Muench, Johannes; Engesser, Marie; Schoenauer, Ria; Hamm, J. Austin; Hartig, Christin; Hantmann, Elena; Akay, Gulsen; Pehlivan, Davut; Mitani, Tadahiro; Akdemir, Zeynep Coban; Tuysuz, Beyhan; Shirakawa, Toshihiko; Dateki, Sumito; Claus, Laura R.; van Eerde, Albertien M.; Smol, Thomas; Devisme, Louise; Franquet, Helene; Attie-Bitach, Tania; Wagner, Timo; Bergmann, Carsten; Hoehn, Anne Kathrin; Shril, Shirlee; Pollack, Ari; Wenger, Tara; Scott, Abbey A.; Paolucci, Sarah; Buchan, Jillian; Gabriel, George C.; Posey, Jennifer E.; Lupski, James R.; Petit, Florence; McCarthy, Andrew A.; Pazour, Gregory J.; Lo, Cecilia W.; Popp, Bernt; Halbritter, Jan

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

CELL REPORTS MEDICINE

IF10.6

2022-02-014

OAAI

Teekakirikul, Polakit; Zhu, Wenjuan; Xu, Xinxiu; Young, Cullen B.; Tan, Tuantuan; Smith, Amanda M.; Wang, Chengdong; Peterson, Kevin A.; Gabriel, George C.; Ho, Sebastian; Sheng, Yi; de Bellaing, Anne Moreau; Sonnenberg, Daniel A.; Lin, Jiuann-huey; Fotiou, Elisavet; Tenin, Gennadiy; Wang, Michael X.; Wu, Yijen L.; Feinstein, Timothy; Devine, William; Gou, Honglan; Bais, Abha S.; Glennon, Benjamin J.; Zahid, Maliha; Wong, Timothy C.; Ahmad, Ferhaan; Rynkiewicz, Michael J.; Lehman, William J.; Keavney, Bernard; Alastalo, Tero-Pekka; Freckmann, Mary-Louise; Orwig, Kyle; Murray, Steve; Ware, Stephanie M.; Zhao, Hui; Feingold, Brian; Lo, Cecilia W.

Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strength

DEVELOPMENT

IF3.6

2021-10-046

OAAI

Cardiovascular Development and Congenital Heart Disease Modeling in the Pig

JOURNAL OF THE AMERICAN HEART ASSOCIATION

IF5.3

2021-07-2027

OAAI

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

HUMAN GENETICS AND GENOMICS ADVANCES

IF3.6

2021-07-0111

OAAI

Teekakirikul, Polakit; Zhu, Wenjuan; Gabriel, George C.; Young, Cullen B.; Williams, Kylia; Martin, Lisa J.; Hill, Jennifer C.; Richards, Tara; Billaud, Marie; Phillippi, Julie A.; Wang, Jianbin; Wu, Yijen; Tan, Tuantuan; Devine, William; Lin, Jiuann-huey; Bais, Abha S.; Klonowski, Jonathan; de Bellaing, Anne Moreau; Saini, Ankur; Wang, Michael X.; Emerel, Leonid; Salamacha, Nathan; Wyman, Samuel K.; Lee, Carrie; Li, Hung Sing; Miron, Anastasia; Zhang, Jingyu; Xing, Jianhua; McNamara, Dennis M.; Fung, Erik; Kirshbom, Paul; Mahle, William; Kochilas, Lazaros K.; He, Yihua; Garg, Vidu; White, Peter; McBride, Kim L.; Benson, D. Woodrow; Gleason, Thomas G.; Mital, Seema; Lo, Cecilia W.

Role of cilia in the pathogenesis of congenital heart disease

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

IF6

2021-02-0131

OAAI

Reply to 'Double-outlet right ventricle is not hypoplastic left heart syndrome'

NATURE GENETICS

IF31.8

2019-01-071

OAAI

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

GENOME BIOLOGY

IF9.4

2018-07-1740

OAAI

Prins, Bram P.; Mead, Timothy J.; Brody, Jennifer A.; Sveinbjornsson, Gardar; Ntalla, Ioanna; Bihlmeyer, Nathan A.; van den Berg, Marten; Bork-Jensen, Jette; Cappellani, Stefania; Van Duijvenboden, Stefan; Klena, Nikolai T.; Gabriel, George C.; Liu, Xiaoqin; Gulec, Cagri; Grarup, Niels; Haessler, Jeffrey; Hall, Leanne M.; Iorio, Annamaria; Isaacs, Aaron; Li-Gao, Ruifang; Lin, Honghuang; Liu, Ching-Ti; Lyytikainen, Leo-Pekka; Marten, Jonathan; Mei, Hao; Mueller-Nurasyid, Martina; Orini, Michele; Padmanabhan, Sandosh; Radmanesh, Farid; Ramirez, Julia; Robino, Antonietta; Schwartz, Molly; van Setten, Jessica; Smith, Albert V.; Verweij, Niek; Warren, Helen R.; Weiss, Stefan; Alonso, Alvaro; Arnar, David O.; Bots, Michiel L.; de Boer, Rudolf A.; Dominiczak, Anna F.; Eijgelsheim, Mark; Ellinor, Patrick T.; Guo, Xiuqing; Felix, Stephan B.; Harris, Tamara B.; Hayward, Caroline; Heckbert, Susan R.; Huang, Paul L.; Jukema, J. W.; Kahonen, Mika; Kors, Jan A.; Lambiase, Pier D.; Launer, Lenore J.; Li, Man; Linneberg, Allan; Nelson, Christopher P.; Pedersen, Oluf; Perez, Marco; Peters, Annette; Polasek, Ozren; Psaty, Bruce M.; Raitakari, Olli T.; Rice, Kenneth M.; Rotter, Jerome I.; Sinner, Moritz F.; Soliman, Elsayed Z.; Spector, Tim D.; Strauch, Konstantin; Thorsteinsdottir, Unnur; Tinker, Andrew; Trompet, Stella; Uitterlinden, Andre; Vaartjes, Ilonca; van der Meer, Peter; Voelker, Uwe; Voelzke, Henry; Waldenberger, Melanie; Wilson, James G.; Xie, Zhijun; Asselbergs, Folkert W.; Doerr, Marcus; van Duijn, Cornelia M.; Gasparini, Paolo; Gudbjartsson, Daniel F.; Gudnason, Vilmundur; Hansen, Torben; Kaeaeb, Stefan; Kanters, Jorgen K.; Kooperberg, Charles; Lehtimaki, Terho; Lin, Henry J.; Lubitz, Steven A.; Mook-Kanamori, Dennis O.; Conti, Francesco J.; Newton-Cheh, Christopher H.; Rosand, Jonathan; Rudan, Igor; Samani, Nilesh J.; Sinagra, Gianfranco; Smith, Blair H.; Holm, Hilma; Stricker, Bruno H.; Ulivi, Sheila; Sotoodehnia, Nona; Apte, Suneel S.; van der Harst, Pim; Stefansson, Kari; Munroe, Patricia B.; Arking, Dan E.; Lo, Cecilia W.; Jamshidi, Yalda

The complex genetics of hypoplastic left heart syndrome

NATURE GENETICS

IF31.8

2017-05-22161

OAAI

Liu, Xiaoqin; Yagi, Hisato; Saeed, Shazina; Bais, Abha S.; Gabriel, George C.; Chen, Zhaohan; Peterson, Kevin A.; Li, You; Schwartz, Molly C.; Reynolds, William T.; Saydmohammed, Manush; Gibbs, Brian; Wu, Yijen; Devine, William; Chatterjee, Bishwanath; Klena, Nikolai T.; Kostka, Dennis; Bentley, Karen L. de Mesy; Ganapathiraju, Madhavi K.; Dexheimer, Phillip; Leatherbury, Linda; Khalifa, Omar; Bhagat, Anchit; Zahid, Maliha; Pu, William; Watkins, Simon; Grossfeld, Paul; Murray, Stephen A.; Porter, George A., Jr.; Tsang, Michael; Martin, Lisa J.; Benson, D. Woodrow; Aronow, Bruce J.; Lo, Cecilia W.

Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography

JCI INSIGHT

IF6.1

2017-03-0935

MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates

NATURE GENETICS

IF31.8

2015-10-0562

OAAI

Guimier, Anne; Gabriel, George C.; Bajolle, Fanny; Tsang, Michael; Liu, Hui; Noll, Aaron; Schwartz, Molly; El Malti, Rajae; Smith, Laurie D.; Klena, Nikolai T.; Jimenez, Gina; Miller, Neil A.; Oufadem, Myriam; de Bellaing, Anne Moreau; Yagi, Hisato; Saunders, Carol J.; Baker, Candice N.; Di Filippo, Sylvie; Peterson, Kevin A.; Thiffault, Isabelle; Bole-Feysot, Christine; Cooley, Linda D.; Farrow, Emily G.; Masson, Cecile; Schoen, Patric; Deleuze, Jean-Francois; Nitschke, Patrick; Lyonnet, Stanislas; de Pontual, Loic; Murray, Stephen A.; Bonnet, Damien; Kingsmore, Stephen F.; Amiel, Jeanne; Bouvagnet, Patrice; Lo, Cecilia W.; Gordon, Christopher T.

Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families

NATURE GENETICS

IF31.8

2015-10-05133

OAAI

Akawi, Nadia; McRae, Jeremy; Ansari, Morad; Balasubramanian, Meena; Blyth, Moira; Brady, Angela F.; Clayton, Stephen; Cole, Trevor; Deshpande, Charu; Fitzgerald, Tomas W.; Foulds, Nicola; Francis, Richard; Gabriel, George; Gerety, Sebastian S.; Goodship, Judith; Hobson, Emma; Jones, Wendy D.; Joss, Shelagh; King, Daniel; Klena, Nikolai; Kumar, Ajith; Lees, Melissa; Lelliott, Chris; Lord, Jenny; McMullan, Dominic; O'Regan, Mary; Osio, Deborah; Piombo, Virginia; Prigmore, Elena; Rajan, Diana; Rosser, Elisabeth; Sifrim, Alejandro; Smith, Audrey; Swaminathan, Ganesh J.; Turnpenny, Peter; Whitworth, James; Wright, Caroline F.; Firth, Helen V.; Barrett, Jeffrey C.; Lo, Cecilia W.; FitzPatrick, David R.; Hurles, Matthew E.

Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies

HUMAN MOLECULAR GENETICS

IF3.2

2015-04-1545

OAAI

ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

NATURE COMMUNICATIONS

IF15.7

2015-01-2050

OAAI

George C. Gabriel

个人简介

教育背景

工作经历

荣誉奖项

研究方向