Yong-Han Hank Cheng (Yong-Han H Cheng, Y H Hank Cheng)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 11

Top Topics

Amyotrophic Lateral Sclerosis

Endothelial Cells

Top Venues

Nature communications

Journal of medical genetics

bioRxiv : the preprint server for biology

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

Publications

Yong-Han Hank Cheng, Stephanie C Bohaczuk, Andrew Ben Stergachis
Functional categorization of gene regulatory variants that cause Mendelian conditions. Human genetics 143 (4) (2024)
Yong-Han Hank Cheng, Stephanie C Bohaczuk, Andrew Ben Stergachis
Functional categorization of gene regulatory variants that cause Mendelian conditions. Human genetics 143 (4) (2024)
Marta Garcia-Montojo, Saeed Fathi, Cyrus Rastegar, Elena Rita Simula, Tara T Doucet-O'Hare, Yong-Han Hank Cheng, Rachel P M Abrams, Nicholas Pasternack, Nasir Malik, Muzna Bachani, Brianna Disanza, Dragan Maric, Myoung-Hwa Lee, Herui Wang, Ulisses Santamaria, Wenxue Li, Kevon Sampson, Juan Ramiro Lorenzo, Ignacio E Sanchez, Alexandre Mezghrani, Yan Li, Leonardo Antonio Sechi, Sergio Sebastian Pineda, Myriam Heiman, Manolis Kellis, Joseph Steiner, Avindra Nath
TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression. Nature communications 15 (1) (2024)
Yong-Han Hank Cheng, Stephanie C Bohaczuk, Andrew Ben Stergachis
Functional categorization of gene regulatory variants that cause Mendelian conditions. Human genetics 143 (4) (2024)
Marta Garcia-Montojo, Saeed Fathi, Cyrus Rastegar, Elena Rita Simula, Tara T Doucet-O'Hare, Yong-Han Hank Cheng, Rachel P M Abrams, Nicholas Pasternack, Nasir Malik, Muzna Bachani, Brianna Disanza, Dragan Maric, Myoung-Hwa Lee, Herui Wang, Ulisses Santamaria, Wenxue Li, Kevon Sampson, Juan Ramiro Lorenzo, Ignacio E Sanchez, Alexandre Mezghrani, Yan Li, Leonardo Antonio Sechi, Sergio Sebastian Pineda, Myriam Heiman, Manolis Kellis, Joseph Steiner, Avindra Nath
TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression. Nature communications 15 (1) (2024)
Yong-Han Hank Cheng, Stephanie C Bohaczuk, Andrew Ben Stergachis
Functional categorization of gene regulatory variants that cause Mendelian conditions. Human genetics 143 (4) (2024)
Marta Garcia-Montojo, Saeed Fathi, Cyrus Rastegar, Elena Rita Simula, Tara T Doucet-O'Hare, Yong-Han Hank Cheng, Rachel P M Abrams, Nicholas Pasternack, Nasir Malik, Muzna Bachani, Brianna Disanza, Dragan Maric, Myoung-Hwa Lee, Herui Wang, Ulisses Santamaria, Wenxue Li, Kevon Sampson, Juan Ramiro Lorenzo, Ignacio E Sanchez, Alexandre Mezghrani, Yan Li, Leonardo Antonio Sechi, Sergio Sebastian Pineda, Myriam Heiman, Manolis Kellis, Joseph Steiner, Avindra Nath
TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression. Nature communications 15 (1) (2024)
Yong-Han Hank Cheng, Stephanie C Bohaczuk, Andrew Ben Stergachis
Functional categorization of gene regulatory variants that cause Mendelian conditions. Human genetics (2024)
Marta Garcia-Montojo, Saeed Fathi, Cyrus Rastegar, Elena Rita Simula, Tara T Doucet-O'Hare, Yong-Han Hank Cheng, Rachel P M Abrams, Nicholas Pasternack, Nasir Malik, Muzna Bachani, Brianna Disanza, Dragan Maric, Myoung-Hwa Lee, Herui Wang, Ulisses Santamaria, Wenxue Li, Kevon Sampson, Juan Ramiro Lorenzo, Ignacio E Sanchez, Alexandre Mezghrani, Yan Li, Leonardo Antonio Sechi, Sergio Sebastian Pineda, Myriam Heiman, Manolis Kellis, Joseph Steiner, Avindra Nath
TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression. Nature communications 15 (1) (2024)
Mitchell R Vollger, Jonas Korlach, Kiara C Eldred, Elliott G Swanson, Jason G Underwood, Yong-Han Hank Cheng, Jane Ranchalis, Yizi Mao, Elizabeth E Blue, Ulrike Schwarze, Katherine M Munson, Christopher T Saunders, Aaron M Wenger, Aimee Allworth, Sirisak Chanprasert, Brittney L Duerden, Ian Glass, Martha Horike-Pyne, Michelle Kim, Kathleen A Leppig, Ian J McLaughlin, Jessica Ogawa, Elisabeth A Rosenthal, Sam Sheppeard, Stephanie M Sherman, Samuel Strohbehn, Amy L Yuen, null null, null null, Thomas A Reh, Peter H Byers, Michael J Bamshad, Fuki M Hisama, Gail P Jarvik, Yasemin Sancak, Katrina M Dipple, Andrew Ben Stergachis
Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition. bioRxiv : the preprint server for biology (2023)
Valentina Serpieri, Fulvio D'Abrusco, Jennifer C Dempsey, Yong-Han Hank Cheng, Filippo Arrigoni, Janice Baker, Roberta Battini, Enrico Silvio Bertini, Renato Borgatti, Angela K Christman, Cynthia Curry, Stefano D'Arrigo, Joel Fluss, Michael Freilinger, Simone Gana, Gisele E Ishak, Vincenzo Leuzzi, Hailey Loucks, Filippo Manti, Nancy Mendelsohn, Laura Merlini, Caitlin V Miller, Ansar Muhammad, Sara Nuovo, Ludovica Pasca, Wolfgang Schmidt, Sabrina Signorini, Sabrina Siliquini, Krzysztof Szczaluba, Gessica Vasco, Meredith Wilson, Ginevra Zanni, Eugen Boltshauser, Dan Doherty, Enza Maria Valente, null null
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum. Journal of medical genetics (2021)