Sean Joseph Jurgens (Sean J Jurgens)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 33

Top Topics

Oral Anticoagulants

Aortic Aneurysm

Genome Wide Association Study

Top Venues

Nature communications

Nature genetics

medRxiv : the preprint server for health sciences

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

Publications

Justine Ryu, Joel T Rämö, Sean Joseph Jurgens, Teemu J Niiranen, Simone Sanna-Cherchi, Kenneth A Bauer, Amelia K Haj, Seung Hoan Choi, Aarno Palotie, Mark Daly, Patrick T Ellinor, Pavan K Bendapudi
Thrombosis Risk in Double Heterozygous Carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank. Blood (2024)
Joel T Rämö, Bryan Gorman, Lu-Chen Weng, Sean Joseph Jurgens, Panisa Singhanetr, Marisa G Tieger, Elon Hc van Dijk, Christopher W Halladay, Xin Wang, Joost Brinks, Seung Hoan Choi, Yuyang Luo, null null, null null, Saiju Pyarajan, Cari L Nealon, Michael B Gorin, Wen-Chih Wu, Lucia Sobrin, Kai Kaarniranta, Suzanne Yzer, Aarno Palotie, Neal S Peachey, Joni A Turunen, Camiel Jf Boon, Patrick T Ellinor, Sudha K Iyengar, Mark J Daly, Elizabeth J Rossin
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma. medRxiv : the preprint server for health sciences (2024)
Joel T Rämö, Bryan Gorman, Lu-Chen Weng, Sean Joseph Jurgens, Panisa Singhanetr, Marisa G Tieger, Elon Hc van Dijk, Christopher W Halladay, Xin Wang, Joost Brinks, Seung Hoan Choi, Yuyang Luo, null null, Saiju Pyarajan, Cari L Nealon, Michael B Gorin, Wen-Chih Wu, Lucia Sobrin, Kai Kaarniranta, Suzanne Yzer, Aarno Palotie, Neal S Peachey, Joni A Turunen, Camiel Jf Boon, Patrick T Ellinor, Sudha K Iyengar, Mark J Daly, Elizabeth J Rossin
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma. medRxiv : the preprint server for health sciences (2024)
Joel T Rämö, Bryan Gorman, Lu-Chen Weng, Sean Joseph Jurgens, Panisa Singhanetr, Marisa G Tieger, Elon Hc van Dijk, Christopher W Halladay, Xin Wang, Joost Brinks, Seung Hoan Choi, Yuyang Luo, null null, Saiju Pyarajan, Cari L Nealon, Michael B Gorin, Wen-Chih Wu, Lucia Sobrin, Kai Kaarniranta, Suzanne Yzer, Aarno Palotie, Neal S Peachey, Joni A Turunen, Camiel Jf Boon, Patrick T Ellinor, Sudha K Iyengar, Mark J Daly, Elizabeth J Rossin
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma. medRxiv : the preprint server for health sciences (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Justine Ryu, Joel T Rämö, Sean Joseph Jurgens, Teemu J Niiranen, Simone Sanna-Cherchi, Kenneth A Bauer, Amelia K Haj, Seung Hoan Choi, Aarno Palotie, Mark Daly, Patrick T Ellinor, Pavan K Bendapudi
Thrombosis Risk in Double Heterozygous Carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank. Blood (2024)
James Paul Pirruccello, Paolo Di Achille, Seung Hoan Choi, Joel T Rämö, Shaan Khurshid, Mahan Nekoui, Sean Joseph Jurgens, Victor Nauffal, Shinwan Kany, null null, Kenney Ng, Samuel Freesun Friedman, Puneet Batra, Kathryn L Lunetta, Aarno Palotie, Anthony A Philippakis, Jennifer E Ho, Steven A Lubitz, Patrick T Ellinor
Deep learning of left atrial structure and function provides link to atrial fibrillation risk. Nature communications 15 (1) (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Joel T Rämö, Bryan Gorman, Lu-Chen Weng, Sean Joseph Jurgens, Panisa Singhanetr, Marisa G Tieger, Elon Hc van Dijk, Christopher W Halladay, Xin Wang, Joost Brinks, Seung Hoan Choi, Yuyang Luo, null null, null null, Saiju Pyarajan, Cari L Nealon, Michael B Gorin, Wen-Chih Wu, Lucia Sobrin, Kai Kaarniranta, Suzanne Yzer, Aarno Palotie, Neal S Peachey, Joni A Turunen, Camiel Jf Boon, Patrick T Ellinor, Sudha K Iyengar, Mark J Daly, Elizabeth J Rossin
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma. medRxiv : the preprint server for health sciences (2024)
Joel T Rämö, Sean Joseph Jurgens, Shinwan Kany, Seung Hoan Choi, Xin Wang, Andrey N Smirnov, Samuel Freesun Friedman, Mahnaz Maddah, Shaan Khurshid, Patrick T Ellinor, James Paul Pirruccello
Rare Genetic Variants in LDLR , APOB , and PCSK9 are Associated with Aortic Stenosis. Circulation (2024)
James Paul Pirruccello, Paolo Di Achille, Seung Hoan Choi, Joel T Rämö, Shaan Khurshid, Mahan Nekoui, Sean Joseph Jurgens, Victor Nauffal, Shinwan Kany, null null, Kenney Ng, Samuel Freesun Friedman, Puneet Batra, Kathryn L Lunetta, Aarno Palotie, Anthony A Philippakis, Jennifer E Ho, Steven A Lubitz, Patrick T Ellinor
Deep learning of left atrial structure and function provides link to atrial fibrillation risk. Nature communications 15 (1) (2024)
Justine Ryu, Joel T Rämö, Sean Joseph Jurgens, Teemu J Niiranen, Simone Sanna-Cherchi, Kenneth A Bauer, Amelia K Haj, Seung Hoan Choi, Aarno Palotie, Mark Daly, Patrick T Ellinor, Pavan K Bendapudi
Thrombosis Risk in Double Heterozygous Carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank. Blood (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
James Paul Pirruccello, Paolo Di Achille, Seung Hoan Choi, Joel T Rämö, Shaan Khurshid, Mahan Nekoui, Sean Joseph Jurgens, Victor Nauffal, Shinwan Kany, null null, Kenney Ng, Samuel Freesun Friedman, Puneet Batra, Kathryn L Lunetta, Aarno Palotie, Anthony A Philippakis, Jennifer E Ho, Steven A Lubitz, Patrick T Ellinor
Deep learning of left atrial structure and function provides link to atrial fibrillation risk. Nature communications 15 (1) (2024)
Sean Joseph Jurgens, Xin Wang, Seung Hoan Choi, Lu-Chen Wang, Satoshi Koyama, James Paul Pirruccello, Trang T Nguyen, Patrick Smadbeck, Dongkeun Jang, Mark D Chaffin, Roddy Walsh, Carolina Roselli, Amanda L Elliott, Leonoor F J M Wijdeveld, Kiran J Biddinger, Shinwan Kany, Joel T Rämö, Pradeep Natarajan, Krishna G Aragam, Jason Flannick, Noël P Burtt, Connie R Bezzina, Steven A Lubitz, Kathryn L Lunetta, Patrick T Ellinor
Rare coding variant analysis for human diseases across biobanks and ancestries. Nature genetics (2024)
Justine Ryu, Joel T Rämö, Sean Joseph Jurgens, Teemu J Niiranen, Simone Sanna-Cherchi, Kenneth A Bauer, Amelia K Haj, Seung Hoan Choi, Aarno Palotie, Mark Daly, Patrick T Ellinor, Pavan K Bendapudi
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank. Blood 143 (23) (2024)
James Paul Pirruccello, Paolo Di Achille, Seung Hoan Choi, Joel T Rämö, Shaan Khurshid, Mahan Nekoui, Sean Joseph Jurgens, Victor Nauffal, Shinwan Kany, null null, Kenney Ng, Samuel Freesun Friedman, Puneet Batra, Kathryn L Lunetta, Aarno Palotie, Anthony A Philippakis, Jennifer E Ho, Steven A Lubitz, Patrick T Ellinor
Deep learning of left atrial structure and function provides link to atrial fibrillation risk. Nature communications 15 (1) (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Justine Ryu, Joel T Rämö, Sean Joseph Jurgens, Teemu J Niiranen, Simone Sanna-Cherchi, Kenneth A Bauer, Amelia K Haj, Seung Hoan Choi, Aarno Palotie, Mark Daly, Patrick T Ellinor, Pavan K Bendapudi
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank. Blood 143 (23) (2024)
Erik Schoenmakers, Federica Marelli, Helle F Jørgensen, W. Edward Visser, Carla Moran, Stefan Groeneweg, Carolina Avalos, Sean Joseph Jurgens, Nichola Figg, Alison Finigan, Neha Wali, Maura Agostini, Hannah Wardle-Jones, Greta Lyons, Rosemary Rusk, Deepa Gopalan, Philip Twiss, Jacob J Visser, Martin Goddard, Samer A M Nashef, Robin Heijmen, Paul Clift, Sanjay Sinha, James Paul Pirruccello, Patrick T Ellinor, Elisabeth M Busch-Nentwich, Ramiro Ramirez-Solis, Michael P Murphy, Luca Persani, Martin R Bennett, Krishna Chatterjee
Selenoprotein deficiency disorder predisposes to aortic aneurysm formation. Nature communications 14 (1) (2023)
Lara Curran, Antonio de Marvao, Paolo Inglese, Kathryn Anne McGurk, Pierre-Raphaël Schiratti, Adam Clement, Sean L Zheng, Surui Li, Chee Jian Pua, Mit Shah, Mina Jafari, Pantazis I Theotokis, Rachel J Buchan, Sean Joseph Jurgens, Claire E Raphael, Arun John Baksi, Antonis Pantazis, Brian P Halliday, Dudley John Pennell, Wenjia Bai, Calvin Woon-Loong Chin, Rafik Tadros, Connie R Bezzina, Hugh C Watkins, Stuart Alexander Cook, Sanjay K Prasad, James Simon Ware, Declan P O'Regan
Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine (2023)
Alex Lipov, Sean Joseph Jurgens, Francesco Mazzarotto, Mona Allouba, James Paul Pirruccello, Yasmine Aguib, Massimo Gennarelli, Magdi H Yacoub, Patrick T Ellinor, Connie R Bezzina, Roddy Walsh
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies. Nature cardiovascular research 2 (11) (2023)
Alex Lipov, Sean Joseph Jurgens, Francesco Mazzarotto, Mona Allouba, James Paul Pirruccello, Yasmine Aguib, Massimo Gennarelli, Magdi H Yacoub, Patrick T Ellinor, Connie R Bezzina, Roddy Walsh
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies. Nature cardiovascular research 2 (11) (2023)
Sean Joseph Jurgens, James P Pirruccello, Seung Hoan Choi, Valerie N Morrill, Mark D Chaffin, Steven A Lubitz, Kathryn L Lunetta, Patrick T Ellinor
Adjusting for common variant polygenic scores improves yield in rare variant association analyses. Nature genetics (2023)
Caroline Pham, Karolina Andrzejczyk, Sean Joseph Jurgens, Ronald H Lekanne Deprez, Kaylin C A Palm, Alexa M C Vermeer, Janneke Nijman, Imke Christiaans, Pascal F H M van Dessel, Leander Beekman, Seung Hoan Choi, Steven A Lubitz, Doris Skoric-Milosavljevic, Lisa M van den Bersselaar, Philip R Jansen, Jaël S Copier, Patrick T Ellinor, Arthur A M Wilde, Connie R Bezzina, Elisabeth M Lodder
Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias. Circulation. Genomic and precision medicine (2023)
Stephanie M Van der Voorn, Esmée van Drie, Virginnio Proost, Kristina Dimitrova, null Netherlands Acm/Pln Registry, Robert F Ernst, Cynthia A James, Crystal Tichnell, Brittney Murray, Hugh Calkins, Ardan Muammer Saguner, Firat Duru, Patrick T Ellinor, Connie R Bezzina, Sean Joseph Jurgens, J Peter van Tintelen, Toon A B van Veen
Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies. International journal of molecular sciences 24 (21) (2023)
Victor Nauffal, Valerie N Morrill, Sean Joseph Jurgens, Seung Hoan Choi, Amelia W Hall, Lu-Chen Weng, Jennifer L Halford, Christina A Austin-Tse, Christopher M Haggerty, Stephanie L Harris, Eugene K Wong, Alvaro Alonso, Dan E Arking, Emelia J Benjamin, Eric Boerwinkle, Yuan-I Min, Adolfo Correa, Brandon K Fornwalt, Susan R Heckbert, null null, Charles Kooperberg, Henry J Lin, Ruth J F Loos, Kenneth M Rice, Namrata Gupta, Thomas W Blackwell, Braxton D Mitchell, Alanna C Morrison, Bruce M Psaty, Wendy S Post, Susan Redline, Michael J Bamshad, Stephen S Rich, Jerome I Rotter, Elsayed Z Soliman, Nona Sotoodehnia, Kathryn L Lunetta, Patrick T Ellinor, Steven A Lubitz, null null
Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation 145 (20) (2022)
Saaket Agrawal, Minxian Wang, Marcus D R Klarqvist, Kirk Smith, Joseph Shin, Hesam Dashti, Nathaniel Diamant, Seung Hoan Choi, Sean Joseph Jurgens, Patrick T Ellinor, Anthony Philippakis, Melina Claussnitzer, Kenney Ng, Miriam S Udler, Puneet Batra, Amit V Khera
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Nature communications 13 (1) (2022)
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Floriane Simonet, Sean Joseph Jurgens, Manon Baudic, Michele Nicastro, Franck Potet, Joost A Offerhaus, Roddy Walsh, Seung Hoan Choi, Arjan C Houweling, Yuka Mizusawa, Soraya Anys, Damien Minois, Marine Arnaud, Josselin Duchateau, Yanushi D Wijeyeratne, Alison Muir, Michael Papadakis, Silvia Castelletti, Margherita Torchio, Cristina Gil Ortuño, Javier Lacunza, Daniela Francesca Giachino, Natascia Cerrato, Raphaël P Martins, Òscar Campuzano, Sonia Van Dooren, Aurélie Thollet, Florence Kyndt, Andrea Mazzanti, Nicolas Clémenty, Arnaud Bisson, Anniek Corveleyn, Birgit Stallmeyer, Sven Dittmann, Johan Saenen, Antoine Noël, Shohreh Honarbakhsh, Boris Rudic, Halim Marzak, Matthew K Rowe, Claire Federspiel, Sophie Le Page, Leslie Placide, Antoine Milhem, Hector Barajas-Martinez, Britt-Maria Beckmann, Ingrid P Krapels, Johannes Steinfurt, Bo Gregers Winkel, Reza Jabbari, Moore B Shoemaker, Bas J Boukens, Doris Škorić-Milosavljević, Hennie Bikker, Federico Manevy, Peter Lichtner, Marta Ribasés, Thomas Meitinger, Martina Müller-Nuraysid, null null, Jan Herman Veldink, Leonard H van den Berg, Philip Van Damme, Daniele Cusi, Chiara Lanzani, Sidwell Rigade, Eric Charpentier, Estelle Baron, Stéphanie Bonnaud, Simon Lecointe, Audrey Donnart, Hervé Le Marec, Stéphanie Chatel, Matilde Karakachoff, Stephane Bezieau, Barry London, Jacob Tfelt-Hansen, Dan Roden, Katja E Odening, Marina Cerrone, Larry A Chinitz, Paul G Volders, Maarten P van den Berg, Gabriel Laurent, Laurence Faivre, Charles Antzelevitch, Stefan Kääb, Alain Al Arnaout, Jean-Marc Dupuis, Jean-Luc Pasquie, Olivier Billon, Jason D Roberts, Laurence Jesel, Martin Borggrefe, Pier D Lambiase, Jacques Mansourati, Bart Loeys, Antoine Leenhardt, Pascale Guicheney, Philippe Maury, Eric Schulze-Bahr, Tomas Robyns, Jeroen Breckpot, Dominique Babuty, Silvia G Priori, Carlo Napolitano, null null, Carlos De Asmundis, Pedro Brugada, Ramon Brugada, Elena Arbelo, Josep Brugada, Philippe Mabo, Nathalie Behar, Carla Giustetto, Maria Sabater Molina, Juan R Gimeno, Can Hasdemir, Peter J Schwartz, Lia Crotti, Pascal P McKeown, Sanjay Sharma, Elijah R Behr, Michel Haissaguerre, Frédéric Sacher, Caroline Rooryck, Hanno L Tan, Carol A Remme, Pieter G Postema, Mario Delmar, Patrick T Ellinor, Steven A Lubitz, Jean-Baptiste Gourraud, Michael W T Tanck, Alfred L George, Calum A MacRae, Maged M Costantine, Christian Dina, Vincent Probst, Arthur A Wilde, Jean-Jacques Schott, Richard Redon, Connie R Bezzina
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature genetics 54 (3) (2022)
James Paul Pirruccello, Paolo Di Achille, Victor Nauffal, Mahan Nekoui, Samuel F Friedman, Marcus D R Klarqvist, Mark D Chaffin, Lu-Chen Wang, Jonathan W Cunningham, Shaan Khurshid, Carolina Roselli, Honghuang Lin, Satoshi Koyama, Shefali S Verma, Yoichiro Kamatani, Issei Komuro, null null, Sean Joseph Jurgens, Emelia J Benjamin, Puneet Batra, Pradeep Natarajan, Kenney Ng, Udo Hoffmann, Steven A Lubitz, Jennifer E Ho, Mark E Lindsay, Anthony A Philippakis, Patrick T Ellinor
Genetic analysis of right heart structure and function in 40,000 people. Nature genetics 54 (6) (2022)
Jennifer L Halford, Valerie N Morrill, Seung Hoan Choi, Sean Joseph Jurgens, Giorgio Melloni, Nicholas A Marston, Lu-Chen Wang, Victor Nauffal, Amelia W Hall, Sophia Gunn, Christina A Austin-Tse, James Paul Pirruccello, Shaan Khurshid, Heidi L Rehm, Emelia J Benjamin, Eric Boerwinkle, Jennifer A Brody, Adolfo Correa, Brandon K Fornwalt, Namrata Gupta, Christopher M Haggerty, Stephanie Harris, Susan R Heckbert, Charles C Hong, Charles Kooperberg, Henry J Lin, Ruth J F Loos, Braxton D Mitchell, Alanna C Morrison, Wendy Post, Bruce M Psaty, Susan Redline, Kenneth M Rice, Stephen S Rich, Jerome I Rotter, Peter F Schnatz, Elsayed Z Soliman, Nona Sotoodehnia, Eugene K Wong, null null, Marc S Sabatine, Christian T Ruff, Kathryn L Lunetta, Patrick T Ellinor, Steven A Lubitz
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature communications 13 (1) (2022)
Jennifer L Halford, Valerie N Morrill, Seung Hoan Choi, Sean Joseph Jurgens, Giorgio Melloni, Nicholas A Marston, Lu-Chen Wang, Victor Nauffal, Amelia W Hall, Sophia Gunn, Christina A Austin-Tse, James Paul Pirruccello, Shaan Khurshid, Heidi L Rehm, Emelia J Benjamin, Eric Boerwinkle, Jennifer A Brody, Adolfo Correa, Brandon K Fornwalt, Namrata Gupta, Christopher M Haggerty, Stephanie Harris, Susan R Heckbert, Charles C Hong, Charles Kooperberg, Henry J Lin, Ruth J F Loos, Braxton D Mitchell, Alanna C Morrison, Wendy Post, Bruce M Psaty, Susan Redline, Kenneth M Rice, Stephen S Rich, Jerome I Rotter, Peter F Schnatz, Elsayed Z Soliman, Nona Sotoodehnia, Eugene K Wong, null null, Marc S Sabatine, Christian T Ruff, Kathryn L Lunetta, Patrick T Ellinor, Steven A Lubitz
Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature communications 13 (1) (2022)
Sean Joseph Jurgens, Seung Hoan Choi, Valerie N Morrill, Mark D Chaffin, James Paul Pirruccello, Jennifer L Halford, Lu-Chen Wang, Victor Nauffal, Carolina Roselli, Amelia W Hall, Matthew T Oetjens, Braxton Lagerman, David P vanMaanen, null null, Krishna G Aragam, Kathryn L Lunetta, Christopher M Haggerty, Steven A Lubitz, Patrick T Ellinor
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. Nature genetics 54 (3) (2022)