Martina Brueckner

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 12

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Nature genetics

Nature reviews. Cardiology

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

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, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
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, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
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, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
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, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
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, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Sencicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 120 (16) (2023)
Syndi Barish, Kathryn Berg, Jeffrey Drozd, Isabella Berglund-Brown, Labeeqa Khizir, Lauren K Wasson, Christine E Seidman, Jonathan G Seidman, Sidi Chen, Martina Brueckner
The H2Bub1-deposition complex is required for human and mouse cardiogenesis. Development (Cambridge, England) 150 (23) (2023)
Lydia Djenoune, Kathryn Berg, Martina Brueckner, Shiaulou Yuan
A change of heart: new roles for cilia in cardiac development and disease. Nature reviews. Cardiology (2021)
Weizhen Ji, Dina Ferdman, Joshua Copel, Dustin Scheinost, Veronika Shabanova, Martina Brueckner, Mustafa K Khokha, Laura R Ment
De novo damaging variants associated with congenital heart diseases contribute to the connectome. Scientific reports 10 (1) (2020)
Felix Richter, Sarah U Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K Wasson, Kathleen M Chen, Jian Zhou, Hongjian Qi, Nihir Patel, Steven R DePalma, Michael Parfenov, Jason Homsy, Joshua M Gorham, Kathryn B Manheimer, Matthew Velinder, Andrew Farrell, Gabor T Marth, Eric E Schadt, Jonathan R Kaltman, Jane W Newburger, Alessandro Giardini, Elizabeth Goldmuntz, Martina Brueckner, Richard Kim, George A Porter, Daniel Bernstein, Wendy K Chung, Deepak Srivastava, Martin Tristani-Firouzi, Olga G Troyanskaya, Diane E Dickel, Yufeng Shen, Jonathan G Seidman, Christine E Seidman, Bruce D Gelb
Genomic analyses implicate noncoding de novo variants in congenital heart disease. Nature genetics 52 (8) (2020)
Andrew Robson, Svetlana Z Makova, Syndi Barish, Samir Zaidi, Sameet Mehta, Jeffrey Drozd, Sheng Chih Jin, Bruce D Gelb, Christine E Seidman, Wendy K Chung, Richard P Lifton, Mustafa K Khokha, Martina Brueckner
Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility. Proceedings of the National Academy of Sciences of the United States of America 116 (28) (2019)
W Scott Watkins, E Javier Hernandez, Sergiusz Wesołowski, Brent W Bisgrove, Ryan T Sunderland, Edwin Lin, Gordon Lemmon, Bradley L Demarest, Thomas A Miller, Daniel Bernstein, Martina Brueckner, Wendy K Chung, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Christine E Seidman, Yufeng Shen, H Joseph Yostl, Mark Yandell, Martin Tristani-Firouzi
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes. Nature communications 10 (1) (2019)
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant, Wei-Chien Hung, Shozeb M Haider, Junhui Zhang, James R Knight, Robert D Bjornson, Christopher Castaldi, Irina R Tikhonoa, Kaya Bilguvar, Shrikant M Mane, Stephan J Sanders, Seema Mital, Mark W Russell, J William Gaynor, John Deanfield, Alessandro Giardini, George A Porter, Deepak Srivastava, Cecelia W Lo, Yufeng Shen, W Scott Watkins, Mark Yandell, H Joseph Yost, Martin Tristani-Firouzi, Jane W Newburger, Amy E Roberts, Richard Kim, Hongyu Zhao, Jonathan R Kaltman, Elizabeth Goldmuntz, Wendy K Chung, Jonathan G Seidman, Bruce D Gelb, Christine E Seidman, Richard P Lifton, Martina Brueckner
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. Nature genetics 49 (11) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Martina Brueckner