![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 2
2025
Georgakis, Marios K. 
ORCID: https://orcid.org/0000-0003-3507-3659; Malik, Rainer ORCID: https://orcid.org/0000-0001-9212-2520; El Bounkari, Omar ORCID: https://orcid.org/0000-0002-3051-2096; Hasbani, Natalie R.; Li, Jiang; Huffman, Jennifer E.; Shakt, Gabrielle; Tack, Reinier W. P.; Kimball, Tamara N.; Asare, Yaw ORCID: https://orcid.org/0000-0002-8946-5650; Morrison, Alanna C.; Tsao, Noah L.; Judy, Renae; Mitchell, Braxton D.; Xu, Huichun; Montasser, May E.; Do, Ron; Kenny, Eimear E.; Loos, Ruth J. F.; Terry, James G.; Carr, John Jeffrey; Bis, Joshua C.; Psaty, Bruce M.; Longstreth, W. T.; Young, Kendra A.; Lutz, Sharon M.; Cho, Michael H.; Broome, Jai; Khan, Alyna T.; Wang, Fei Fei; Heard-Costa, Nancy; Seshadri, Sudha; Vasan, Ramachandran S.; Palmer, Nicholette D.; Freedman, Barry I.; Bowden, Donald W.; Yanek, Lisa R.; Kral, Brian G.; Becker, Lewis C.; Peyser, Patricia A.; Bielak, Lawrence F.; Ammous, Farah; Carson, April P.; Hall, Michael E.; Raffield, Laura M.; Rich, Stephen S.; Post, Wendy S.; Tracy, Russel P.; Taylor, Kent D.; Guo, Xiuqing; Mahaney, Michael C.; Curran, Joanne E.; Blangero, John; Clarke, Shoa L.; Haessler, Jeffrey W.; Hu, Yao; Assimes, Themistocles L.; Kooperberg, Charles; Bernhagen, Jürgen ORCID: https://orcid.org/0000-0003-2996-2652; Anderson, Christopher D.; Damrauer, Scott M.; Zand, Ramin; Rotter, Jerome I.; Vries, Paul S. de und Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X
(2025):
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.
In: Genome Medicine, Bd. 17, 27
[PDF, 2MB]
ORCID: https://orcid.org/0000-0003-3507-3659; Malik, Rainer ORCID: https://orcid.org/0000-0001-9212-2520; El Bounkari, Omar ORCID: https://orcid.org/0000-0002-3051-2096; Hasbani, Natalie R.; Li, Jiang; Huffman, Jennifer E.; Shakt, Gabrielle; Tack, Reinier W. P.; Kimball, Tamara N.; Asare, Yaw ORCID: https://orcid.org/0000-0002-8946-5650; Morrison, Alanna C.; Tsao, Noah L.; Judy, Renae; Mitchell, Braxton D.; Xu, Huichun; Montasser, May E.; Do, Ron; Kenny, Eimear E.; Loos, Ruth J. F.; Terry, James G.; Carr, John Jeffrey; Bis, Joshua C.; Psaty, Bruce M.; Longstreth, W. T.; Young, Kendra A.; Lutz, Sharon M.; Cho, Michael H.; Broome, Jai; Khan, Alyna T.; Wang, Fei Fei; Heard-Costa, Nancy; Seshadri, Sudha; Vasan, Ramachandran S.; Palmer, Nicholette D.; Freedman, Barry I.; Bowden, Donald W.; Yanek, Lisa R.; Kral, Brian G.; Becker, Lewis C.; Peyser, Patricia A.; Bielak, Lawrence F.; Ammous, Farah; Carson, April P.; Hall, Michael E.; Raffield, Laura M.; Rich, Stephen S.; Post, Wendy S.; Tracy, Russel P.; Taylor, Kent D.; Guo, Xiuqing; Mahaney, Michael C.; Curran, Joanne E.; Blangero, John; Clarke, Shoa L.; Haessler, Jeffrey W.; Hu, Yao; Assimes, Themistocles L.; Kooperberg, Charles; Bernhagen, Jürgen ORCID: https://orcid.org/0000-0003-2996-2652; Anderson, Christopher D.; Damrauer, Scott M.; Zand, Ramin; Rotter, Jerome I.; Vries, Paul S. de und Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X
(2025):
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.
In: Genome Medicine, Bd. 17, 27
[PDF, 2MB]
2020
Armstrong, Nicola J.; Mather, Karen A.; Sargurupremraj, Muralidharan; Knol, Maria J.; Malik, Rainer; Satizabal, Claudia L.; Yanek, Lisa R.; Wen, Wei; Gudnason, Vilmundur G.; Dueker, Nicole D.; Elliott, Lloyd T.; Hofer, Edith; Bis, Joshua; Jahanshad, Neda; Li, Shuo; Logue, Mark A.; Luciano, Michelle; Scholz, Markus; Smith, Albert V.; Trompet, Stella; Vojinovic, Dina; Xia, Rui; Alfaro-Almagro, Fidel; Ames, David; Amin, Najaf; Amouyel, Philippe; Beiser, Alexa S.; Brodaty, Henry; Deary, Ian J.; Fennema-Notestine, Christine; Gampawar, Piyush G.; Gottesman, Rebecca; Griffanti, Ludovica; Jack, Clifford R.; Jenkinson, Mark; Jiang, Jiyang; Kral, Brian G.; Kwok, John B.; Lampe, Leonie; Liewald, David C. M.; Maillard, Pauline; Marchini, Jonathan; Bastin, Mark E.; Mazoyer, Bernard; Pirpamer, Lukas; Rafael Romero, Jose; Roshchupkin, Gennady V.; Schofield, Peter R.; Schroeter, Matthias L.; Stott, David J.; Thalamuthu, Anbupalam; Trollor, Julian; Tzourio, Christophe; Grond, Jeroen van der; Vernooij, Meike W.; Witte, Veronica A.; Wright, Margaret J.; Yang, Qiong; Morris, Zoe; Siggurdsson, Siggi; Psaty, Bruce; Villringer, Arno; Schmidt, Helena; Haberg, Asta K.; Duijn, Cornelia M. van; Jukema, J. Wouter; Dichgans, Martin; Sacco, Ralph L.; Wright, Clinton B.; Kremen, William S.; Becker, Lewis C.; Thompson, Paul M.; Mosley, Thomas H.; Wardlaw, Joanna M.; Ikram, M. Arfan; Adams, Hieab H. H.; Seshadri, Sudha; Sachdev, Perminder S.; Smith, Stephen M.; Launer, Lenore; Longstreth, William; DeCarli, Charles; Schmidt, Reinhold; Fornage, Myriam; Debette, Stephanie und Nyquist, Paul A.
(2020):
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
In: Stroke, Bd. 51, Nr. 7: S. 2111-2121
[PDF, 1MB]