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PLoS genetics, 2012-07, Vol.8 (7), p.e1002824-e1002824
- Himes, Blanca E
- Jiang, Xiaofeng
- Hu, Ruoxi
- Wu, Ann C
- Lasky-Su, Jessica A
- Klanderman, Barbara J
- Ziniti, John
- Senter-Sylvia, Jody
- Lima, John J
- Irvin, Charles G
- Peters, Stephen P
- Meyers, Deborah A
- Bleecker, Eugene R
- Kubo, Michiaki
- Tamari, Mayumi
- Nakamura, Yusuke
- Szefler, Stanley J
- Lemanske, Jr, Robert F
- Zeiger, Robert S
- Strunk, Robert C
- Martinez, Fernando D
- Hanrahan, John P
- Koppelman, Gerard H
- Postma, Dirkje S
- Nieuwenhuis, Maartje A E
- Vonk, Judith M
- Panettieri, Jr, Reynold A
- Markezich, Amy
- Israel, Elliot
- Carey, Vincent J
- Tantisira, Kelan G
- Litonjua, Augusto A
- Lu, Quan
- Weiss, Scott T
- Ober, Carole
2012
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Epigenetics, 2013-12, Vol.8 (12), p.1254-1260
2013
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BMC systems biology, 2011-09, Vol.5 (147), p.153-153, Article 153
2011
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PLoS genetics, 2016-12, Vol.12 (12), p.e1006501-e1006501
2016
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PLoS genetics, 2019-12, Vol.15 (12), p.e1008500
- Kowalski, Madeline H
- Qian, Huijun
- Hou, Ziyi
- Rosen, Jonathan D
- Tapia, Amanda L
- Shan, Yue
- Jain, Deepti
- Argos, Maria
- Arnett, Donna K
- Avery, Christy
- Barnes, Kathleen C
- Becker, Lewis C
- Bien, Stephanie A
- Bis, Joshua C
- Blangero, John
- Boerwinkle, Eric
- Bowden, Donald W
- Buyske, Steve
- Cai, Jianwen
- Cho, Michael H
- Choi, Seung Hoan
- Choquet, Hélène
- Cupples, L Adrienne
- Cushman, Mary
- Daya, Michelle
- de Vries, Paul S
- Ellinor, Patrick T
- Faraday, Nauder
- Fornage, Myriam
- Gabriel, Stacey
- Ganesh, Santhi K
- Graff, Misa
- Gupta, Namrata
- He, Jiang
- Heckbert, Susan R
- Hidalgo, Bertha
- Hodonsky, Chani J
- Irvin, Marguerite R
- Johnson, Andrew D
- Jorgenson, Eric
- Kaplan, Robert
- Kardia, Sharon L R
- Kelly, Tanika N
- Kooperberg, Charles
- Lasky-Su, Jessica A
- Loos, Ruth J F
- Lubitz, Steven A
- Mathias, Rasika A
- McHugh, Caitlin P
- Montgomery, Courtney
- Moon, Jee-Young
- Morrison, Alanna C
- Palmer, Nicholette D
- Pankratz, Nathan
- Papanicolaou, George J
- Peralta, Juan M
- Peyser, Patricia A
- Rich, Stephen S
- Rotter, Jerome I
- Silverman, Edwin K
- Smith, Jennifer A
- Smith, Nicholas L
- Taylor, Kent D
- Thornton, Timothy A
- Tiwari, Hemant K
- Tracy, Russell P
- Wang, Tao
- Weiss, Scott T
- Weng, Lu-Chen
- Wiggins, Kerri L
- Wilson, James G
- Yanek, Lisa R
- Zöllner, Sebastian
- North, Kari E
- Auer, Paul L
- Raffield, Laura M
- Reiner, Alexander P
- Li, Yun
- Barsh, Gregory S.
2019
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EMBO reports, 2003-10, Vol.4 (10), p.1000-1004
2003
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PLoS genetics, 2011-08, Vol.7 (8), p.e1002216-e1002216
2011
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PLoS genetics, 2012-05, Vol.8 (5), p.e1002695
- Fox, Caroline S
- Liu, Yongmei
- White, Charles C
- Feitosa, Mary
- Smith, Albert V
- Heard-Costa, Nancy
- Lohman, Kurt
- Johnson, Andrew D
- Foster, Meredith C
- Greenawalt, Danielle M
- Griffin, Paula
- Ding, Jinghong
- Newman, Anne B
- Tylavsky, Fran
- Miljkovic, Iva
- Kritchevsky, Stephen B
- Launer, Lenore
- Garcia, Melissa
- Eiriksdottir, Gudny
- Carr, J Jeffrey
- Gudnason, Vilmunder
- Harris, Tamara B
- Cupples, L Adrienne
- Borecki, Ingrid B
- Bray, Molly
2012
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PLoS genetics, 2009-03, Vol.5 (3), p.e1000421-e1000421
2009
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PLoS genetics, 2019-02, Vol.15 (2), p.e1007949-e1007949
2019
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PloS one, 2014-03, Vol.9 (3), p.e92965-e92965
2014
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Molecular neurodegeneration, 2016-01, Vol.11 (7), p.7-7, Article 7
2016
Link zum Volltext
PLoS genetics, 2015-08, Vol.11 (8), p.e1005352-e1005352
- Iyengar, Sudha K
- Sedor, John R
- Freedman, Barry I
- Kao, W H Linda
- Kretzler, Matthias
- Keller, Benjamin J
- Abboud, Hanna E
- Adler, Sharon G
- Best, Lyle G
- Bowden, Donald W
- Burlock, Allison
- Chen, Yii-Der Ida
- Cole, Shelley A
- Comeau, Mary E
- Curtis, Jeffrey M
- Divers, Jasmin
- Drechsler, Christiane
- Duggirala, Ravi
- Elston, Robert C
- Guo, Xiuqing
- Huang, Huateng
- Hoffmann, Michael Marcus
- Howard, Barbara V
- Ipp, Eli
- Kimmel, Paul L
- Klag, Michael J
- Knowler, William C
- Kohn, Orly F
- Leak, Tennille S
- Leehey, David J
- Li, Man
- Malhotra, Alka
- März, Winfried
- Nair, Viji
- Nelson, Robert G
- Nicholas, Susanne B
- O'Brien, Stephen J
- Pahl, Madeleine V
- Parekh, Rulan S
- Pezzolesi, Marcus G
- Rasooly, Rebekah S
- Rotimi, Charles N
- Rotter, Jerome I
- Schelling, Jeffrey R
- Seldin, Michael F
- Shah, Vallabh O
- Smiles, Adam M
- Smith, Michael W
- Taylor, Kent D
- Thameem, Farook
- Thornley-Brown, Denyse P
- Truitt, Barbara J
- Wanner, Christoph
- Weil, E Jennifer
- Winkler, Cheryl A
- Zager, Philip G
- Igo, Jr, Robert P
- Hanson, Robert L
- Langefeld, Carl D
- Williams, Scott M.
2015
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Journal of molecular and cellular cardiology, 2016-03, Vol.92, p.30-40
2016
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Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles
2007
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Nature reviews. Genetics, 2004-08, Vol.5 (8), p.598-609
2004
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The EMBO journal, 2002-10, Vol.21 (19), p.5079-5087
2002
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PLoS pathogens, 2007-09, Vol.3 (9), p.1250-1261
2007
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Journal of anatomy, 2006-10, Vol.209 (4), p.495-502
2006
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Journal of investigative dermatology, 2005-11, Vol.125 (5), p.1053-1062
2005
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Nature immunology, 2003-01, Vol.4 (1), p.44-8
2003
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The EMBO journal, 1997-08, Vol.16 (15), p.4606-4616
1997
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Molecular biology and evolution, 2022-01, Vol.39 (1)
2022
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PLoS pathogens, 2012-05, Vol.8 (5), p.e1002712-e1002712
2012
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Molecular brain, 2019-02, Vol.12 (1), p.15-15, Article 15
2019
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