Xin Wang

ORCID

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 7

Top Venues

medRxiv : the preprint server for health sciences

Nature genetics

Journal of human genetics

Circulation

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

Publications

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)
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)
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)
Xin Wang, Justine Ryu, Jihoon Kim, Andrea Ramirez, Kelsey R Mayo, null null, Henry Condon, Nataraja Sarma Vaitinadin, Lucila Ohno-Machado, Greg A Talavera, Patrick T Ellinor, Steven A Lubitz, Seung Hoan Choi
Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program. Journal of human genetics (2023)

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Publication Activity (10 Years)

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Xin Wang