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Martina Brueckner obtained her BS and MD degrees from the University of Virginia, followed by a Pediatric Residency at the University of Pittsburgh and a Pediatric Cardiology Fellowship at Yale University School of Medicine. Her clinical and research focus is genetics of congenital heart disease (CHD). The goal of the lab's work is to determine the genetic cause and developmental mechanisms underlying CHD with a focus on the function of cilia in heart development. Our work aims to bridge research in the basic developmental biology mechanisms underlying development of the embryonic left-right axis with clinical pediatric cardiology and cardiac genetics. The laboratory has been integral in understanding the cellular and molecular mechanism underlying vertebrate LR asymmetry, identifying genes and mechanism by which motile and immotile cilia establish an early asymmetric calcium signal that is essential to normal LR development of the heart. As part of the Pediatric Cardiac Genomics Consortium (PCGC), we are now combining our understanding of the basic biology underlying left-right development with state-of-the-art genomic approaches to a more comprehensive understanding of human CHD. We are focusing on the ability to identify the genetic causes of CHD, and to directly test putative genetic causes of human CHD identified from genomic analysis of patient DNA in animal model systems including mouse and zebrafish, and finally to link genetic and developmental mechanisms of CHD to improved care of patients with CHD.
Dr. Brueckner's clinical focus is on patients with genetic causes of congenital heart disease. It has become increasingly apparent that a large portion of cardiovascular disease in children and adolescents has as its underlying etiology a genetic defect. Dr. Brueckner co-founded one of the first pediatric cardiac genetics clinics at Yale-New Haven Children's Hospital. The clinic provides comprehensive diagnostic evaluation and follow-up care for patients with genetic-cardiovascular disease. Dr. Brueckner has been a staff cardiologist since completing her fellowship at Yale in 1990.
Dr. Brueckner's clinical focus is on patients with genetic causes of congenital heart disease. It has become increasingly apparent that a large portion of cardiovascular disease in children and adolescents has as its underlying etiology a genetic defect. Dr. Brueckner co-founded one of the first pediatric cardiac genetics clinics at Yale-New Haven Children's Hospital. The clinic provides comprehensive diagnostic evaluation and follow-up care for patients with genetic-cardiovascular disease. Dr. Brueckner has been a staff cardiologist since completing her fellowship at Yale in 1990.
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论文共 92 篇作者统计合作学者相似作者
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Lara Maleyeff,Jane W. Newburger,David Wypij,Nina H. Thomas, Evdokia Anagnoustou,Martina Brueckner,Wendy K. Chung,John Cleveland, Sean Cunningham,Bruce D. Gelb,Elizabeth Goldmuntz,Donald J. Hagler,
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGYno. 2 (2024): 278-290
Ketu Mishra-Gorur, Tanyeri Barak,Leon D. Kaulen,Octavian Henegariu,Sheng Chih Jin, Stephanie Marie Aguilera, Ezgi Yalbir, Gizem Goles,Sayoko Nishimura,Danielle Miyagishima,Lydia Djenoune, Selin Altinok,
W Scott Watkins, E Javier Hernandez, Thomas A Miller,Nathan R Blue, Raquel Zimmerman,Eric R Griffiths,Erwin Frise,Daniel Bernstein,Marko T Boskovski,Martina Brueckner,Wendy K Chung,J William Gaynor,
medRxiv : the preprint server for health sciences (2024)
Matthew P. O'Brien,Marina V. Pryzhkova,Evelyn M. R. Lake,Francesca Mandino,Xilin Shen,Ruchika Karnik, Alisa Atkins, Michelle J. Xu,Weizhen Ji,Monica Konstantino,Martina Brueckner,Laura R. Ment,
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESno. 1 (2024): 430
bioRxiv : the preprint server for biology (2024)
Circulation. Genomic and precision medicineno. 2 (2023): e003791-e003791
Circulation. Genomic and precision medicineno. 3 (2023): 224-231
Syndi Barish,Kathryn Berg, Jeffrey Drozd,Isabella Berglund-Brown,Labeeqa Khizir,Lauren K. Wasson,Christine E. Seidman, Jonathan G. Seidman,Sidi Chen,Martina Brueckner
DEVELOPMENTno. 23 (2023)
Richa Tambi, Binte Zehra, Sharon Nandkishore, Shermin Sharafat, Faiza Kader,Nasna Nassir,Nesrin Mohamed,Awab Ahmed,Reem Abdel Hameid, Samah Alasrawi,Martina Brueckner, Wolfgang M. Kuebler,
Physiological genomicsno. 12 (2023): 634-646
Matthew J Lewis,Alexander Hsieh,Lu Qiao,Renjie Tan,Brigitte Kazzi, Alexandra Channing,Emily L Griffin,Vaidehi Jobanputra,Jennifer Su,Chowdhury Shahryar,Lazaros Kochilas,J William Gaynor,
Circulation. Genomic and precision medicineno. 2 (2023): e003900-e003900
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