Ben Oostra - Publications

Affiliations: 
Erasmus Medical Center Rotterdam, Rotterdam, Netherlands 

225 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
2019 Karasik D, Zillikens MC, Hsu YH, Aghdassi A, Akesson K, Amin N, Barroso I, Bennett DA, Bertram L, Bochud M, Borecki IB, Broer L, Buchman AS, Byberg L, Campbell H, ... ... Oostra BA, et al. Disentangling the genetics of lean mass. The American Journal of Clinical Nutrition. PMID 30721968 DOI: 10.1093/Ajcn/Nqy272  0.4
2018 Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Oostra BA, et al. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30429575 DOI: 10.1038/S41588-018-0297-3  0.36
2018 Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Oostra BA, et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30224653 DOI: 10.1038/S41588-018-0205-X  0.36
2018 Silva CT, Zorkoltseva IV, Niemeijer MN, van den Berg ME, Amin N, Demirkan A, van Leeuwen E, Iglesias AI, Piñeros-Hernández LB, Restrepo CM, Kors JA, Kirichenko AV, Willemsen R, Oostra BA, Stricker BH, et al. A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy. Bmc Medical Genomics. 11: 22. PMID 29506515 DOI: 10.1186/s12920-018-0339-9  0.4
2017 Zillikens MC, Demissie S, Hsu YH, Yerges-Armstrong LM, Chou WC, Stolk L, Livshits G, Broer L, Johnson T, Koller DL, Kutalik Z, Luan J, Malkin I, Ried JS, Smith AV, ... ... Oostra BA, et al. Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nature Communications. 8: 1414. PMID 29116125 DOI: 10.1038/s41467-017-01008-2  0.4
2017 Zillikens MC, Demissie S, Hsu YH, Yerges-Armstrong LM, Chou WC, Stolk L, Livshits G, Broer L, Johnson T, Koller DL, Kutalik Z, Luan J, Malkin I, Ried JS, Smith AV, ... ... Oostra BA, et al. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nature Communications. 8: 80. PMID 28724990 DOI: 10.1038/S41467-017-00031-7  0.4
2017 Springelkamp H, Iglesias AI, Mishra A, Höhn R, Wojciechowski R, Khawaja AP, Nag A, Wang YX, Wang JJ, Cuellar-Partida G, Gibson J, Cooke Bailey JN, Vithana EN, Gharahkhani P, Boutin T, ... ... Oostra BA, et al. New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Human Molecular Genetics. PMID 28073927 DOI: 10.1093/Hmg/Ddw399  0.36
2016 Silva CT, Zorkoltseva IV, Amin N, Demirkan A, van Leeuwen EM, Kors JA, van den Berg M, Stricker BH, Uitterlinden AG, Kirichenko AV, Witteman JC, Willemsen R, Oostra BA, Axenovich TI, van Duijn CM, et al. A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study. Frontiers in Genetics. 7: 190. PMID 27877193 DOI: 10.3389/fgene.2016.00190  0.4
2016 Amin N, Allebrandt KV, van der Spek A, Müller-Myhsok B, Hek K, Teder-Laving M, Hayward C, Esko T, van Mill JG, Mbarek H, Watson NF, Melville SA, Del Greco FM, Byrne EM, Oole E, ... ... Oostra BA, et al. Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics : Ejhg. PMID 27142678 DOI: 10.1038/Ejhg.2016.31  0.56
2015 Silva CT, Kors JA, Amin N, Dehghan A, Witteman JC, Willemsen R, Oostra BA, van Duijn CM, Isaacs A. Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval. Human Genetics. PMID 26385552 DOI: 10.1007/s00439-015-1595-9  0.56
2015 van Leeuwen EM, Karssen LC, Deelen J, Isaacs A, Medina-Gomez C, Mbarek H, Kanterakis A, Trompet S, Postmus I, Verweij N, van Enckevort DJ, Huffman JE, White CC, Feitosa MF, Bartz TM, ... ... Oostra BA, et al. Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Nature Communications. 6: 6065. PMID 25751400 DOI: 10.1038/Ncomms7065  0.4
2015 Verhaaren BF, Debette S, Bis JC, Smith JA, Ikram MK, Adams HH, Beecham AH, Rajan KB, Lopez LM, Barral S, van Buchem MA, van der Grond J, Smith AV, Hegenscheid K, Aggarwal NT, ... ... Oostra BA, et al. Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI. Circulation. Cardiovascular Genetics. 8: 398-409. PMID 25663218 DOI: 10.1161/Circgenetics.114.000858  0.56
2015 Debette S, Ibrahim Verbaas CA, Bressler J, Schuur M, Smith A, Bis JC, Davies G, Wolf C, Gudnason V, Chibnik LB, Yang Q, deStefano AL, de Quervain DJ, Srikanth V, Lahti J, ... ... Oostra B, et al. Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. Biological Psychiatry. 77: 749-63. PMID 25648963 DOI: 10.1016/J.Biopsych.2014.08.027  0.56
2015 Springelkamp H, Mishra A, Hysi PG, Gharahkhani P, Höhn R, Khor CC, Cooke Bailey JN, Luo X, Ramdas WD, Vithana E, Koh V, Yazar S, Xu L, Forward H, Kearns LS, ... ... Oostra BA, et al. Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Genetic Epidemiology. 39: 207-16. PMID 25631615 DOI: 10.1002/Gepi.21886  0.56
2015 Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, Höhn R, Vitart V, Hewitt AW, Oexle K, Mäkelä KM, MacGregor S, Pirastu M, Fan Q, Cheng CY, ... ... Oostra BA, et al. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics. 134: 131-46. PMID 25367360 DOI: 10.1007/S00439-014-1500-Y  0.56
2015 Quadri M, Yang X, Cossu G, Olgiati S, Saddi VM, Breedveld GJ, Ouyang L, Hu J, Xu N, Graafland J, Ricchi V, Murgia D, Guedes LC, Mariani C, Marti MJ, ... ... Oostra BA, et al. An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate. Neurogenetics. 16: 55-64. PMID 25294124 DOI: 10.1007/s10048-014-0425-x  0.56
2015 Cornelis MC, Byrne EM, Esko T, Nalls MA, Ganna A, Paynter N, Monda KL, Amin N, Fischer K, Renstrom F, Ngwa JS, Huikari V, Cavadino A, Nolte IM, ... ... Oostra BA, et al. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Molecular Psychiatry. 20: 647-56. PMID 25288136 DOI: 10.1038/Mp.2014.107  0.56
2015 Broer L, Buchman AS, Deelen J, Evans DS, Faul JD, Lunetta KL, Sebastiani P, Smith JA, Smith AV, Tanaka T, Yu L, Arnold AM, Aspelund T, Benjamin EJ, De Jager PL, ... ... Oostra BA, et al. GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 70: 110-8. PMID 25199915 DOI: 10.1093/Gerona/Glu166  0.56
2014 Zhang Y, Bonnan A, Bony G, Ferezou I, Pietropaolo S, Ginger M, Sans N, Rossier J, Oostra B, LeMasson G, Frick A. Dendritic channelopathies contribute to neocortical and sensory hyperexcitability in Fmr1(-/y) mice. Nature Neuroscience. 17: 1701-9. PMID 25383903 DOI: 10.1038/Nn.3864  0.56
2014 van Leeuwen EM, Smouter FA, Kam-Thong T, Karbalai N, Smith AV, Harris TB, Launer LJ, Sitlani CM, Li G, Brody JA, Bis JC, White CC, Jaiswal A, Oostra BA, Hofman A, et al. The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels. Plos One. 9: e109290. PMID 25329471 DOI: 10.1371/Journal.Pone.0109290  0.4
2014 Springelkamp H, Höhn R, Mishra A, Hysi PG, Khor CC, Loomis SJ, Bailey JN, Gibson J, Thorleifsson G, Janssen SF, Luo X, Ramdas WD, Vithana E, Nongpiur ME, Montgomery GW, ... ... Oostra BA, et al. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nature Communications. 5: 4883. PMID 25241763 DOI: 10.1038/ncomms5883  0.56
2014 Simpson CL, Wojciechowski R, Oexle K, Murgia F, Portas L, Li X, Verhoeven VJ, Vitart V, Schache M, Hosseini SM, Hysi PG, Raffel LJ, Cotch MF, Chew E, Klein BE, ... ... Oostra BA, et al. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Plos One. 9: e107110. PMID 25233373 DOI: 10.1371/Journal.Pone.0107110  0.56
2014 Hysi PG, Cheng CY, Springelkamp H, Macgregor S, Bailey JN, Wojciechowski R, Vitart V, Nag A, Hewitt AW, Höhn R, Venturini C, Mirshahi A, Ramdas WD, Thorleifsson G, Vithana E, ... ... Oostra BA, et al. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics. 46: 1126-30. PMID 25173106 DOI: 10.1038/Ng.3087  0.56
2014 Broer L, Raschenberger J, Deelen J, Mangino M, Codd V, Pietiläinen KH, Albrecht E, Amin N, Beekman M, de Craen AJ, Gieger C, Haun M, Henneman P, Herder C, Hovatta I, ... ... Oostra BA, et al. Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants. European Journal of Epidemiology. 29: 629-38. PMID 25064619 DOI: 10.1007/s10654-014-9940-1  0.56
2014 Francioli LC, Menelaou A, Pulit SL, Van Dijk F, Palamara PF, Elbers CC, Neerincx PBT, Ye K, Guryev V, Kloosterman WP, Deelen P, Abdellaoui A, Van Leeuwen EM, Van Oven M, Vermaat M, ... ... Oostra B, et al. Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature Genetics. 46: 818-825. PMID 24974849 DOI: 10.1038/Ng.3021  0.56
2014 Albrecht E, Sillanpää E, Karrasch S, Alves AC, Codd V, Hovatta I, Buxton JL, Nelson CP, Broer L, Hägg S, Mangino M, Willemsen G, Surakka I, Ferreira MA, Amin N, ... Oostra BA, et al. Telomere length in circulating leukocytes is associated with lung function and disease. The European Respiratory Journal. 43: 983-92. PMID 24311771 DOI: 10.1183/09031936.00046213  0.56
2014 Liu F, Hendriks AE, Ralf A, Boot AM, Benyi E, Sävendahl L, Oostra BA, van Duijn C, Hofman A, Rivadeneira F, Uitterlinden AG, Drop SL, Kayser M. Common DNA variants predict tall stature in Europeans. Human Genetics. 133: 587-97. PMID 24253421 DOI: 10.1007/S00439-013-1394-0  0.56
2014 Iglesias AI, Springelkamp H, van der Linde H, Severijnen LA, Amin N, Oostra B, Kockx CE, van den Hout MC, van Ijcken WF, Hofman A, Uitterlinden AG, Verdijk RM, Klaver CC, Willemsen R, van Duijn CM. Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age. Human Molecular Genetics. 23: 1320-32. PMID 24150847 DOI: 10.1093/Hmg/Ddt522  0.36
2014 Boomsma DI, Wijmenga C, Slagboom EP, Swertz MA, Karssen LC, Abdellaoui A, Ye K, Guryev V, Vermaat M, Van Dijk F, Francioli LC, Hottenga JJ, Laros JFJ, Li Q, Li Y, ... ... Oostra B, et al. The Genome of the Netherlands: Design, and project goals European Journal of Human Genetics. 22: 221-227. PMID 23714750 DOI: 10.1038/Ejhg.2013.118  0.56
2014 Avery CL, Sitlani CM, Arking DE, Arnett DK, Bis JC, Boerwinkle E, Buckley BM, Ida Chen YD, de Craen AJ, Eijgelsheim M, Enquobahrie D, Evans DS, Ford I, Garcia ME, Gudnason V, ... ... Oostra BA, et al. Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. The Pharmacogenomics Journal. 14: 6-13. PMID 23459443 DOI: 10.1038/Tpj.2013.4  0.56
2013 Bagni C, Oostra BA. Fragile X syndrome: From protein function to therapy. American Journal of Medical Genetics. Part A. 161: 2809-21. PMID 24115651 DOI: 10.1002/Ajmg.A.36241  0.56
2013 Ansari M, McKeigue PM, Skerka C, Hayward C, Rudan I, Vitart V, Polasek O, Armbrecht AM, Yates JR, Vatavuk Z, Bencic G, Kolcic I, Oostra BA, Van Duijn CM, Campbell S, et al. Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration. Human Molecular Genetics. 22: 4857-69. PMID 23873044 DOI: 10.1093/Hmg/Ddt336  0.56
2013 Quadri M, Fang M, Picillo M, Olgiati S, Breedveld GJ, Graafland J, Wu B, Xu F, Erro R, Amboni M, Pappatà S, Quarantelli M, Annesi G, Quattrone A, Chien HF, ... ... Oostra BA, et al. Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. Human Mutation. 34: 1208-15. PMID 23804577 DOI: 10.1002/humu.22373  0.56
2013 Isaacs A, Willems SM, Bos D, Dehghan A, Hofman A, Ikram MA, Uitterlinden AG, Oostra BA, Franco OH, Witteman JC, van Duijn CM. Risk scores of common genetic variants for lipid levels influence atherosclerosis and incident coronary heart disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 33: 2233-9. PMID 23766260 DOI: 10.1161/Atvbaha.113.301236  0.56
2013 Randall JC, Winkler TW, Kutalik Z, Berndt SI, Jackson AU, Monda KL, Kilpeläinen TO, Esko T, Mägi R, Li S, Workalemahu T, Feitosa MF, Croteau-Chonka DC, Day FR, Fall T, ... ... Oostra BA, et al. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. Plos Genetics. 9: e1003500. PMID 23754948 DOI: 10.1371/Journal.Pgen.1003500  0.56
2013 Graff M, Ngwa JS, Workalemahu T, Homuth G, Schipf S, Teumer A, Völzke H, Wallaschofski H, Abecasis GR, Edward L, Francesco C, Sanna S, Scheet P, Schlessinger D, Sidore C, ... ... Oostra BA, et al. Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Human Molecular Genetics. 22: 3597-607. PMID 23669352 DOI: 10.1093/Hmg/Ddt205  0.56
2013 van der Loos MJ, Rietveld CA, Eklund N, Koellinger PD, Rivadeneira F, Abecasis GR, Ankra-Badu GA, Baumeister SE, Benjamin DJ, Biffar R, Blankenberg S, Boomsma DI, Cesarini D, Cucca F, de Geus EJ, ... ... Oostra BA, et al. The molecular genetic architecture of self-employment. Plos One. 8: e60542. PMID 23593239 DOI: 10.1371/Journal.Pone.0060542  0.56
2013 Fernández-Rhodes L, Demerath EW, Cousminer DL, Tao R, Dreyfus JG, Esko T, Smith AV, Gudnason V, Harris TB, Launer L, McArdle PF, Yerges-Armstrong LM, Elks CE, Strachan DP, Kutalik Z, ... ... Oostra B, et al. Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. American Journal of Epidemiology. 178: 451-60. PMID 23558354 DOI: 10.1093/Aje/Kws473  0.56
2013 Codd V, Nelson CP, Albrecht E, Mangino M, Deelen J, Buxton JL, Hottenga JJ, Fischer K, Esko T, Surakka I, Broer L, Nyholt DR, Mateo Leach I, Salo P, Hägg S, ... ... Oostra BA, et al. Identification of seven loci affecting mean telomere length and their association with disease. Nature Genetics. 45: 422-7, 427e1-2. PMID 23535734 DOI: 10.1038/Ng.2528  0.56
2013 Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, ... ... Oostra BA, et al. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Human Molecular Genetics. 22: 2754-64. PMID 23474815 DOI: 10.1093/Hmg/Ddt116  0.56
2013 Sun Y, Almomani R, Breedveld GJ, Santen GW, Aten E, Lefeber DJ, Hoff JI, Brusse E, Verheijen FW, Verdijk RM, Kriek M, Oostra B, Breuning MH, Losekoot M, den Dunnen JT, et al. Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease). Human Mutation. 34: 706-13. PMID 23418007 DOI: 10.1002/humu.22292  0.56
2013 Lopes MC, Hysi PG, Verhoeven VJ, Macgregor S, Hewitt AW, Montgomery GW, Cumberland P, Vingerling JR, Young TL, van Duijn CM, Oostra B, Uitterlinden AG, Rahi JS, Mackey DA, Klaver CC, et al. Identification of a candidate gene for astigmatism. Investigative Ophthalmology & Visual Science. 54: 1260-7. PMID 23322567 DOI: 10.1167/Iovs.12-10463  0.56
2013 Broer L, Codd V, Nyholt DR, Deelen J, Mangino M, Willemsen G, Albrecht E, Amin N, Beekman M, de Geus EJ, Henders A, Nelson CP, Steves CJ, Wright MJ, de Craen AJ, ... ... Oostra BA, et al. Meta-analysis of telomere length in 19,713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics : Ejhg. 21: 1163-8. PMID 23321625 DOI: 10.1038/Ejhg.2012.303  0.56
2013 Florisson JMG, Mathijssen IMJ, Dumee B, Hoogeboom JAM, Poddighe PJ, Oostra BA, Frijns JP, Koster L, de Klein A, Eussen B, de Vries BBA, Swagemakers S, van der Spek PJ, Verkerk AJMH. Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome American Journal of Medical Genetics, Part A. 161: 244-253. PMID 23303641 DOI: 10.1002/ajmg.a.35632  0.56
2013 Hek K, Demirkan A, Lahti J, Terracciano A, Teumer A, Cornelis MC, Amin N, Bakshis E, Baumert J, Ding J, Liu Y, Marciante K, Meirelles O, Nalls MA, Sun YV, ... ... Oostra BA, et al. A genome-wide association study of depressive symptoms. Biological Psychiatry. 73: 667-78. PMID 23290196 DOI: 10.1016/J.Biopsych.2012.09.033  0.56
2013 Amin N, Hottenga JJ, Hansell NK, Janssens AC, de Moor MH, Madden PA, Zorkoltseva IV, Penninx BW, Terracciano A, Uda M, Tanaka T, Esko T, Realo A, Ferrucci L, Luciano M, ... ... Oostra BA, et al. Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics : Ejhg. 21: 876-82. PMID 23211697 DOI: 10.1038/Ejhg.2012.263  0.56
2013 Demirkan A, Isaacs A, Ugocsai P, Liebisch G, Struchalin M, Rudan I, Wilson JF, Pramstaller PP, Gyllensten U, Campbell H, Schmitz G, Oostra BA, van Duijn CM. Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics study. Journal of Psychiatric Research. 47: 357-62. PMID 23207112 DOI: 10.1016/j.jpsychires.2012.11.001  0.56
2013 Stam AH, Weller CM, Janssens AC, Aulchenko YS, Oostra BA, Frants RR, van den Maagdenberg AM, Ferrari MD, van Duijn CM, Terwindt GM. Migraine is not associated with enhanced atherosclerosis. Cephalalgia : An International Journal of Headache. 33: 228-35. PMID 23147163 DOI: 10.1177/0333102412466966  0.4
2013 Gantois I, Pop AS, de Esch CE, Buijsen RA, Pooters T, Gomez-Mancilla B, Gasparini F, Oostra BA, D'Hooge R, Willemsen R. Chronic administration of AFQ056/Mavoglurant restores social behaviour in Fmr1 knockout mice. Behavioural Brain Research. 239: 72-9. PMID 23142366 DOI: 10.1016/j.bbr.2012.10.059  0.56
2013 Peters MJ, Broer L, Willemen HL, Eiriksdottir G, Hocking LJ, Holliday KL, Horan MA, Meulenbelt I, Neogi T, Popham M, Schmidt CO, Soni A, Valdes AM, Amin N, Dennison EM, ... ... Oostra B, et al. Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. Annals of the Rheumatic Diseases. 72: 427-36. PMID 22956598 DOI: 10.1136/Annrheumdis-2012-201742  0.56
2013 Van Den Berg L, Henneman P, Willems Van Dijk K, Delemarre-Van De Waal HA, Oostra BA, Van Duijn CM, Janssens ACJW. Heritability of dietary food intake patterns Acta Diabetologica. 50: 721-726. PMID 22415036 DOI: 10.1007/s00592-012-0387-0  0.56
2013 Randall JC, Winkler TW, Kutalik Z, Berndt SI, Jackson AU, Monda KL, Kilpeläinen TO, Esko T, Mägi R, Li S, Workalemahu T, Feitosa MF, Chonka DCC, Day FR, Fall T, ... ... Oostra BA, et al. Supplementary material 1 Tel Aviv: Journal of the Institute of Archaeology of Tel Aviv University. DOI: 10.1179/10.1179/1077352513Z.00000000072.S1  0.36
2013 Verhoeven VJM, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GHS, McMahon G, ... ... Oostra BA, et al. Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (Nature Genetics (2013) 45 (314-318)) Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712B  0.36
2012 Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, Chasman DI, Rose LM, Thorleifsson G, Steinthorsdottir V, Mägi R, Waite L, Smith AV, Yerges-Armstrong LM, Monda KL, Hadley D, ... ... Oostra BA, et al. FTO genotype is associated with phenotypic variability of body mass index. Nature. 490: 267-72. PMID 22982992 DOI: 10.1038/Nature11401  0.56
2012 Ibrahim-Verbaas CA, Zorkoltseva IV, Amin N, Schuur M, Coppus AM, Isaacs A, Aulchenko YS, Breteler MM, Ikram MA, Axenovich TI, Verbeek MM, van Swieten JC, Oostra BA, van Duijn CM. Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2. Human Genetics. 131: 1869-76. PMID 22872014 DOI: 10.1007/S00439-012-1210-2  0.4
2012 McQuillan R, Eklund N, Pirastu N, Kuningas M, McEvoy BP, Esko T, Corre T, Davies G, Kaakinen M, Lyytikäinen LP, Kristiansson K, Havulinna AS, Gögele M, Vitart V, Tenesa A, ... ... Oostra B, et al. Evidence of inbreeding depression on human height. Plos Genetics. 8: e1002655. PMID 22829771 DOI: 10.1371/Journal.Pgen.1002655  0.56
2012 Durik M, Kavousi M, van der Pluijm I, Isaacs A, Cheng C, Verdonk K, Loot AE, Oeseburg H, Bhaggoe UM, Leijten F, van Veghel R, de Vries R, Rudez G, Brandt R, Ridwan YR, ... ... Oostra BA, et al. Nucleotide excision DNA repair is associated with age-related vascular dysfunction. Circulation. 126: 468-78. PMID 22705887 DOI: 10.1161/Circulationaha.112.104380  0.56
2012 Perry JR, Voight BF, Yengo L, Amin N, Dupuis J, Ganser M, Grallert H, Navarro P, Li M, Qi L, Steinthorsdottir V, Scott RA, Almgren P, Arking DE, Aulchenko Y, ... ... Oostra B, et al. Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. Plos Genetics. 8: e1002741. PMID 22693455 DOI: 10.1371/Journal.Pgen.1002741  0.56
2012 Liu CT, Estrada K, Yerges-Armstrong LM, Amin N, Evangelou E, Li G, Minster RL, Carless MA, Kammerer CM, Oei L, Zhou Y, Alonso N, Dailiana Z, Eriksson J, García-Giralt N, ... ... Oostra BA, et al. Assessment of gene-by-sex interaction effect on bone mineral density. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 27: 2051-64. PMID 22692763 DOI: 10.1002/Jbmr.1679  0.56
2012 Verhoeven VJ, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, Cotch MF, Yamashiro K, Baird PN, Mackey DA, Wojciechowski R, Ikram MK, Hewitt AW, Duggal P, Janmahasatian S, ... ... Oostra BA, et al. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Human Genetics. 131: 1467-80. PMID 22665138 DOI: 10.1007/S00439-012-1176-0  0.56
2012 Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, RaÅ¡in MR, Sousa AM, Fertuzinhos S, Chen JG, Arellano JI, Chan DW, Pletikos M, Vasung L, Rowitch DH, Huang EJ, ... ... Oostra BA, et al. Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex. Cell. 149: 899-911. PMID 22579290 DOI: 10.1016/J.Cell.2012.02.060  0.56
2012 van Koolwijk LM, Ramdas WD, Ikram MK, Jansonius NM, Pasutto F, Hysi PG, Macgregor S, Janssen SF, Hewitt AW, Viswanathan AC, ten Brink JB, Hosseini SM, Amin N, Despriet DD, Willemse-Assink JJ, ... ... Oostra BA, et al. Common genetic determinants of intraocular pressure and primary open-angle glaucoma. Plos Genetics. 8: e1002611. PMID 22570627 DOI: 10.1371/Journal.Pgen.1002611  0.56
2012 French VM, van de Laar IM, Wessels MW, Rohe C, Roos-Hesselink JW, Wang G, Frohn-Mulder IM, Severijnen LA, de Graaf BM, Schot R, Breedveld G, Mientjes E, van Tienhoven M, Jadot E, Jiang Z, ... ... Oostra BA, et al. NPHP4 variants are associated with pleiotropic heart malformations. Circulation Research. 110: 1564-74. PMID 22550138 DOI: 10.1161/CIRCRESAHA.112.269795  0.56
2012 Bis JC, DeCarli C, Smith AV, van der Lijn F, Crivello F, Fornage M, Debette S, Shulman JM, Schmidt H, Srikanth V, Schuur M, Yu L, Choi SH, Sigurdsson S, Verhaaren BF, ... ... Oostra BA, et al. Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics. 44: 545-51. PMID 22504421 DOI: 10.1038/Ng.2237  0.56
2012 Ameur A, Enroth S, Johansson A, Zaboli G, Igl W, Johansson AC, Rivas MA, Daly MJ, Schmitz G, Hicks AA, Meitinger T, Feuk L, van Duijn C, Oostra B, Pramstaller PP, et al. Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids. American Journal of Human Genetics. 90: 809-20. PMID 22503634 DOI: 10.1016/J.Ajhg.2012.03.014  0.56
2012 Demirkan A, van Duijn CM, Ugocsai P, Isaacs A, Pramstaller PP, Liebisch G, Wilson JF, Johansson Ã…, Rudan I, Aulchenko YS, Kirichenko AV, Janssens AC, Jansen RC, Gnewuch C, Domingues FS, ... ... Oostra BA, et al. Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. Plos Genetics. 8: e1002490. PMID 22359512 DOI: 10.1371/Journal.Pgen.1002490  0.56
2012 Gasten AC, Ramdas WD, Broer L, van Koolwijk LME, Kamran Ikram M, de Jong PTVM, Aulchenko YS, Wolfs RC, Hofman A, Rivadeneira F, Uitterlinden AG, Oostra BA, Lemij HG, Klaver CCW, Jansonius NM, et al. A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology Investigative Ophthalmology and Visual Science. 53: 1485-1491. PMID 22266513 DOI: 10.1167/Iovs.11-7384  0.56
2012 Luciano M, Lopez LM, de Moor MH, Harris SE, Davies G, Nutile T, Krueger RF, Esko T, Schlessinger D, Toshiko T, Derringer JL, Realo A, Hansell NK, Pergadia ML, Pesonen AK, ... ... Oostra BA, et al. Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 192-200. PMID 22213687 DOI: 10.1002/Ajmg.B.32013  0.56
2012 Mitchell GF, Verwoert GC, Tarasov KV, Isaacs A, Smith AV, Yasmin, Rietzschel ER, Tanaka T, Liu Y, Parsa A, Najjar SS, O'Shaughnessy KM, Sigurdsson S, De Buyzere ML, Larson MG, ... ... Oostra BA, et al. Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium. Circulation. Cardiovascular Genetics. 5: 81-90. PMID 22068335 DOI: 10.1161/Circgenetics.111.959817  0.56
2012 Zaboli G, Ameur A, Igl W, Johansson Ã…, Hayward C, Vitart V, Campbell S, Zgaga L, Polasek O, Schmitz G, van Duijn C, Oostra B, Pramstaller P, Hicks A, Meitinger T, et al. Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits. European Journal of Human Genetics : Ejhg. 20: 77-83. PMID 21811304 DOI: 10.1038/ejhg.2011.138  0.56
2011 Punzo F, Bertoli-Avella AM, Scianguetta S, Della Ragione F, Casale M, Ronzoni L, Cappellini MD, Forni G, Oostra BA, Perrotta S. Congenital dyserythropoietic anemia type II: Molecular analysis and expression of the SEC23B Gene Orphanet Journal of Rare Diseases. 6. PMID 22208203 DOI: 10.1186/1750-1172-6-89  0.56
2011 Broer L, Koudstaal PJ, Amin N, Rivadeneira F, Uitterlinden AG, Hofman A, Oostra BA, Breteler MM, Ikram MA, van Duijn CM. Association of heat shock proteins with Parkinson's disease. European Journal of Epidemiology. 26: 933-5. PMID 22120601 DOI: 10.1007/S10654-011-9635-9  0.56
2011 Axenovich T, Zorkoltseva I, Belonogova N, van Koolwijk LM, van Koolwijk L, Borodin P, Kirichenko A, Babenko V, Ramdas WD, Ramdas W, Amin N, Despriet DD, Despriet D, Vingerling JR, Vingerling J, ... ... Oostra BA, et al. Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population. Journal of Medical Genetics. 48: 802-9. PMID 22058429 DOI: 10.1136/jmedgenet-2011-100436  0.56
2011 Bis JC, Kavousi M, Franceschini N, Isaacs A, Abecasis GR, Schminke U, Post WS, Smith AV, Cupples LA, Markus HS, Schmidt R, Huffman JE, Lehtimäki T, Baumert J, Münzel T, ... ... Oostra B, et al. Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nature Genetics. 43: 940-7. PMID 21909108 DOI: 10.1038/Ng.920  0.56
2011 Ramdas WD, van Koolwijk LM, Cree AJ, Janssens AC, Amin N, de Jong PT, Wolfs RC, Gibson J, Kirwan JF, Hofman A, Rivadeneira F, Oostra BA, Uitterlinden AG, Ennis S, Lotery AJ, et al. Clinical implications of old and new genes for open-angle glaucoma. Ophthalmology. 118: 2389-97. PMID 21872936 DOI: 10.1016/J.Ophtha.2011.05.040  0.36
2011 Nalls MA, Couper DJ, Tanaka T, van Rooij FJ, Chen MH, Smith AV, Toniolo D, Zakai NA, Yang Q, Greinacher A, Wood AR, Garcia M, Gasparini P, Liu Y, Lumley T, ... ... Oostra BA, et al. Multiple loci are associated with white blood cell phenotypes. Plos Genetics. 7: e1002113. PMID 21738480 DOI: 10.1371/Journal.Pgen.1002113  0.56
2011 Kilpeläinen TO, Zillikens MC, Stančákova A, Finucane FM, Ried JS, Langenberg C, Zhang W, Beckmann JS, Luan J, Vandenput L, Styrkarsdottir U, Zhou Y, Smith AV, Zhao JH, Amin N, ... ... Oostra BA, et al. Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Nature Genetics. 43: 753-60. PMID 21706003 DOI: 10.1038/Ng.866  0.56
2011 Guo W, Allan AM, Zong R, Zhang L, Johnson EB, Schaller EG, Murthy AC, Goggin SL, Eisch AJ, Oostra BA, Nelson DL, Jin P, Zhao X. Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning. Nature Medicine. 17: 559-65. PMID 21516088 DOI: 10.1038/Nm.2336  0.56
2011 Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D, Desrivières S, Aliev FA, Khan AA, Amin N, Aulchenko YS, Bakalkin G, Bakker SJ, Balkau B, Beulens JW, ... ... Oostra BA, et al. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America. 108: 7119-24. PMID 21471458 DOI: 10.1073/Pnas.1017288108  0.56
2011 Ligthart L, de Vries B, Smith AV, Ikram MA, Amin N, Hottenga JJ, Koelewijn SC, Kattenberg VM, de Moor MH, Janssens AC, Aulchenko YS, Oostra BA, de Geus EJ, Smit JH, Zitman FG, et al. Meta-analysis of genome-wide association for migraine in six population-based European cohorts. European Journal of Human Genetics : Ejhg. 19: 901-7. PMID 21448238 DOI: 10.1038/Ejhg.2011.48  0.56
2011 Demirkan A, Amin N, Isaacs A, Jarvelin MR, Whitfield JB, Wichmann HE, Kyvik KO, Rudan I, Gieger C, Hicks AA, Johansson Å, Hottenga JJ, Smith JJ, Wild SH, Pedersen NL, ... ... Oostra BA, et al. Genetic architecture of circulating lipid levels. European Journal of Human Genetics : Ejhg. 19: 813-9. PMID 21448234 DOI: 10.1038/Ejhg.2011.21  0.56
2011 Ramdas WD, van Koolwijk LM, Lemij HG, Pasutto F, Cree AJ, Thorleifsson G, Janssen SF, Jacoline TB, Amin N, Rivadeneira F, Wolfs RC, Walters GB, Jonasson F, Weisschuh N, Mardin CY, ... ... Oostra BA, et al. Common genetic variants associated with open-angle glaucoma. Human Molecular Genetics. 20: 2464-71. PMID 21427129 DOI: 10.1093/Hmg/Ddr120  0.56
2011 Broer L, Ikram MA, Schuur M, DeStefano AL, Bis JC, Liu F, Rivadeneira F, Uitterlinden AG, Beiser AS, Longstreth WT, Hofman A, Aulchenko Y, Seshadri S, Fitzpatrick AL, Oostra BA, et al. Association of HSP70 and its co-chaperones with Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 25: 93-102. PMID 21403392 DOI: 10.3233/Jad-2011-101560  0.56
2011 Levenga J, Hayashi S, de Vrij FM, Koekkoek SK, van der Linde HC, Nieuwenhuizen I, Song C, Buijsen RA, Pop AS, Gomezmancilla B, Nelson DL, Willemsen R, Gasparini F, Oostra BA. AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome. Neurobiology of Disease. 42: 311-7. PMID 21316452 DOI: 10.1016/j.nbd.2011.01.022  0.56
2011 Scotto-Lomassese S, Nissant A, Mota T, Néant-Féry M, Oostra BA, Greer CA, Lledo PM, Trembleau A, Caillé I. Fragile X mental retardation protein regulates new neuron differentiation in the adult olfactory bulb. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 2205-15. PMID 21307257 DOI: 10.1523/Jneurosci.5514-10.2011  0.56
2011 van de Laar IM, Oldenburg RA, Pals G, Roos-Hesselink JW, de Graaf BM, Verhagen JM, Hoedemaekers YM, Willemsen R, Severijnen LA, Venselaar H, Vriend G, Pattynama PM, Collée M, Majoor-Krakauer D, Poldermans D, ... ... Oostra BA, et al. Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis. Nature Genetics. 43: 121-6. PMID 21217753 DOI: 10.1038/Ng.744  0.56
2011 Ramdas WD, Amin N, van Koolwijk LM, Janssens AC, Demirkan A, de Jong PT, Aulchenko YS, Wolfs RC, Hofman A, Rivadeneira F, Uitterlinden AG, Oostra BA, Lemij HG, Klaver CC, Vingerling JR, et al. Genetic architecture of open angle glaucoma and related determinants. Journal of Medical Genetics. 48: 190-6. PMID 21059592 DOI: 10.1136/Jmg.2010.083337  0.4
2011 Santoro L, Breedveld GJ, Manganelli F, Iodice R, Pisciotta C, Nolano M, Punzo F, Quarantelli M, Pappatà S, Di Fonzo A, Oostra BA, Bonifati V. Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. Neurogenetics. 12: 33-9. PMID 20853184 DOI: 10.1007/s10048-010-0259-0  0.56
2011 Schuur M, van Swieten JC, Schol-Gelok S, Ikram MA, Vernooij MW, Liu F, Isaacs A, de Boer R, de Koning I, Niessen WJ, Vrooman H, Oostra BA, van der Lugt A, Breteler MM, van Duijn CM. Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 41-4. PMID 20667857 DOI: 10.1136/Jnnp.2009.176362  0.4
2011 Schuur M, Ikram MA, van Swieten JC, Isaacs A, Vergeer-Drop JM, Hofman A, Oostra BA, Breteler MM, van Duijn CM. Cathepsin D gene and the risk of Alzheimer's disease: a population-based study and meta-analysis. Neurobiology of Aging. 32: 1607-14. PMID 19926167 DOI: 10.1016/J.Neurobiolaging.2009.10.011  0.4
2011 Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D, Desrivières S, Aliev FA, Khan AA, Amin N, Aulchenko YS, Bakalkin G, Bakker SJ, Balkau B, Beulens JW, ... ... Oostra BA, et al. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) Proceedings of the National Academy of Sciences of the United States of America. 108: 9316. DOI: 10.1073/Pnas.1106917108  0.56
2010 Sotoodehnia N, Isaacs A, de Bakker PI, Dörr M, Newton-Cheh C, Nolte IM, van der Harst P, Müller M, Eijgelsheim M, Alonso A, Hicks AA, Padmanabhan S, Hayward C, Smith AV, Polasek O, ... ... Oostra BA, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nature Genetics. 42: 1068-76. PMID 21076409 DOI: 10.1038/Ng.716  0.56
2010 Solouki AM, Verhoeven VJ, van Duijn CM, Verkerk AJ, Ikram MK, Hysi PG, Despriet DD, van Koolwijk LM, Ho L, Ramdas WD, Czudowska M, Kuijpers RW, Amin N, Struchalin M, Aulchenko YS, ... ... Oostra BA, et al. A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. Nature Genetics. 42: 897-901. PMID 20835239 DOI: 10.1038/Ng.663  0.56
2010 Eijgelsheim M, Newton-Cheh C, Sotoodehnia N, de Bakker PI, Müller M, Morrison AC, Smith AV, Isaacs A, Sanna S, Dörr M, Navarro P, Fuchsberger C, Nolte IM, de Geus EJ, Estrada K, ... ... Oostra BA, et al. Genome-wide association analysis identifies multiple loci related to resting heart rate. Human Molecular Genetics. 19: 3885-94. PMID 20639392 DOI: 10.1093/Hmg/Ddq303  0.56
2010 Ramdas WD, van Koolwijk LM, Ikram MK, Jansonius NM, de Jong PT, Bergen AA, Isaacs A, Amin N, Aulchenko YS, Wolfs RC, Hofman A, Rivadeneira F, Oostra BA, Uitterlinden AG, Hysi P, et al. A genome-wide association study of optic disc parameters. Plos Genetics. 6: e1000978. PMID 20548946 DOI: 10.1371/Journal.Pgen.1000978  0.4
2010 Schol-Gelok S, Janssens ACJW, Tiemeier H, Liu F, Lopez-Leon S, Zorkoltseva IV, Axenovich TI, Swieten JCv, Uitterlinden AG, Hofman A, Aulchenko YS, Oostra BA, Duijn CMv. A Genome-Wide Screen for Depression in Two Independent Dutch Populations Biological Psychiatry. 68: 187-196. PMID 20452571 DOI: 10.1016/J.Biopsych.2010.01.033  0.36
2010 Breedveld GJ, Fabbrini G, Oostra BA, Berardelli A, Bonifati V. Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred. Neurogenetics. 11: 417-23. PMID 20437249 DOI: 10.1007/S10048-010-0244-7  0.56
2010 Köttgen A, Pattaro C, Böger CA, Fuchsberger C, Olden M, Glazer NL, Parsa A, Gao X, Yang Q, Smith AV, O'Connell JR, Li M, Schmidt H, Tanaka T, Isaacs A, ... ... Oostra BA, et al. New loci associated with kidney function and chronic kidney disease. Nature Genetics. 42: 376-84. PMID 20383146 DOI: 10.1038/Ng.568  0.56
2010 Pattaro C, De Grandi A, Vitart V, Hayward C, Franke A, Aulchenko YS, Johansson A, Wild SH, Melville SA, Isaacs A, Polasek O, Ellinghaus D, Kolcic I, Nöthlings U, Zgaga L, ... ... Oostra BA, et al. A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. Bmc Medical Genetics. 11: 41. PMID 20222955 DOI: 10.1186/1471-2350-11-41  0.56
2010 Collins SC, Coffee B, Benke PJ, Berry-Kravis E, Gilbert F, Oostra B, Halley D, Zwick ME, Cutler DJ, Warren ST. Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. Plos One. 5: e9476. PMID 20221430 DOI: 10.1371/Journal.Pone.0009476  0.56
2010 Henneman P, Aulchenko YS, Frants RR, Zorkoltseva IV, Zillikens MC, Frolich M, Oostra BA, van Dijk KW, van Duijn CM. Genetic architecture of plasma adiponectin overlaps with the genetics of metabolic syndrome-related traits. Diabetes Care. 33: 908-13. PMID 20067957 DOI: 10.2337/Dc09-1385  0.4
2010 Igl W, Johansson A, Wilson JF, Wild SH, Polasek O, Hayward C, Vitart V, Hastie N, Rudan P, Gnewuch C, Schmitz G, Meitinger T, Pramstaller PP, Hicks AA, Oostra BA, et al. Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. Plos Genetics. 6: e1000798. PMID 20066028 DOI: 10.1371/journal.pgen.1000798  0.56
2010 Heid IM, Henneman P, Hicks A, Coassin S, Winkler T, Aulchenko YS, Fuchsberger C, Song K, Hivert MF, Waterworth DM, Timpson NJ, Richards JB, Perry JR, Tanaka T, Amin N, ... ... Oostra BA, et al. Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. Atherosclerosis. 208: 412-20. PMID 20018283 DOI: 10.1016/J.Atherosclerosis.2009.11.035  0.56
2010 Zillikens MC, Uitterlinden AG, van Leeuwen JP, Berends AL, Henneman P, van Dijk KW, Oostra BA, van Duijn CM, Pols HA, Rivadeneira F. The role of body mass index, insulin, and adiponectin in the relation between fat distribution and bone mineral density. Calcified Tissue International. 86: 116-25. PMID 19957167 DOI: 10.1007/s00223-009-9319-6  0.4
2010 Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Floyd J, Hastie N, Knott S, Lauc G, ... ... Oostra BA, et al. Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. Obesity (Silver Spring, Md.). 18: 803-8. PMID 19851299 DOI: 10.1038/oby.2009.359  0.56
2010 Vegt R, Bertoli-Avella AM, Tulen JHM, De Graaf B, Verkerk AJMH, Vervoort J, Twigt CM, Maat-Kievit A, Van Tuijl R, Van Der Lijn M, Hengeveld MW, Oostra BA. Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorder European Journal of Human Genetics. 18: 206-211. PMID 19707245 DOI: 10.1038/ejhg.2009.148  0.56
2010 Liu F, Pardo LM, Schuur M, Sanchez-Juan P, Isaacs A, Sleegers K, de Koning I, Zorkoltseva IV, Axenovich TI, Witteman JC, Janssens AC, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM. The apolipoprotein E gene and its age-specific effects on cognitive function. Neurobiology of Aging. 31: 1831-3. PMID 19004527 DOI: 10.1016/j.neurobiolaging.2008.09.015  0.4
2010 Schuur M, Hommel D, Ikram MA, Amin N, Zorkoltseva IV, Kirichenko A, Koning Id, Janssens ACJW, Axenovich TI, Aulchenko YS, Hofman A, Breteler MMB, Oostra BA, Swieten JCv, Duijn CMv. Genome-wide linkage screen of cognitive function identifies susceptible chromosomal regions Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.346  0.56
2010 Willemsen R, Li Y, Berman RF, Brouwer JR, Oostra BA, Jin P. Animal models for FXTAS The Fragile X-Associated Tremor Ataxia Syndrome (Fxtas). 123-136. DOI: 10.1007/978-1-4419-5805-1_8  0.56
2009 Marroni F, Pfeufer A, Aulchenko YS, Franklin CS, Isaacs A, Pichler I, Wild SH, Oostra BA, Wright AF, Campbell H, Witteman JC, Kääb S, Hicks AA, Gyllensten U, Rudan I, et al. A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. Circulation. Cardiovascular Genetics. 2: 322-8. PMID 20031603 DOI: 10.1161/Circgenetics.108.833806  0.56
2009 den Broeder MJ, van der Linde H, Brouwer JR, Oostra BA, Willemsen R, Ketting RF. Generation and characterization of FMR1 knockout zebrafish. Plos One. 4: e7910. PMID 19936290 DOI: 10.1371/Journal.Pone.0007910  0.56
2009 Ganesh SK, Zakai NA, van Rooij FJ, Soranzo N, Smith AV, Nalls MA, Chen MH, Kottgen A, Glazer NL, Dehghan A, Kuhnel B, Aspelund T, Yang Q, Tanaka T, Jaffe A, ... ... Oostra BA, et al. Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nature Genetics. 41: 1191-8. PMID 19862010 DOI: 10.1038/Ng.466  0.56
2009 Richards JB, Kavvoura FK, Rivadeneira F, Styrkársdóttir U, Estrada K, Halldórsson BV, Hsu YH, Zillikens MC, Wilson SG, Mullin BH, Amin N, Aulchenko YS, Cupples LA, Deloukas P, Demissie S, ... ... Oostra BA, et al. Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture. Annals of Internal Medicine. 151: 528-37. PMID 19841454 DOI: 10.7326/0003-4819-151-8-200910200-00006  0.56
2009 Hoppenbrouwers IA, Aulchenko YS, Janssens AC, Ramagopalan SV, Broer L, Kayser M, Ebers GC, Oostra BA, Van Duijn CM, Hintzen RQ. Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis Journal of Human Genetics. 54: 676-680. PMID 19834503 DOI: 10.1038/jhg.2009.96  0.56
2009 Rivadeneira F, Styrkársdottir U, Estrada K, Halldórsson BV, Hsu YH, Richards JB, Zillikens MC, Kavvoura FK, Amin N, Aulchenko YS, Cupples LA, Deloukas P, Demissie S, Grundberg E, Hofman A, ... ... Oostra B, et al. Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. Nature Genetics. 41: 1199-206. PMID 19801982 DOI: 10.1038/Ng.446  0.56
2009 Hicks AA, Pramstaller PP, Johansson A, Vitart V, Rudan I, Ugocsai P, Aulchenko Y, Franklin CS, Liebisch G, Erdmann J, Jonasson I, Zorkoltseva IV, Pattaro C, Hayward C, Isaacs A, ... ... Oostra BA, et al. Genetic determinants of circulating sphingolipid concentrations in European populations. Plos Genetics. 5: e1000672. PMID 19798445 DOI: 10.1371/journal.pgen.1000672  0.56
2009 Zillikens MC, van Meurs JB, Rivadeneira F, Amin N, Hofman A, Oostra BA, Sijbrands EJ, Witteman JC, Pols HA, van Duijn CM, Uitterlinden AG. SIRT1 genetic variation is related to BMI and risk of obesity. Diabetes. 58: 2828-34. PMID 19741164 DOI: 10.2337/Db09-0536  0.4
2009 Liu F, Ikram MA, Janssens AC, Schuur M, de Koning I, Isaacs A, Struchalin M, Uitterlinden AG, den Dunnen JT, Sleegers K, Bettens K, Van Broeckhoven C, van Swieten J, Hofman A, Oostra BA, et al. A study of the SORL1 gene in Alzheimer's disease and cognitive function. Journal of Alzheimer's Disease : Jad. 18: 51-64. PMID 19584446 DOI: 10.3233/Jad-2009-1137  0.4
2009 Estrada K, Krawczak M, Schreiber S, van Duijn K, Stolk L, van Meurs JB, Liu F, Penninx BW, Smit JH, Vogelzangs N, Hottenga JJ, Willemsen G, de Geus EJ, Lorentzon M, von Eller-Eberstein H, ... ... Oostra BA, et al. A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. Human Molecular Genetics. 18: 3516-24. PMID 19570815 DOI: 10.1093/Hmg/Ddp296  0.56
2009 Heard-Costa NL, Zillikens MC, Monda KL, Johansson A, Harris TB, Fu M, Haritunians T, Feitosa MF, Aspelund T, Eiriksdottir G, Garcia M, Launer LJ, Smith AV, Mitchell BD, McArdle PF, ... ... Oostra BA, et al. NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. Plos Genetics. 5: e1000539. PMID 19557197 DOI: 10.1371/Journal.Pgen.1000539  0.56
2009 Lindgren CM, Heid IM, Randall JC, Lamina C, Steinthorsdottir V, Qi L, Speliotes EK, Thorleifsson G, Willer CJ, Herrera BM, Jackson AU, Lim N, Scheet P, Soranzo N, Amin N, ... ... Oostra BA, et al. Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. Plos Genetics. 5: e1000508. PMID 19557161 DOI: 10.1371/Journal.Pgen.1000508  0.56
2009 Di Fonzo A, Fabrizio E, Thomas A, Fincati E, Marconi R, Tinazzi M, Breedveld GJ, Simons EJ, Chien HF, Ferreira JJ, Horstink MW, Abbruzzese G, Borroni B, Cossu G, Dalla Libera A, ... ... Oostra BA, et al. GIGYF2 mutations are not a frequent cause of familial Parkinson's disease. Parkinsonism & Related Disorders. 15: 703-5. PMID 19482505 DOI: 10.1016/j.parkreldis.2009.05.001  0.56
2009 Axenovich TI, Zorkoltseva IV, Belonogova NM, Struchalin MV, Kirichenko AV, Kayser M, Oostra BA, van Duijn CM, Aulchenko YS. Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population. Human Genetics. 126: 457-71. PMID 19466457 DOI: 10.1007/s00439-009-0686-x  0.56
2009 Levenga J, Buijsen RA, Rifé M, Moine H, Nelson DL, Oostra BA, Willemsen R, de Vrij FM. Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons. Neurobiology of Disease. 35: 241-50. PMID 19464371 DOI: 10.1016/j.nbd.2009.05.004  0.56
2009 Pattaro C, Aulchenko YS, Isaacs A, Vitart V, Hayward C, Franklin CS, Polasek O, Kolcic I, Biloglav Z, Campbell S, Hastie N, Lauc G, Meitinger T, Oostra BA, Gyllensten U, et al. Genome-wide linkage analysis of serum creatinine in three isolated European populations. Kidney International. 76: 297-306. PMID 19387472 DOI: 10.1038/ki.2009.135  0.56
2009 Hashem V, Galloway JN, Mori M, Willemsen R, Oostra BA, Paylor R, Nelson DL. Ectopic expression of CGG containing mRNA is neurotoxic in mammals. Human Molecular Genetics. 18: 2443-51. PMID 19377084 DOI: 10.1093/hmg/ddp182  0.56
2009 Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, Debette S, Lumley T, Folsom AR, van den Herik EG, Bos MJ, Beiser A, Cushman M, Launer LJ, Shahar E, ... ... Oostra BA, et al. Genomewide association studies of stroke. The New England Journal of Medicine. 360: 1718-28. PMID 19369658 DOI: 10.1056/Nejmoa0900094  0.56
2009 Aulchenko YS, Struchalin MV, Belonogova NM, Axenovich TI, Weedon MN, Hofman A, Uitterlinden AG, Kayser M, Oostra BA, Duijn CMv, Janssens ACJW, Borodin PM. Predicting human height by Victorian and genomic methods. European Journal of Human Genetics. 17: 1070-1075. PMID 19223933 DOI: 10.1038/Ejhg.2009.5  0.36
2009 Savoia A, Noris P, Perrotta S, Punzo F, Rocco DD, Oostra BA, Balduini CL. Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin Platelets. 20: 72-73. PMID 19172527 DOI: 10.1080/09537100802485129  0.56
2009 Despriet DDG, van Duijn CM, Oostra BA, Uitterlinden AG, Hofman A, Wright AF, ten Brink JB, Bakker A, de Jong PTVM, Vingerling JR, Bergen AAB, Klaver CCW. Complement Component C3 and Risk of Age-Related Macular Degeneration Ophthalmology. 116: 474-480.e2. PMID 19168221 DOI: 10.1016/J.Ophtha.2008.09.055  0.56
2009 Amin N, Aulchenko YS, Dekker MC, Ferdinand RF, van Spreeken A, Temmink AH, Verhulst FC, Oostra BA, van Duijn CM. Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population. European Journal of Human Genetics : Ejhg. 17: 958-66. PMID 19156173 DOI: 10.1038/Ejhg.2008.260  0.4
2009 Ikram MA, Liu F, Oostra BA, Hofman A, van Duijn CM, Breteler MM. The GAB2 gene and the risk of Alzheimer's disease: replication and meta-analysis. Biological Psychiatry. 65: 995-9. PMID 19118819 DOI: 10.1016/J.Biopsych.2008.11.014  0.36
2009 Pilpel Y, Kolleker A, Berberich S, Ginger M, Frick A, Mientjes E, Oostra BA, Seeburg PH. Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice. The Journal of Physiology. 587: 787-804. PMID 19103683 DOI: 10.1113/Jphysiol.2008.160929  0.56
2009 Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, ... ... Oostra BA, et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics. 41: 47-55. PMID 19060911 DOI: 10.1038/Ng.269  0.56
2009 Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Dunlop MG, Floyd J, Hastie N, Hofman A, ... ... Oostra BA, et al. Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Human Molecular Genetics. 18: 373-80. PMID 18952825 DOI: 10.1093/Hmg/Ddn350  0.56
2009 Rivadeneira F, Styrkarsdottir U, Estrada K, Halldorsson B, Hsu Y, Richards JB, Zillikens MC, Kavvoura F, Amin N, Aulchenko Y, Cupples L, Deloukas P, Demissie S, Grundberg E, Hofman A, ... ... Oostra B, et al. Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets Bone. 44. DOI: 10.1016/J.Bone.2009.03.085  0.56
2008 Coppus AM, Evenhuis HM, Verberne GJ, Visser FE, Oostra BA, Eikelenboom P, van Gool WA, Janssens AC, van Duijn CM. Survival in elderly persons with Down syndrome. Journal of the American Geriatrics Society. 56: 2311-6. PMID 19093931 DOI: 10.1111/j.1532-5415.2008.01999.x  0.56
2008 Brouwer JR, Huizer K, Severijnen LA, Hukema RK, Berman RF, Oostra BA, Willemsen R. CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome. Journal of Neurochemistry. 107: 1671-82. PMID 19014369 DOI: 10.1111/J.1471-4159.2008.05747.X  0.56
2008 Aulchenko YS, Hoppenbrouwers IA, Ramagopalan SV, Broer L, Jafari N, Hillert J, Link J, Lundström W, Greiner E, Dessa Sadovnick A, Goossens D, Van Broeckhoven C, Del-Favero J, Ebers GC, Oostra BA, et al. Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. Nature Genetics. 40: 1402-3. PMID 18997785 DOI: 10.1038/Ng.251  0.56
2008 Dehghan A, van Hoek M, Sijbrands EJ, Oostra BA, Hofman A, van Duijn CM, Witteman JC. Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study. Bmc Medicine. 6: 30. PMID 18925945 DOI: 10.1186/1741-7015-6-30  0.4
2008 van Hoek M, Dehghan A, Witteman JC, van Duijn CM, Uitterlinden AG, Oostra BA, Hofman A, Sijbrands EJ, Janssens AC. Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study. Diabetes. 57: 3122-8. PMID 18694974 DOI: 10.2337/Db08-0425  0.4
2008 Zhang J, Fang Z, Jud C, Vansteensel MJ, Kaasik K, Lee CC, Albrecht U, Tamanini F, Meijer JH, Oostra BA, Nelson DL. Fragile X-related proteins regulate mammalian circadian behavioral rhythms. American Journal of Human Genetics. 83: 43-52. PMID 18589395 DOI: 10.1016/j.ajhg.2008.06.003  0.56
2008 de Vrij FM, Levenga J, van der Linde HC, Koekkoek SK, De Zeeuw CI, Nelson DL, Oostra BA, Willemsen R. Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice. Neurobiology of Disease. 31: 127-32. PMID 18571098 DOI: 10.1016/j.nbd.2008.04.002  0.56
2008 Janssens ACJW, Gwinn M, Bradley LA, Oostra BA, van Duijn CM, Khoury MJ. A Critical Appraisal of the Scientific Basis of Commercial Genomic Profiles Used to Assess Health Risks and Personalize Health Interventions American Journal of Human Genetics. 82: 593-599. PMID 18319070 DOI: 10.1016/j.ajhg.2007.12.020  0.56
2007 Aulchenko YS, Pullen J, Kloosterman WP, Yazdanpanah M, Hofman A, Vaessen N, Snijders PJ, Zubakov D, Mackay I, Olavesen M, Sidhu B, Smith VE, Carey A, Berezikov E, Uitterlinden AG, ... ... Oostra BA, et al. LPIN2 is associated with type 2 diabetes, glucose metabolism, and body composition. Diabetes. 56: 3020-6. PMID 17804763 DOI: 10.2337/Db07-0338  0.56
2007 Fabbrini G, Pasquini M, Aurilia C, Berardelli I, Breedveld G, Oostra BA, Bonifati V, Berardelli A. A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 2229-34. PMID 17712845 DOI: 10.1002/Mds.21697  0.56
2007 Arias-Vásquez A, Lau Ld, Pardo L, Liu F, Feng B, Bertoli-Avella A, Isaacs A, Aulchenko Y, Hofman A, Oostra B, Breteler M, Duijn Cv. Relationship of the Ubiquilin 1 gene with Alzheimer's and Parkinson's disease and cognitive function. Neuroscience Letters. 424: 1-5. PMID 17709205 DOI: 10.1016/J.Neulet.2007.07.015  0.36
2007 Isaacs A, Sayed-Tabatabaei FA, Hofman A, Oostra BA, Klungel OH, Zee AM, Stricker BHC, Witteman JCM, Duijn CMv. The cholesteryl ester transfer protein I405V polymorphism is associated with increased high-density lipoprotein levels and decreased risk of myocardial infarction: the Rotterdam Study. European Journal of Preventive Cardiology. 14: 419-421. PMID 17568242 DOI: 10.1097/Hjr.0B013E32801101Aa  0.4
2007 Liu F, Arias-Vásquez A, Sleegers K, Aulchenko YS, Kayser M, Sanchez-Juan P, Feng BJ, Bertoli-Avella AM, van Swieten J, Axenovich TI, Heutink P, van Broeckhoven C, Oostra BA, van Duijn CM. A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population. American Journal of Human Genetics. 81: 17-31. PMID 17564960 DOI: 10.1086/518720  0.4
2007 Di Fonzo A, Chien HF, Socal M, Giraudo S, Tassorelli C, Iliceto G, Fabbrini G, Marconi R, Fincati E, Abbruzzese G, Marini P, Squitieri F, Horstink MW, Montagna P, Libera AD, ... ... Oostra BA, et al. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease. Neurology. 68: 1557-62. PMID 17485642 DOI: 10.1212/01.wnl.0000260963.08711.08  0.56
2007 Yazdanpanah M, Aulchenko YS, Hofman A, Janssen JAMJL, Sayed-Tabatabaei FA, Schaik RHNv, Klungel OH, Stricker BHCH, Pols HAP, Witteman JCM, Lamberts SWJ, Oostra BA, Duijn CMv. Effects of the Renin-Angiotensin System Genes and Salt Sensitivity Genes on Blood Pressure and Atherosclerosis in the Total Population and Patients With Type 2 Diabetes Diabetes. 56: 1905-1912. PMID 17446534 DOI: 10.2337/Db06-1127  0.4
2007 Isaacs A, Aulchenko YS, Hofman A, Sijbrands EJG, Sayed-Tabatabaei FA, Klungel OH, Zee AMd, Stricker BHC, Oostra BA, Witteman JCM, Duijn CMv. Epistatic effect of cholesteryl ester transfer protein and hepatic lipase on serum high-density lipoprotein cholesterol levels. The Journal of Clinical Endocrinology and Metabolism. 92: 2680-2687. PMID 17440012 DOI: 10.1210/Jc.2007-0269  0.4
2007 Isaacs A, Sayed-Tabatabaei FA, Aulchenko YS, Zillikens MC, Sijbrands EJ, Schut AF, Rutten WP, Pols HA, Witteman JC, Oostra BA, van Duijn CM. Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: the Erasmus Rucphen Family Study. European Journal of Epidemiology. 22: 99-105. PMID 17318336 DOI: 10.1007/s10654-006-9103-0  0.4
2007 Pauls D, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Scharf JM, Santangelo S, Stewart SE, Platko J, Pauls DL, Cox NJ, Robertson MM, Service S, ... ... Oostra BA, et al. Genome scan for tourette disorder in affected-sibling-pair and multigenerational families American Journal of Human Genetics. 80: 265-272. PMID 17304708 DOI: 10.1086/511052  0.56
2007 van Rijn MJ, Schut AF, Aulchenko YS, Deinum J, Sayed-Tabatabaei FA, Yazdanpanah M, Isaacs A, Axenovich TI, Zorkoltseva IV, Zillikens MC, Pols HA, Witteman JC, Oostra BA, van Duijn CM. Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes. Journal of Hypertension. 25: 565-70. PMID 17278972 DOI: 10.1097/HJH.0b013e32801449fb  0.4
2007 van Rijn MJ, Bos MJ, Isaacs A, Yazdanpanah M, Arias-Vásquez A, Stricker BH, Klungel OH, Oostra BA, Koudstaal PJ, Witteman JC, Hofman A, Breteler MM, van Duijn CM. Polymorphisms of the renin-angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathology. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 1083-7. PMID 17220293 DOI: 10.1136/Jnnp.2006.109819  0.4
2007 Grünewald A, Breedveld GJ, Lohmann-Hedrich K, Rohé CF, König IR, Hagenah J, Vanacore N, Meco G, Antonini A, Goldwurm S, Lesage S, Dürr A, Binkofski F, Siebner H, Münchau A, ... ... Oostra BA, et al. Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis. Neurogenetics. 8: 103-9. PMID 17219214 DOI: 10.1007/S10048-006-0072-Y  0.56
2006 Yazdanpanah M, Sayed-Tabatabaei FA, Hofman A, Aulchenko YS, Oostra BA, Stricker BHC, Pols HAP, Lamberts SWJ, Witteman JCM, Janssen JAMJL, Duijn CMv. The α-Adducin Gene Is Associated With Macrovascular Complications and Mortality in Patients With Type 2 Diabetes Diabetes. 55: 2922-2927. PMID 17003363 DOI: 10.2337/Db06-0302  0.4
2006 Verkerk AJ, Cath DC, van der Linde HC, Both J, Heutink P, Breedveld G, Aulchenko YS, Oostra BA. Genetic and clinical analysis of a large Dutch Gilles de la Tourette family. Molecular Psychiatry. 11: 954-64. PMID 16894393 DOI: 10.1038/sj.mp.4001877  0.56
2006 Despriet DDG, Klaver CCW, Witteman JCM, Bergen AAB, Kardys I, Maat MPMd, Boekhoorn SS, Vingerling JR, Hofman A, Oostra BA, Uitterlinden AG, Stijnen T, Duijn CMv, Jong PTVMd. Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration. Jama. 296: 301-309. PMID 16849663 DOI: 10.1001/Jama.296.3.301  0.36
2006 Brooks AS, Leegwater PA, Burzynski GM, Willems PJ, de Graaf B, van Langen I, Heutink P, Oostra BA, Hofstra RM, Bertoli-Avella AM. A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3 Journal of Medical Genetics. 43. PMID 16816022 DOI: 10.1136/jmg.2005.038125  0.56
2006 Sleegers K, de Koning I, Aulchenko YS, van Rijn MJ, Houben MP, Croes EA, van Swieten JC, Oostra BA, van Duijn CM. Cerebrovascular risk factors do not contribute to genetic variance of cognitive function: the ERF study. Neurobiology of Aging. 28: 735-41. PMID 16698126 DOI: 10.1016/j.neurobiolaging.2006.03.012  0.36
2006 Kardys I, Klaver CCW, Despriet DDG, Bergen AAB, Uitterlinden AG, Hofman A, Oostra BA, Duijn CMV, Jong PTVMd, Witteman JCM. A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study. Journal of the American College of Cardiology. 47: 1568-1575. PMID 16630992 DOI: 10.1016/J.Jacc.2005.11.076  0.36
2006 Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, et al. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nature Genetics. 38: 556-60. PMID 16582909 DOI: 10.1038/Ng1770  0.56
2006 Arias A, Isaacs A, Aulchenko Y, Hofman A, Breteler M, Oostra B, Duijn Cv. P1-309: Evidence for interaction between the Cholesteryl ester transfer protein (CETP) gene and APOE in late onset Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.687  0.36
2005 Sayed-Tabatabaei FA, van Rijn MJ, Schut AF, Aulchenko YS, Croes EA, Zillikens MC, Pols HA, Witteman JC, Oostra BA, van Duijn CM. Heritability of the function and structure of the arterial wall: findings of the Erasmus Rucphen Family (ERF) study. Stroke; a Journal of Cerebral Circulation. 36: 2351-6. PMID 16239631 DOI: 10.1161/01.STR.0000185719.66735.dd  0.4
2005 van Rijn MJ, Slooter AJ, Schut AF, Isaacs A, Aulchenko YS, Snijders PJ, Kappelle LJ, van Swieten JC, Oostra BA, van Duijn CM. Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population. Neurology. 65: 1203-9. PMID 16162858 DOI: 10.1212/01.wnl.0000178744.42953.b7  0.4
2005 Restivo L, Ferrari F, Passino E, Sgobio C, Bock J, Oostra BA, Bagni C, Ammassari-Teule M. Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome. Proceedings of the National Academy of Sciences of the United States of America. 102: 11557-62. PMID 16076950 DOI: 10.1073/Pnas.0504984102  0.56
2005 Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, Filla A, Farrer MJ, Bétard C, Singleton A, Hardy J, De Michele G, Bonifati V, Oostra BA, Gasser T, et al. Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 136: 72-4. PMID 15924299 DOI: 10.1002/Ajmg.B.30196  0.56
2005 Brooks AS, Bertoli-Avella AM, Burzynski GM, Breedveld GJ, Osinga J, Boven LG, Hurst JA, Mancini GM, Lequin MH, de Coo RF, Matera I, de Graaff E, Meijers C, Willems PJ, Tibboel D, ... Oostra BA, et al. Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems. American Journal of Human Genetics. 77: 120-6. PMID 15883926 DOI: 10.1086/431244  0.56
2005 Bertoli-Avella AM, Giroud-Benitez JL, Akyol A, Barbosa E, Schaap O, van der Linde HC, Martignoni E, Lopiano L, Lamberti P, Fincati E, Antonini A, Stocchi F, Montagna P, Squitieri F, Marini P, ... ... Oostra BA, et al. Novel parkin mutations detected in patients with early-onset Parkinson's disease Movement Disorders. 20: 424-431. PMID 15584030 DOI: 10.1002/mds.20343  0.56
2005 Pietrobono R, Tabolacci E, Zalfa F, Zito I, Terracciano A, Moscato U, Bagni C, Oostra B, Chiurazzi P, Neri G. Molecular dissection of the events leading to inactivation of the FMR1 gene. Human Molecular Genetics. 14: 267-77. PMID 15563507 DOI: 10.1093/Hmg/Ddi024  0.56
2004 Dekker MC, Eshuis SA, Maguire RP, Veenma-van der Duijn L, Pruim J, Snijders PJ, Oostra BA, van Duijn CM, Leenders KL. PET neuroimaging and mutations in the DJ-1 gene. Journal of Neural Transmission (Vienna, Austria : 1996). 111: 1575-81. PMID 15565491 DOI: 10.1007/S00702-004-0165-4  0.56
2004 Arias Vásquez A, Sleegers K, Dekker MC, van Gool WA, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM. A deletion in DJ-1 and the risk of dementia--a population-based survey. Neuroscience Letters. 372: 196-9. PMID 15542239 DOI: 10.1016/j.neulet.2004.09.040  0.56
2004 Stoyanova V, Rossetti S, Van Unen L, Oostra BA, Hoogeveen AT. Loss of FMR1 hypermethylation in somatic cell heterokaryons Faseb Journal. 18: 1964-1966. PMID 15377638 DOI: 10.1096/fj.04-2499fje  0.56
2004 Sleegers K, Roks G, Theuns J, Aulchenko YS, Rademakers R, Cruts M, van Gool WA, Van Broeckhoven C, Heutink P, Oostra BA, van Swieten JC, van Duijn CM. Familial clustering and genetic risk for dementia in a genetically isolated Dutch population. Brain : a Journal of Neurology. 127: 1641-9. PMID 15130954 DOI: 10.1093/brain/awh179  0.56
2004 Willemsen R, Oostra BA, Bassell GJ, Dictenberg J. The fragile X syndrome: from molecular genetics to neurobiology. Mental Retardation and Developmental Disabilities Research Reviews. 10: 60-7. PMID 14994290 DOI: 10.1002/mrdd.20010  0.56
2003 Aulchenko YS, Vaessen N, Heutink P, Pullen J, Snijders PJLM, Hofman A, Sandkuijl LA, Houwing-Duistermaat JJ, Edwards M, Bennett S, Oostra BA, Duijn CMv. A Genome-Wide Search for Genes Involved in Type 2 Diabetes in a Recently Genetically Isolated Population From the Netherlands Diabetes. 52: 3001-3004. PMID 14633863 DOI: 10.2337/Diabetes.52.12.3001  0.36
2003 Dekker MC, van Swieten JC, Houwing-Duistermaat JJ, Snijders PJ, Boeren E, Hofman A, Breteler MM, Heutink P, Oostra BA, van Duijn CM. A clinical-genetic study of Parkinson's disease in a genetically isolated community. Journal of Neurology. 250: 1056-62. PMID 14504966 DOI: 10.1007/S00415-003-0151-Z  0.36
2003 Lettice LA, Heaney SJ, Purdie LA, Li L, de Beer P, Oostra BA, Goode D, Elgar G, Hill RE, de Graaff E. A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly. Human Molecular Genetics. 12: 1725-35. PMID 12837695 DOI: 10.1093/Hmg/Ddg180  0.56
2003 Verkerk AJMH, Mathews CA, Joosse M, Eussen BHJ, Heutink P, Oostra BA. CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder Genomics. 82: 1-9. PMID 12809671 DOI: 10.1016/S0888-7543(03)00097-1  0.56
2003 Schut AF, Janssen JA, Deinum J, Vergeer JM, Hofman A, Lamberts SW, Oostra BA, Pols HA, Witteman JC, van Duijn CM. Polymorphism in the promoter region of the insulin-like growth factor I gene is related to carotid intima-media thickness and aortic pulse wave velocity in subjects with hypertension. Stroke; a Journal of Cerebral Circulation. 34: 1623-7. PMID 12791939 DOI: 10.1161/01.STR.0000076013.00240.B0  0.4
2003 Zalfa F, Giorgi M, Primerano B, Moro A, Di Penta A, Reis S, Oostra B, Bagni C. The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses. Cell. 112: 317-27. PMID 12581522 DOI: 10.1016/S0092-8674(03)00079-5  0.56
2002 Valente EM, Brancati F, Caputo V, Graham EA, Davis MB, Ferraris A, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Filla A, Meco G, ... Oostra BA, et al. PARK6 is a common cause of familial parkinsonism. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 23: S117-8. PMID 12548371 DOI: 10.1007/S100720200097  0.56
2002 Irwin SA, Idupulapati M, Gilbert ME, Harris JB, Chakravarti AB, Rogers EJ, Crisostomo RA, Larsen BP, Mehta A, Alcantara CJ, Patel B, Swain RA, Weiler IJ, Oostra BA, Greenough WT. Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice. American Journal of Medical Genetics. 111: 140-6. PMID 12210340 DOI: 10.1002/Ajmg.10500  0.56
2002 Willemsen R, Bontekoe CJ, Severijnen LA, Oostra BA. Timing of the absence of FMR1 expression in full mutation chorionic villi. Human Genetics. 110: 601-5. PMID 12107447 DOI: 10.1007/s00439-002-0723-5  0.56
2002 Mineur YS, Sluyter F, de Wit S, Oostra BA, Crusio WE. Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse. Hippocampus. 12: 39-46. PMID 11918286 DOI: 10.1002/hipo.10005  0.56
2002 Bontekoe CJ, McIlwain KL, Nieuwenhuizen IM, Yuva-Paylor LA, Nellis A, Willemsen R, Fang Z, Kirkpatrick L, Bakker CE, McAninch R, Cheng NC, Merriweather M, Hoogeveen AT, Nelson D, Paylor R, ... Oostra BA, et al. Knockout mouse model for Fxr2: a model for mental retardation. Human Molecular Genetics. 11: 487-98. PMID 11875043 DOI: 10.1093/Hmg/11.5.487  0.56
2002 Valente EM, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Wassilowsky D, Harhangi BS, Rawal N, ... ... Oostra BA, et al. PARK6-linked parkinsonism occurs in several European families. Annals of Neurology. 51: 14-8. PMID 11782979 DOI: 10.1002/Ana.10053  0.56
2001 Bontekoe CJ, Bakker CE, Nieuwenhuizen IM, van der Linde H, Lans H, de Lange D, Hirst MC, Oostra BA. Instability of a (CGG)98 repeat in the Fmr1 promoter. Human Molecular Genetics. 10: 1693-9. PMID 11487573 DOI: 10.1093/HMG/10.16.1693  0.56
2001 Bonifati V, De Michele G, Lücking CB, Dürr A, Fabrizio E, Ambrosio G, Vanacore N, De Mari M, Marconi R, Capus L, Breteler MM, Gasser T, Oostra B, Wood N, Agid Y, et al. The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 22: 51-2. PMID 11487197 DOI: 10.1007/S100720170042  0.56
2000 Van Dam D, D'Hooge R, Hauben E, Reyniers E, Gantois I, Bakker CE, Oostra BA, Kooy RF, De Deyn PP. Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice. Behavioural Brain Research. 117: 127-36. PMID 11099766 DOI: 10.1016/S0166-4328(00)00296-5  0.56
2000 Bakker CE, de Diego Otero Y, Bontekoe C, Raghoe P, Luteijn T, Hoogeveen AT, Oostra BA, Willemsen R. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse. Experimental Cell Research. 258: 162-70. PMID 10912798 DOI: 10.1006/excr.2000.4932  0.56
2000 Tamanini F, Kirkpatrick LL, Schonkeren J, van Unen L, Bontekoe C, Bakker C, Nelson DL, Galjaard H, Oostra BA, Hoogeveen AT. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins. Human Molecular Genetics. 9: 1487-93. PMID 10888599 DOI: 10.1093/hmg/9.10.1487  0.56
2000 Bakker CE, Kooy RF, D'Hooge R, Tamanini F, Willemsen R, Nieuwenhuizen I, De Vries BBA, Reyniers E, Hoogeveen AT, Willems PJ, De Deyn PP, Oostra BA. Introduction of a FMR1 transgene in the fragile X knockout mouse Neuroscience Research Communications. 26: 265-277. DOI: 10.1002/1520-6769(200005/06)26:3<265::Aid-Nrc13>3.0.Co;2-T  0.56
1999 Froelich S, Houlden H, Rizzu P, Chakraverty S, Baker M, Kwon J, Nowotny P, Isaacs A, Nowotny V, Wauters E, van Baren MJ, Oostra BA, Hardy J, Lannfelt L, Goate A, et al. Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21. Genomics. 60: 129-36. PMID 10486204 DOI: 10.1006/Geno.1999.5892  0.56
1999 Reyniers E, Martin JJ, Cras P, Van Marck E, Handig I, Jorens HZ, Oostra BA, Kooy RF, Willems PJ. Postmortem examination of two fragile X brothers with an FMR1 full mutation. American Journal of Medical Genetics. 84: 245-9. PMID 10331601 DOI: 10.1002/(Sici)1096-8628(19990528)84:3<245::Aid-Ajmg16>3.0.Co;2-U  0.56
1999 Tamanini F, Bontekoe C, Bakker CE, van Unen L, Anar B, Willemsen R, Yoshida M, Galjaard H, Oostra BA, Hoogeveen AT. Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations. Human Molecular Genetics. 8: 863-9. PMID 10196376 DOI: 10.1093/HMG/8.5.863  0.56
1999 Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. American Journal of Human Genetics. 64: 414-21. PMID 9973279 DOI: 10.1086/302256  0.56
1998 Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, Scheltens P, Ravid R, Oostra BA, Niermeijer MF, van Swieten JC. Familial aggregation in frontotemporal dementia. Neurology. 50: 1541-5. PMID 9633692  0.56
1998 D'Adamo P, Menegon A, Lo Nigro C, Grasso M, Gulisano M, Tamanini F, Bienvenu T, Gedeon AK, Oostra B, Wu SK, Tandon A, Valtorta F, Balch WE, Chelly J, Toniolo D. Mutations in GDI1 are responsible for X-linked non-specific mental retardation. Nature Genetics. 19: 134-9. PMID 9620768 DOI: 10.1038/487  0.56
1998 Steward O, Bakker CE, Willems PJ, Oostra BA. No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome. Neuroreport. 9: 477-81. PMID 9512393 DOI: 10.1097/00001756-199802160-00022  0.56
1998 Storm K, Handig I, Reyniers E, Oostra BA, Kooy RF, Willems PJ. Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome. Human Genetics. 102: 54-6. PMID 9490298 DOI: 10.1007/s004390050653  0.56
1997 Losekoot M, Hoogendoorn E, Olmer R, Jansen CC, Oosterwijk JC, van den Ouweland AM, Halley DJ, Warren ST, Willemsen R, Oostra BA, Bakker E. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. Journal of Medical Genetics. 34: 924-6. PMID 9391887 DOI: 10.1136/Jmg.34.11.924  0.56
1997 Tamanini F, Willemsen R, van Unen L, Bontekoe C, Galjaard H, Oostra BA, Hoogeveen AT. Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis. Human Molecular Genetics. 6: 1315-22. PMID 9259278 DOI: 10.1093/hmg/6.8.1315  0.56
1997 Schwemmle S, de Graaff E, Deissler H, Gläser D, Wöhrle D, Kennerknecht I, Just W, Oostra BA, Döerfler W, Vogel W, Steinbach P, Dörfler W. Characterization of FMR1 promoter elements by in vivo-footprinting analysis. American Journal of Human Genetics. 60: 1354-62. PMID 9199556 DOI: 10.1086/515456  0.56
1997 Comery TA, Harris JB, Willems PJ, Oostra BA, Irwin SA, Weiler IJ, Greenough WT. Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits. Proceedings of the National Academy of Sciences of the United States of America. 94: 5401-4. PMID 9144249 DOI: 10.1073/Pnas.94.10.5401  0.56
1997 Malter HE, Iber JC, Willemsen R, De Graaff E, Tarleton JC, Leisti J, Warren ST, Oostra BA. Characterization of the full fragile X syndrome mutation in fetal gametes Nature Genetics. 15: 165-169. PMID 9020841 DOI: 10.1038/Ng0297-165  0.56
1996 Newport MJ, Huxley CM, Huston S, Hawrylowicz CM, Oostra BA, Williamson R, Levin M. A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection. The New England Journal of Medicine. 335: 1941-9. PMID 8960473 DOI: 10.1056/Nejm199612263352602  0.56
1996 Willemsen R, Bontekoe C, Tamanini F, Galjaard H, Hoogeveen A, Oostra B. Association of FMRP with ribosomal precursor particles in the nucleolus. Biochemical and Biophysical Research Communications. 225: 27-33. PMID 8769090 DOI: 10.1006/bbrc.1996.1126  0.56
1996 Shimizu M, Gellibolian R, Oostra BA, Wells RD. Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene. Journal of Molecular Biology. 258: 614-26. PMID 8636996 DOI: 10.1006/Jmbi.1996.0273  0.56
1995 Hendriksen PJM, Hoogerbrugge JW, Themmen APN, Koken MHM, Hoeijmakers JHJ, Oostra BA, Van Der Lende T, Grootegoed JA. Postmeiotic transcription of X and Y chromosomal genes during spermatogenesis in the mouse Developmental Biology. 170: 730-733. PMID 7649399 DOI: 10.1006/dbio.1995.1252  0.56
1995 Bosma PJ, Chowdhury JR, Bakker C, Gantla S, De Boer A, Oostra BA, Lindhout D, Tytgat GNJ, Jansen PLM, Elferink RPJO, Chowdhury NR. The genetic basis of the reduced expression of bilirubin UDP- glucuronosyltransferase 1 in Gilbert's syndrome New England Journal of Medicine. 333: 1171-1175. PMID 7565971 DOI: 10.1056/NEJM199511023331802  0.56
1994 The Dutch-Belgian Fragile X Consorthium, Bakker CE, Verheij C, Willemsen R, van der Helm R, Oerlemans F, Vermey M, Bygrave A, Hoogeveen A, Oostra BA, Reyniers E, De Boule K, D'Hooge R, Cras P, van Velzen D, et al. Fmr1 knockout mice: A model to study fragile X mental retardation Cell. 78: 23-33. PMID 8033209 DOI: 10.1016/0092-8674(94)90569-X  0.56
1994 Chiurazzi P, de Graaff E, Ng J, Verkerk AJ, Wolfson S, Fisch GS, Kozak L, Neri G, Oostra BA. No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. American Journal of Medical Genetics. 51: 309-14. PMID 7942992 DOI: 10.1002/ajmg.1320510405  0.56
1994 Heutink P, Haitjema T, Breedveld GJ, Janssen B, Sandkuijl LA, Bontekoe CJ, Westerman CJ, Oostra BA. Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity. Journal of Medical Genetics. 31: 933-6. PMID 7891375 DOI: 10.1136/jmg.31.12.933  0.56
1994 Ouweland AMwVD, Deelen WH, Kunst CB, Uzielli MLG, Nelson DL, Warren ST, Oostra BA, Halley DJJ. Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes Human Molecular Genetics. 3: 1823-1827. PMID 7849707 DOI: 10.1093/Hmg/3.10.1823  0.56
1993 Richards FM, Maher ER, Latif F, Phipps ME, Tory K, Lush M, Crossey PA, Oostra B, Enblad P, Gustavson KH. Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene. Journal of Medical Genetics. 30: 104-7. PMID 8445612 DOI: 10.1136/jmg.30.2.104  0.56
1992 Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Intragenic probe used for diagnostics in fragile X families. American Journal of Medical Genetics. 43: 192-6. PMID 1605192 DOI: 10.1002/Ajmg.1320430132  0.56
1991 Pieretti M, Zhang FP, Fu YH, Warren ST, Oostra BA, Caskey CT, Nelson DL. Absence of expression of the FMR-1 gene in fragile X syndrome. Cell. 66: 817-22. PMID 1878973 DOI: 10.1016/0092-8674(91)90125-I  0.56
1991 Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RG, Warren ST. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell. 67: 1047-58. PMID 1760838 DOI: 10.1016/0092-8674(91)90283-5  0.56
1991 Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 65: 905-14. PMID 1710175 DOI: 10.1016/0092-8674(91)90397-H  0.56
1990 Devor EJ, Grandy DK, Civelli O, Litt M, Burgess AK, Isenberg KE, van de Wetering BJ, Oostra B. Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome. Human Heredity. 40: 105-8. PMID 2335364 DOI: 10.1159/000153914  0.56
1990 Dean M, Amos JA, Lynch J, Romeo G, Devoto M, Ward K, Halley D, Oostra B, Ferrari M, Russo S. Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8. Human Genetics. 85: 275-8. PMID 1975555 DOI: 10.1007/Bf00206745  0.56
1988 Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Farmer GE, Lamiell JM, Haines J, Yuen JW, Collins D, Majoor-Krakauer D. Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma. Nature. 332: 268-9. PMID 2894613 DOI: 10.1038/332268A0  0.56
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