel RC, Morley PA, Speight TM, Avery GS. Amoxycillin/clavulanic acid: a review of its antibacterial activity, pharmacokinetics and therapeutic use. Drugs. 22: 337-62. PMID 7037354  0.68
1981 Brogden RN, Carmine A, Heel RC, Morley PA, Speight TM, Avery GS. Cefoperazone: A review of its in vitro antimicrobial activity, pharmacological properties and therapeutic efficacy. Drugs. 22: 423-60. PMID 6459224  0.68
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