Author of the publication

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

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)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

No persons found for author name Yang, Qiong

add a person with the name Yang, Qiong

Other publications of authors with the same name

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)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)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 und 81 andere Autor(en). Nat. Commun., 9 (1): 3945 (September 2018)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 und 169 andere Autor(en). Kidney International, 99 (4): 926--939 (2021)Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaA. Teumer, Y. Li, S. Ghasemi, B. Prins, M. Wuttke, T. Hermle, A. Giri, K. Sieber, C. Qiu, H. Kirsten und 176 andere Autor(en). Nat. Commun., 10 (1): 4130 (September 2019)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 und 279 andere Autor(en). Nat. Genet., 51 (11): 1624--1636 (November 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 und 212 andere Autor(en). Nat. Commun., (May 2018)Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensitiesN. Armstrong, K. Mather, M. Sargurupremraj, M. Knol, R. Malik, C. Satizabal, L. Yanek, W. Wen, V. Gudnason, N. Dueker und 76 andere Autor(en). Stroke, 51 (7): 2111--2121 (July 2020)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 und 90 andere Autor(en). 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 und 319 andere Autor(en). Nat. Genet., 51 (6): 957--972 (June 2019)

PUMA

Disambiguation of "Yang, Qiong"

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

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

Please choose a person to relate this publication to

Other publications of authors with the same name

Disambiguierung

PUMA

Disambiguation of "Yang, Qiong"

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

Please choose a person to relate this publication to

Other publications of authors with the same name

Disambiguierung

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

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