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Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities

N. Armstrong, K. Mather, M. Sargurupremraj, M. Knol, R. Malik, C. Satizabal, L. Yanek, W. Wen, V. Gudnason, N. Dueker, L. Elliott, E. Hofer, J. Bis, N. Jahanshad, S. Li, M. Logue, M. Luciano, M. Scholz, A. Smith, S. Trompet, D. Vojinovic, R. Xia, F. Alfaro-Almagro, D. Ames, N. Amin, P. Amouyel, A. Beiser, H. Brodaty, I. Deary, C. Fennema-Notestine, P. Gampawar, R. Gottesman, L. Griffanti, C. Jack, Jr, M. Jenkinson, J. Jiang, B. Kral, J. Kwok, L. Lampe, D. C M Liewald, P. Maillard, J. Marchini, M. Bastin, B. Mazoyer, L. Pirpamer, J. Rafael Romero, G. Roshchupkin, P. Schofield, M. Schroeter, D. Stott, A. Thalamuthu, J. Trollor, C. Tzourio, J. van der Grond, M. Vernooij, V. Witte, M. Wright, Q. Yang, Z. Morris, S. Siggurdsson, B. Psaty, A. Villringer, H. Schmidt, A. Haberg, C. van Duijn, J. Jukema, M. Dichgans, R. Sacco, C. Wright, W. Kremen, L. Becker, P. Thompson, T. Mosley, J. Wardlaw, M. Ikram, H. Adams, S. Seshadri, P. Sachdev, S. Smith, L. Launer, W. Longstreth, C. DeCarli, R. Schmidt, M. Fornage, S. Debette, and P. Nyquist. Stroke, 51 (7): 2111--2121 (July 2020)

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Global and regional development of the human cerebral cortex: Molecular architecture and occupational aptitudesJ. Shin, S. Ma, E. Hofer, Y. Patel, D. Vosberg, S. Tilley, G. Roshchupkin, A. Sousa, X. Jian, R. Gottesman and 60 other author(s). Cereb. Cortex, 30 (7): 4121--4139 (June 2020)GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomesN. Franceschini, C. Giambartolomei, P. de Vries, C. Finan, J. Bis, R. Huntley, R. Lovering, S. Tajuddin, T. Winkler, M. Graff and 149 other author(s). Nat. Commun., 9 (1): 5141 (December 2018)Genetic architecture of subcortical brain structures in 38,851 individualsC. Satizabal, H. Adams, D. Hibar, C. White, M. Knol, J. Stein, M. Scholz, M. Sargurupremraj, N. Jahanshad, G. Roshchupkin and 279 other author(s). Nat. Genet., 51 (11): 1624--1636 (November 2019)Meta-analysis uncovers genome-wide significant variants for rapid kidney function declineM. Gorski, B. Jung, Y. Li, P. Matias-Garcia, M. Wuttke, S. Coassin, C. Thio, M. Kleber, T. Winkler, V. Wanner and 169 other author(s). Kidney International, 99 (4): 926--939 (2021)Meta-analysis uncovers genome-wide significant variants for rapid kidney function declineM. Gorski, B. Jung, Y. Li, P. Matias-Garcia, M. Wuttke, S. Coassin, C. Thio, M. Kleber, T. Winkler, V. Wanner and 123 other author(s). Kidney Int., 99 (4): 926--939 (April 2021)Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adultsE. Hofer, G. Roshchupkin, H. Adams, M. Knol, H. Lin, S. Li, H. Zare, S. Ahmad, N. Armstrong, C. Satizabal and 90 other author(s). Nat. Commun., 11 (1): 4796 (September 2020)A catalog of genetic loci associated with kidney function from analyses of a million individualsM. Wuttke, Y. Li, M. Li, K. Sieber, M. Feitosa, M. Gorski, A. Tin, L. Wang, A. Chu, A. Hoppmann and 319 other author(s). Nat. Genet., 51 (6): 957--972 (June 2019)Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volumeD. Vojinovic, H. Adams, X. Jian, Q. Yang, A. Smith, J. Bis, A. Teumer, M. Scholz, N. Armstrong, E. Hofer and 81 other author(s). Nat. Commun., 9 (1): 3945 (September 2018)Target genes, variants, tissues and transcriptional pathways influencing human serum urate levelsA. Tin, J. Marten, V. Halperin Kuhns, Y. Li, M. Wuttke, H. Kirsten, K. Sieber, C. Qiu, M. Gorski, Z. Yu and 218 other author(s). Nat. Genet., 51 (10): 1459--1474 (October 2019)Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive functionG. Davies, M. Lam, S. Harris, J. Trampush, M. Luciano, W. Hill, S. Hagenaars, S. Ritchie, R. Marioni, C. Fawns-Ritchie and 212 other author(s). Nat. Commun., (May 2018)

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Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities

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Disambiguation of "Schmidt, Reinhold"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities

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Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities