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Richard H Finnell (Richard Finnell, R H Finnell)

Scopus Author ID ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 20

Top Venues

Baylor College of Medicine

Oregon Health & Science University (PHD)

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

Affiliation History

Baylor College of Medicine Aug 20o 2017

United States

Professor :: Molecular and Cellular Biology and Medicine

Education History

Oregon Health & Science University Sep 1o 1978 - Jun 1o 1980

United States

PHD :: Medical Genetics

Publications

Richard H Finnell, Huiping Zhu
Periconceptional maternal folate supplementation impacts a diverse range of congenital malformations. Pediatric research (2023)
Ainara Cano, Mercedes Vazquez-Chantada, Javier Conde-Vancells, Aintzane Gonzalez-Lahera, David Mosen-Ansorena, Francisco J Blanco, Karine Clément, Judith Aron-Wisnewsky, Albert Tran, Philippe Gual, Carmelo García-Monzón, Joan Caballería, Azucena Castro, María Luz Martínez-Chantar, José M Mato, Huiping Zhu, Richard H Finnell, Ana Mª Aransay
Impaired Function of Solute Carrier Family 19 Leads to Low Folate Levels and Lipid Droplet Accumulation in Hepatocytes. Biomedicines 11 (2) (2023)
Pagna Sok, Aniko Sabo, Lynn M Almli, Mary M Jenkins, Wendy N Nembhard, A J Agopian, Michael J Bamshad, Elizabeth E Blue, Lawrence C Brody, Austin L Brown, Marilyn L Browne, Mark A Canfield, Suzan L Carmichael, Jessica X Chong, Shannon Dugan-Perez, Marcia L Feldkamp, Richard H Finnell, Richard A Gibbs, Denise M Kay, Yunping Lei, Qingchang Meng, Cynthia A Moore, James C Mullikin, Donna Muzny, Andrew F Olshan, Faith Pangilinan, Jennita Reefhuis, Paul A Romitti, Jeremy M Schraw, Gary M Shaw, Martha M Werler, Sanjiv Harpavat, Philip J Lupo, null null
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. American journal of medical genetics. Part A (2023)
Bernard K van der Veer, Lehua Chen, Colin Custers, Paraskevi Athanasouli, Mariana Schroiff, Riet Cornelis, Jonathan Sai-Hong Chui, Richard H Finnell, Frederic Lluis, Kian Peng Koh
Dual functions of TET1 in germ layer lineage bifurcation distinguished by genomic context and dependence on 5-methylcytosine oxidation. Nucleic acids research (2023)
Xuanye Cao, Jianfeng Xu, Ying L Lin, Robert M Cabrera, Qiuying Chen, Chaofan Zhang, John W Steele, Xiao Han, Steven S Gross, Bogdan J Wlodarczyk, James R Lupski, Weibo Xie, Hongyan Wang, Richard H Finnell, Yunping Lei
Excess folic acid intake increases DNA de novo point mutations. Cell discovery 9 (1) (2023)
Xuanye Cao, Jianfeng Xu, Ying L Lin, Robert M Cabrera, Qiuying Chen, Chaofan Zhang, John W Steele, Xiao Han, Steven S Gross, Bogdan J Wlodarczyk, James R Lupski, Weibo Xie, Hongyan Wang, Richard H Finnell, Yunping Lei
Excess folic acid intake increases DNA de novo point mutations. Cell discovery 9 (1) (2023)
Ainara Cano, Mercedes Vazquez-Chantada, Javier Conde-Vancells, Aintzane Gonzalez-Lahera, David Mosen-Ansorena, Francisco J Blanco, Karine Clément, Judith Aron-Wisnewsky, Albert Tran, Philippe Gual, Carmelo García-Monzón, Joan Caballería, Azucena Castro, María Luz Martínez-Chantar, José M Mato, Huiping Zhu, Richard H Finnell, Ana Mª Aransay
Impaired Function of Solute Carrier Family 19 Leads to Low Folate Levels and Lipid Droplet Accumulation in Hepatocytes. Biomedicines 11 (2) (2023)
Ainara Cano, Mercedes Vazquez-Chantada, Javier Conde-Vancells, Aintzane Gonzalez-Lahera, David Mosen-Ansorena, Francisco J Blanco, Karine Clément, Judith Aron-Wisnewsky, Albert Tran, Philippe Gual, Carmelo García-Monzón, Joan Caballería, Azucena Castro, María Luz Martínez-Chantar, José M Mato, Huiping Zhu, Richard H Finnell, Ana Mª Aransay
Impaired Function of Solute Carrier Family 19 Leads to Low Folate Levels and Lipid Droplet Accumulation in Hepatocytes. Biomedicines 11 (2) (2023)
Xiao Han, Xuanye Cao, Vanessa Aguiar-Pulido, Wei Yang, Menuka Karki, Paula Andrea Pimienta Ramirez, Robert M Cabrera, Ying Linda Lin, Bogdan J Wlodarczyk, Gary M Shaw, Margaret Elizabeth Ross, Cui-Lian Zhang, Richard H Finnell, Yunping Lei
CIC missense variants contribute to susceptibility for spina bifida. Human mutation (2022)
Nithya Lakshmi Mohan Dass, Lorenzo D Botto, Sarah C Tinker, Mark A Canfield, Richard H Finnell, Michael Shayne Gallaway, Syed Shahrukh Hashmi, Adrienne T Hoyt, Wendy N Nembhard, Dorothy Kim Waller, null null
Associations between maternal reports of periconceptional fever from miscellaneous causes and structural birth defects. Birth defects research 114 (15) (2022)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Cuilian Zhang, Vincent T Ramaekers, Richard H Finnell, Yunping Lei
KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology 12 (1) (2022)
Xiao Han, Xuanye Cao, Robert M Cabrera, Paula Andrea Pimienta Ramirez, Cuilian Zhang, Vincent T Ramaekers, Richard H Finnell, Yunping Lei
KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology 12 (1) (2022)
Vanessa Aguiar-Pulido, Paul Wolujewicz, Alexander Martinez-Fundichely, Eran Elhaik, Gaurav Thareja, Alice Abdel Aleem, Nader Chalhoub, Tawny Cuykendall, Jamel Al-Zamer, Yunping Lei, Haitham El-Bashir, James M Musser, Abdulla Al-Kaabi, Gary M Shaw, Ekta Khurana, Karsten Suhre, Christopher E Mason, Olivier Elemento, Richard H Finnell, Margaret Elizabeth Ross
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk. Proceedings of the National Academy of Sciences of the United States of America 118 (51) (2022)
Cristiane Sá Roriz Fonteles, Richard H Finnell, Yunping Lei, Maria E Zurita-Jimenez, A J Monteiro, T M George, R J Harshbarger
De novo ALX4 variant detected in child with non-syndromic craniosynostosis. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 54 (11) (2021)
Abdel Rahman Abdel Fattah, Brian Daza, Gregorius Rustandi, Miguel Ángel Berrocal-Rubio, Benjamin Gorissen, Suresh Poovathingal, Kristofer Davie, Jorge Barrasa-Fano, Mar Cóndor, Xuanye Cao, Derek Hadar Rosenzweig, Yunping Lei, Richard H Finnell, Catherine M Verfaillie, Maurilio Sampaolesi, Peter Dedecker, Hans Van Oosterwyck, Stein Aerts, Adrian Ranga
Actuation enhances patterning in human neural tube organoids. Nature communications 12 (1) (2021)
Xinyu Mei, Dashi Qi, Ting Zhang, Ying Zhao, Li Jin, Junli Hou, Jianhua Wang, Yan Lin, Yang Xu, Pingping Zhu, Ze-Xian Liu, Lei Huang, Ji Nie, Wen Si, Jingyi Ma, Jianhong Ye, Richard H Finnell, Hexige Saiyin, Hong-Yan Wang, Jianyuan Zhao, Shimin Zhao, Wei Xu
Inhibiting MARSs reduces hyperhomocysteinemia-associated neural tube and congenital heart defects. EMBO molecular medicine 12 (3) (2020)
Xuanye Cao, Tian Tian, John W Steele, Robert M Cabrera, Vanessa Aguiar-Pulido, Shruti Wadhwa, Nikitha Bhavani, Patrick Bi, Nick H Gargurevich, Ethan N Hoffman, Chun-Quan Cai, Nicholas J Marini, Wei Yang, Gary M Shaw, Margaret Elizabeth Ross, Richard H Finnell, Yunping Lei
Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida. Human mutation 41 (4) (2020)
Rachel A Keuls, Karin Kojima, Brittney Lozzi, John W Steele, Qiuying Chen, Steven S Gross, Richard H Finnell, Ronald J Parchem
MiR-302 Regulates Glycolysis to Control Cell-Cycle during Neural Tube Closure. International journal of molecular sciences 21 (20) (2020)
Toluwani E Taiwo, Xuanye Cao, Robert M Cabrera, Yunping Lei, Richard H Finnell
Approaches to studying the genomic architecture of complex birth defects. Prenatal diagnosis 40 (9) (2020)
Yunping Lei, Sung-Eun Kim, Zhongzhong Chen, Xuanye Cao, Huiping Zhu, Wei Yang, Gary M Shaw, Yufang Zheng, Ting Zhang, Hong-Yan Wang, Richard H Finnell
Variants identified in PTK7 associated with neural tube defects. Molecular genetics & genomic medicine 7 (4) (2019)

Richard H Finnell.css-eqlu8i{font-size:small;padding-left:4px;} (Richard Finnell, R H Finnell)

Publication Activity (10 Years)

Top Topics

Top Venues

Richard H Finnell (Richard Finnell, R H Finnell)