Common variants at 6q22 and 17q21 are associated with intracranial volume
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Wiro J Niessen | Clifford R Jack | Reinhold Schmidt | Stefan Ropele | Sudha Seshadri | Nicholas J Timpson | Vilmundur Gudnason | Tamara B Harris | Mark I McCarthy | Fernando Rivadeneira | Aad van der Lugt | David S Knopman | Albert Hofman | Cornelia M van Duijn | Joachim Heinrich | Hakon Hakonarson | Rhoda Au | Lenore J Launer | Myriam Fornage | Anita L DeStefano | Helena Schmidt | Vincent W V Jaddoe | Lyle J Palmer | Haukur Gudnason | Alex P Zijdenbos | Maksim Struchalin | Anna-Liisa Hartikainen | M Arfan Ikram | Diane Catellier | Marjo-Riitta Jarvelin | Sigurdur Sigurdsson | George Davey Smith | M. Jarvelin | L. Coin | M. Fornage | M. Nalls | A. Hofman | A. Uitterlinden | I. Ntalla | M. McCarthy | E. Zeggini | D. Strachan | D. Lawlor | T. Lehtimäki | H. Hakonarson | D. Hadley | S. Grant | C. Jack | C. Lindgren | J. Hirschhorn | P. Wolf | N. Timpson | Y. Teo | V. Gudnason | Albert Vernon Smith | A. Lewin | F. Rivadeneira | L. Palmer | D. Knopman | A. Zijdenbos | U. Sovio | W. Niessen | G. Willemsen | K. Mohlke | O. Simell | T. Harris | T. Lakka | H. Lakka | M. van Buchem | D. Boomsma | S. Ropele | J. Heinrich | M. Horikoshi | C. V. van Duijn | C. Power | R. Schmidt | H. Vrooman | M. Breteler | H. Schmidt | M. Vernooij | M. Ikram | R. Au | K. Ong | A. Hinney | O. Davis | K. Benke | G. Dedoussis | M. Kowgier | L. Launer | B. St Pourcain | G. Smith | S. Saw | A. DeStefano | T. Mosley | S. Seshadri | T. Kilpeläinen | D. Mook-Kanamori | M. Atalay | A. Hartikainen | C. DeCarli | V. Jaddoe | E. Steegers | R. Salem | S. Debette | A. Scherag | E. Hypponen | S. Sebert | L. Lange | C. Pennell | E. Thiering | C. Middeldorp | Alexa Beiser | S. Sigurdsson | D. Catellier | W. Longstreth | B. Pourcain | C. Holst | A. van der Lugt | K. Panoutsopoulou | V. Lindi | M. Nivard | B. Valcárcel | E. Oken | W. Ang | E. Nøhr | C. Haworth | B. Hocher | M. Kirin | I. Millwood | Alina Rodriguez | Haukur Gudnason | Liang Goh | M. Struchalin | M. Groen-Blokhuis | B. Windham | R. Gaillard | V. Huikari | C. Flexeder | Jouke Jan Hottenga | H. R. Taal | D. Berry | L. Coker | Philip A Wolf | Albert V Smith | Andre G Uitterlinden | T. V. van Beijsterveldt | Mark A van Buchem | Eric A P Steegers | Meike W Vernooij | Mike A Nalls | Craig E Pennell | Elisabeth Thiering | Thomas H Mosley | Stéphanie Debette | Monique M B Breteler | Ulla Sovio | Struan F A Grant | Beate St Pourcain | Charles DeCarli | Dennis O Mook-Kanamori | Laura H Coker | W. M. Meeks | W T Longstreth | H Rob Taal | Henri A Vrooman | B Gwen Windham | Alexa Beiser | William M Meeks | J. Holloway | A. Smith | C. Cooper | O. Raitakari | J. Murray | N. Siitonen | Linda S. Adair | N. Bergen | Paul Elliott | T. Frayling | M Arfan Myriam Albert V Sudha Reinhold Stéphanie Hen Ikram Fornage Smith Seshadri Schmidt Debette Vr | Linda S Wei Mustafa Toos Nienke Kelly Diane Lachlan Oliv Adair Ang Atalay van Beijsterveldt Bergen B | Johannes Hedebrand | Reedik Maggi | Julie K. Marsh | Jennifer Pararajasingham | Matthew Gillman | Ewan R Pearson | Thomas S. Price | James F. Wilson | A. Smith | J. C. Murray | A. Uitterlinden | W. Meeks | J. Heinrich | A. Hofman | C. V. van Duijn | D. Boomsma | M. McCarthy | A. Destefano | Olli T. Raitakari | R. Schmidt | M. McCarthy | D. Knopman | R. Schmidt | P. Elliott | B. S. Pourcain | H. Taal
[1] K. Johnson. An Update. , 1984, Journal of food protection.
[2] R. Pfundt,et al. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism , 2006, Nature Genetics.
[3] P. Allhoff,et al. The Framingham Offspring Study , 1991 .
[4] Sudha Seshadri,et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. , 2010, JAMA.
[5] J. Stevens,et al. The Atherosclerosis Risk in Communities Study , 2013 .
[6] H. Braak,et al. Molecular evolution and genetics of the Saitohin gene and tau haplotype in Alzheimer's disease and argyrophilic grain disease , 2004, Journal of neurochemistry.
[7] Ayellet V. Segrè,et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height , 2010, Nature.
[8] C. Broeckhoven,et al. Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update , 2008, Human mutation.
[9] Jong Jin Kim,et al. The distribution and most recent common ancestor of the 17q21 inversion in humans. , 2010, American journal of human genetics.
[10] Josephine C. Adams,et al. The thrombospondin type 1 repeat (TSR) superfamily: Diverse proteins with related roles in neuronal development , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.
[11] Charles DeCarli,et al. Genetic Variation in White Matter Hyperintensity Volume in the Framingham Study , 2004, Stroke.
[12] G. Roth,et al. Evolution of the brain and intelligence , 2005, Trends in Cognitive Sciences.
[13] Joseph T. Glessner,et al. A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene , 2007, Nature.
[14] Wiro J. Niessen,et al. Brain tissue volumes in the general elderly population The Rotterdam Scan Study , 2008, Neurobiology of Aging.
[15] D. Harvey,et al. Measures of brain morphology and infarction in the framingham heart study: establishing what is normal , 2005, Neurobiology of Aging.
[16] B L Miller,et al. Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins. , 1998, Stroke.
[17] A. Hofman,et al. Incidental findings on brain MRI in the general population. , 2007, The New England journal of medicine.
[18] D. Reich,et al. Principal components analysis corrects for stratification in genome-wide association studies , 2006, Nature Genetics.
[19] K. Lunetta,et al. Methods in Genetics and Clinical Interpretation Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Design of Prospective Meta-Analyses of Genome-Wide Association Studies From 5 Cohorts , 2010 .
[20] Christopher N Martyn,et al. The Influence of Head Growth in Fetal Life, Infancy, and Childhood on Intelligence at the Ages of 4 and 8 Years , 2006, Pediatrics.
[21] C. Jack,et al. FLAIR histogram segmentation for measurement of leukoaraiosis volume , 2001, Journal of magnetic resonance imaging : JMRI.
[22] K. Godfrey,et al. Critical periods of brain growth and cognitive function in children. , 2004, Brain : a journal of neurology.
[23] C. Broeckhoven,et al. Progranulin locus deletion in frontotemporal dementia , 2008, Human mutation.
[24] P. Amouyel,et al. Association of polymorphisms in the Tau and Saitohin genes with Parkinson’s disease , 2004, Journal of Neurology, Neurosurgery & Psychiatry.
[25] C. Hoggart,et al. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population , 2008, Nature Genetics.
[26] H. Wichmann,et al. Associations between BMI and the FTO Gene Are Age Dependent: Results from the GINI and LISA Birth Cohort Studies up to Age 6 Years , 2010, Obesity Facts.
[27] R. Nitsch,et al. The novel cytosolic RING finger protein dactylidin is up‐regulated in brains of patients with Alzheimer's disease , 2005, The European journal of neuroscience.
[28] A. Hofman,et al. The Generation R Study: design and cohort update until the age of 4 years , 2008, European Journal of Epidemiology.
[29] H. Stefánsson,et al. A common inversion under selection in Europeans , 2005, Nature Genetics.
[30] W. Pan,et al. Corticotropin-releasing hormone receptor-1 in cerebral microvessels changes during development and influences urocortin transport across the blood-brain barrier. , 2010, Endocrinology.
[31] J. Geddes,et al. What is a randomised controlled trial? , 2009, Epidemiologia e Psichiatria Sociale.
[32] Zhaoshi Jiang,et al. Evolutionary toggling of the MAPT 17q21.31 inversion region , 2008, Nature Genetics.
[33] F. Fazekas,et al. MRI cerebral white matter lesions and paraoxonase PON1 polymorphisms : three-year follow-up of the austrian stroke prevention study. , 2000, Arteriosclerosis, thrombosis, and vascular biology.
[34] W. Markesbery,et al. Head Circumference, Education and Risk of Dementia: Findings from the Nun Study , 2003, Journal of clinical and experimental neuropsychology.
[35] M. Pembrey,et al. ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology. , 2001, Paediatric and perinatal epidemiology.
[36] Aad van der Lugt,et al. Common variants at 12q15 and 12q24 are associated with infant head circumference , 2012, Nature Genetics.
[37] Ricardo J Komotar,et al. Genomewide Association Studies of Stroke. , 2009, Neurosurgery.
[38] Wiro J. Niessen,et al. Multi-spectral brain tissue segmentation using automatically trained k-Nearest-Neighbor classification , 2007, NeuroImage.
[39] Wiro J. Niessen,et al. The Rotterdam Scan Study: design and update up to 2012 , 2011, European Journal of Epidemiology.
[40] D. Galimberti,et al. The H1 haplotype of the tau gene (MAPT) is associated with mild cognitive impairment. , 2010, Journal of Alzheimer's disease : JAD.
[41] L. Vissers,et al. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome , 2008, Journal of Medical Genetics.