Slavé Petrovski

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 29

Top Topics

High Fat Diet Induced

Pulmonary Fibrosis

Top Venues

Nature genetics

Science advances

Nature communications

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

Publications

Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Lawrence Middleton, Ioannis Melas, Chirag Vasavda, Arwa Bin Raies, Benedek Rozemberczki, Ryan S Dhindsa, Justin S Dhindsa, Blake Weido, Quanli Wang, Andrew R Harper, Gavin Edwards, Slavé Petrovski, Dimitrios Michael Vitsios
Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Science advances 10 (19) (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Lawrence Middleton, Ioannis Melas, Chirag Vasavda, Arwa Bin Raies, Benedek Rozemberczki, Ryan S Dhindsa, Justin S Dhindsa, Blake Weido, Quanli Wang, Andrew R Harper, Gavin Edwards, Slavé Petrovski, Dimitrios Michael Vitsios
Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Science advances 10 (19) (2024)
Andrey Ziyatdinov, Jason M Torres, Jesus Alegre, Joshua D Backman, Joelle Mbatchou, Michael Turner, Sheila M Gaynor, Tyler Joseph, Yuxin Zou, Daren Liu, Rachel Wade, Jeffrey Staples, Razvan Panea, Alex Popov, Xiaodong Bai, Suganthi Balasubramanian, Lukas Habegger, Rouel Lanche, Alex Lopez, Evan Maxwell, Marcus Jones, Humberto Garcia-Ortiz, Raúl Ramírez-Reyes, Rogelio Santacruz-Benítez, Abhishek Nag, Katherine R Smith, Amy Damask, Nan Lin, Charles Paulding, Mark Reppell, Sebastian Zöllner, Eric Jorgensen, William Salerno, Slavé Petrovski, John Overton, Jeffrey G Reid, Timothy A Thornton, Gonçalo R Abecasis, Jaime Berumen-Campos, Lorena Orozco-Orozco, Rory Collins, null null, null null, Aris Baras, Michael R Hill, Jonathan R Emberson, Jonathan Marchini, Pablo Kuri-Morales, Roberto Tapia-Conyer
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Oliver S Burren, Ryan S Dhindsa, Sri V V Deevi, Sean Wen, Abhishek Nag, Jonathan Mitchell, Fengyuan Hu, Douglas P Loesch, Katherine R Smith, Neetu Razdan, Henric Olsson, Adam Platt, Dimitrios Michael Vitsios, Qiang Wu, null null, Veryan Codd, Christopher P Nelson, Nilesh J Samani, Ruth E March, Sebastian Wasilewski, Keren Jacqueline Carss, Margarete Fabre, Quanli Wang, Menelas N Pangalos, Slavé Petrovski
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences. Nature genetics (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Manik Garg, Marcin Karpinski, Dorota Matelska, Lawrence Middleton, Oliver S Burren, Fengyuan Hu, Eleanor Wheeler, Katherine R Smith, Margarete A Fabre, Jonathan Mitchell, Amanda O'Neill, Euan A Ashley, Andrew R Harper, Quanli Wang, Ryan S Dhindsa, Slavé Petrovski, Dimitrios Michael Vitsios
Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank. Nature genetics 56 (9) (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Lawrence Middleton, Ioannis Melas, Chirag Vasavda, Arwa Bin Raies, Benedek Rozemberczki, Ryan S Dhindsa, Justin S Dhindsa, Blake Weido, Quanli Wang, Andrew R Harper, Gavin Edwards, Slavé Petrovski, Dimitrios Michael Vitsios
Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Science advances 10 (19) (2024)
Yajie Zhao, Maria Chukanova, Katherine A Kentistou, Zammy Fairhurst-Hunter, Anna Maria Siegert, Raina Y Jia, Georgina K C Dowsett, Eugene J Gardner, Katherine L Lawler, Felix R Day, Lena R Kaisinger, Yi-Chun Loraine Tung, Brian Yee Hong Lam, Hsiao-Jou Cortina Chen, Quanli Wang, Jaime Berumen-Campos, Pablo Kuri-Morales, Roberto Tapia-Conyer, Jesus Alegre, Inês A Barroso, Jonathan R Emberson, Jason M Torres, Rory Collins, Danish Saleheen, Katherine R Smith, Dirk S Paul, Florian T Merkle, I Sadaf Farooqi, Nicholas J Wareham, Slavé Petrovski, Stephen I O'Rahilly, Ken K Ong, Giles S H Yeo, John R B Perry
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease. Nature genetics 56 (4) (2024)
Ryan S Dhindsa, Oliver S Burren, Benjamin B Sun, Bram P Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Andreas Bender, Ventzislava A Hristova, Katherine R Smith, Keren Jacqueline Carss, Sebastian Wasilewski, Andrew R Harper, Dirk S Paul, Margarete A Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, null null, Dimitrios Michael Vitsios, Euan A Ashley, Christopher D Whelan, Menelas N Pangalos, Quanli Wang, Slavé Petrovski
Rare variant associations with plasma protein levels in the UK Biobank. Nature (2023)
Yask Gupta, David J Friedman, Michelle T McNulty, Atlas Khan, Brandon M Lane, Chen Wang, Juntao Ke, Gina Jin, Benjamin Wooden, Andrea L Knob, Tze Y Lim, Gerald B Appel, Kinsie Huggins, Lili Liu, Adele Mitrotti, Megan C Stangl, Andrew Bomback, Nine V A M Knoers, Monica Bodria, Maddalena Marasà, Ning Shang, David J Cohen, Russell J Crew, William Morello, Pietro A Canetta, Jai Radhakrishnan, Jeremiah Martino, Qingxue Liu, Wendy K Chung, Angelica Espinoza, Yuan Luo, Wei-Qi Wei, QiPing Feng, Chunhua Weng, Yilu Fang, Iftikhar J Kullo, Mohammadreza Naderian, Nita Limdi, Marguerite R Irvin, Hemant Tiwari, Sumit Mohan, Maya Rao, Geoffrey K Dube, Ninad S Chaudhary, Orlando M Gutiérrez, Suzanne E Judd, Andrea N Edginton, Leslie A Lange, Ethan M Lange, Daniel L Bivona, Miguel Verbitsky, Cheryl A Winkler, Jeffrey B Kopp, Dominick Santoriello, Ibrahim Batal, Sérgio Veloso Brant Pinheiro, Eduardo Araújo Oliveira, Ana Cristina Dos Santos Lopes, Isabella Pisani, Enrico Fiaccadori, Fangming Lin, Loreto Gesualdo, Antonio Amoroso, Gian Marco Ghiggeri, Vivette D D'Agati, Riccardo Magistroni, Eimear E Kenny, Ruth J F Loos, Giovanni Montini, Friedhelm Hildebrandt, Dirk S Paul, Slavé Petrovski, David B Goldstein, Matthias Kretzler, Rasheed A Gbadegesin, Ali G Gharavi, Krzysztof Kiryluk, Matthew Gordon Sampson, Martin R Pollak, Simone Sanna-Cherchi
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Nature communications 14 (1) (2023)
Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver S Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria Jesus Martin, James David Stephenson, Kalpana Panneerselvam, Slavé Petrovski, Pablo Porras, Peter Nick Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael A Laffan, Willem Hendrik Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth A Bruford, Dragana Vuckovic
The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood (2023)
Benjamin B Sun, Joshua Chiou, Matthew Traylor, Christian Benner, Yi-Hsiang Hsu, Tom G Richardson, Praveen Surendran, Anubha Mahajan, Chloe Robins, Steven G Vasquez-Grinnell, Liping Hou, Erika M Kvikstad, Oliver S Burren, Jonathan Davitte, Kyle L Ferber, Christopher E Gillies, Åsa K Hedman, Sile Hu, Tinchi Lin, Rajesh Mikkilineni, Rion K Pendergrass, Corran Pickering, Bram Prins, Denis Baird, Chia-Yen Chen, Lucas D Ward, Aimee M Deaton, Samantha Welsh, Carissa M Willis, Nick Lehner, Matthias Arnold, Maria A Wörheide, Karsten Suhre, Gabi Kastenmüller, Anurag Sethi, Madeleine Cule, Anil Raj, null null, null null, null null, null null, null null, null null, null null, null null, null null, Lucy Burkitt-Gray, Eugene Melamud, Mary Helen Black, Eric B Fauman, Joanna M M Howson, Hyun Min Kang, Mark I McCarthy, Paul Nioi, Slavé Petrovski, Robert A Scott, Erin N Smith, Sandor Szalma, Dawn M Waterworth, Lyndon J Mitnaul, Joseph D Szustakowski, Bradford W Gibson, Melissa R Miller, Christopher D Whelan
Plasma proteomic associations with genetics and health in the UK Biobank. Nature (2023)
Andrey Ziyatdinov, Jason M Torres, Jesus Alegre, Joshua D Backman, Joelle Mbatchou, Michael Turner, Sheila M Gaynor, Tyler Joseph, Yuxin Zou, Daren Liu, Rachel Wade, Jeffrey Staples, Razvan Panea, Alex Popov, Xiaodong Bai, Suganthi Balasubramanian, Lukas Habegger, Rouel Lanche, Alex Lopez, Evan Maxwell, Marcus Jones, Humberto Garcia-Ortiz, Raúl Ramírez-Reyes, Rogelio Santacruz-Benítez, Abhishek Nag, Katherine R Smith, Amy Damask, Nan Lin, Charles Paulding, Mark Reppell, Sebastian Zöllner, Eric Jorgensen, William Salerno, Slavé Petrovski, John Overton, Jeffrey G Reid, Timothy A Thornton, Gonçalo R Abecasis, Jaime Berumen-Campos, Lorena Orozco-Orozco, Rory Collins, null null, null null, Aris Baras, Michael R Hill, Jonathan R Emberson, Jonathan Marchini, Pablo Kuri-Morales, Roberto Tapia-Conyer
Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature (2023)
Dimitrios Michael Vitsios, Ryan S Dhindsa, Dorota Matelska, Jonathan Mitchell, Xuequing Zou, Joshua Armenia, Fengyuan Hu, Quanli Wang, Ben S Sidders, Andrew R Harper, Slavé Petrovski
Cancer-driving mutations are enriched in genic regions intolerant to germline variation. Science advances 8 (34) (2022)
Abhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, Chirag Vasavda, Andrew R Harper, Dimitrios Michael Vitsios, Andrea Ahnmark, Bilada Bilican, Katja Madeyski-Bengtson, Bader Zarrouki, Anthony W Zoghbi, Quanli Wang, Katherine R Smith, Jesus Alegre, Pablo Kuri-Morales, Jaime Berumen-Campos, Roberto Tapia-Conyer, Jonathan R Emberson, Jason M Torres, Rory Collins, David M Smith, Benjamin G Challis, Dirk S Paul, Mohammad Bohlooly-Y, Mike Snowden, David Baker, Regina Fritsche Danielson, Menelas N Pangalos, Slavé Petrovski
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes. Science advances 8 (46) (2022)
Dimitrios Vitsios, Ryan S Dhindsa, Lawrence Middleton, Ayal B Gussow, Slavé Petrovski
Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning. Nature communications 12 (1) (2021)
Quanli Wang, Ryan S Dhindsa, Keren Carss, Andrew R Harper, Abhishek Nag, Ioanna Tachmazidou, Dimitrios Vitsios, Sri V V Deevi, Alex Mackay, Daniel Muthas, Michael Hühn, Susan Monkley, Henric Olsson, null null, Sebastian Wasilewski, Katherine R Smith, Ruth March, Adam Platt, Carolina Haefliger, Slavé Petrovski
Rare variant contribution to human disease in 281,104 UK Biobank exomes. Nature 597 (7877) (2021)
Gundula Povysil, Slavé Petrovski, Joseph Hostyk, Vimla Aggarwal, Andrew S Allen, David B Goldstein
Rare-variant collapsing analyses for complex traits: guidelines and applications. Nature reviews. Genetics 20 (12) (2019)
Sahar Gelfman, Quanli Wang, Yi-Fan Lu, Diana Hall, Christopher D Bostick, Ryan S Dhindsa, Matthew W Halvorsen, K Melodi McSweeney, Ellese Cotterill, Tom Edinburgh, Michael A Beaumont, Wayne N Frankel, Slavé Petrovski, Andrew S Allen, Michael J Boland, David B Goldstein, Stephen J Eglen
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays. PLoS computational biology 14 (10) (2018)
Slavé Petrovski, Jamie L Todd, Michael T Durheim, Quanli Wang, Jason W Chien, Fran L Kelly, Courtney Frankel, Caroline M Mebane, Zhong Ren, Joshua Bridgers, Thomas J Urban, Colin D Malone, Ashley Finlen Copeland, Christie Brinkley, Andrew S Allen, Thomas O'Riordan, John G McHutchison, Scott M Palmer, David B Goldstein
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis. American journal of respiratory and critical care medicine 196 (1) (2017)
Joshua Traynelis, Michael Silk, Quanli Wang, Samuel F Berkovic, Liping Liu, David B Ascher, David J Balding, Slavé Petrovski
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation. Genome research 27 (10) (2017)
Sahar Gelfman, Quanli Wang, K Melodi McSweeney, Zhong Ren, Francesca La Carpia, Matt Halvorsen, Kelly Schoch, Fanni Ratzon, Erin L Heinzen, Michael J Boland, Slavé Petrovski, David B Goldstein
Annotating pathogenic non-coding variants in genic regions. Nature communications 8 (1) (2017)
Ayal B Gussow, Brett R Copeland, Ryan S Dhindsa, Quanli Wang, Slavé Petrovski, William H Majoros, Andrew S Allen, David B Goldstein
Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics. PloS one 12 (8) (2017)