基本信息
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Career Trajectory
Bio
he developed genomic mismatch scanning and initiated the lab development of DNA microarrays for genomic applications. At UCLA, Prof. Nelson has continued to be interested in technology development and application of genomics to cancer biology and common human diseases with active research areas in Autism, ADHD, vertigo and brain cancers. He developed and led the first genomics core on UCLA campus ( UCLA DNA Microarray Facility). He led the whole genome expression array analysis for the NIH Neuroscience Blueprint. With a team in Pathology and Pediatrics, he implemented whole exome sequencing for clinical purposes in 2011. He formed the Center for Duchenne Muscular Dystrophy in 2007 with Drs. Miceli and Spencer that has grown into a unique center that provides coordinated patient care, access to clinical trials, translational and basic research, and educational opportunities on campus. In 2014, he initiated with others, the Undiagnosed Diseases Network UCLA Clinical Site to improve diagnosis of individuals with difficult to diagnose genetic disorders. His laboratory continues to develop and use genomic technology to pursue biological insights that lead to new therapeutic interventions in humans.
Research Interests
Papers共 470 篇Author StatisticsCo-AuthorSimilar Experts
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Igor Z Barjaktarevic, Andrew W Hong, Alyssa Hoover,Stanley Nelson,Said Isse, Semi Yoon,Mark Brantley
Gloria K. E. Zodanu,John H. Hwang,Zubin Mehta,Carlos Sisniega, Alexander Barsegian,Xuedong Kang,Reshma Biniwale,Ming-Sing Si,Gary M. Satou,Nancy Halnon,Wayne W. Grody,Glen S. Van Arsdell,Stanley F. Nelson,Marlin Touma
International Journal of Molecular Sciencesno. 10 (2024): 5469-5469
Marie Morimoto,Eunjin Ryu, Benjamin J. Steger,Abhijit Dixit,Yoshihiko Saito, Juyeong Yoo,Amelie T. van der Ven,Natalie Hauser,Peter J. Steinbach,Kazumasa Oura,Alden Y. Huang,Fanny Kortum,Shinsuke Ninomiya,Elisabeth A. Rosenthal, Hannah K. Robinson, Katie Guegan,Jonas Denecke, Sankarasubramoney H. Subramony, Callie J. Diamonstein,Jie Ping, Mark Fenner, Elsa Balton, Sam Strohbehn,Aimee Allworth,Michael J. Bamshad, Mahi Gandhi,Katrina M. Dipple,Elizabeth E. Blue,Gail P. Jarvik,C. Christopher Lau,Ingrid A. Holm,Monika Weisz-Hubshman, Benjamin D. Solomon,Stanley F. Nelson,Ichizo Nishino,David R. Adams,Sukhyun Kang,William A. Gahl,Camilo Toro,Kyungjae Myung,May Christine V. Malicdan
The American Journal of Human Genetics (2024)
Shilpa Nadimpalli Kobren, Mikhail A Moldovan,Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum,Alexander Veit,Rosario I Corona, George de V Carvalho Neto, Julian Willett,Michele Berselli,William Ronchetti,Stanley F Nelson, Julian A Martinez-Agosto,Richard Sherwood,Joel Krier,Isaac S Kohane,Undiagnosed Diseases Network,Shamil R Sunyaev
bioRxiv the preprint server for biology (2024)
Aravindhan Veerapandiyan,Anne M. Connolly,Katherine D. Mathews,Stanley Nelson,Craig McDonald,Richard S. Finkel, Vettaikorumakankav Vedanarayanan,Cuixia Tian,Susan Apkon,Julie A. Parsons,Jonathan H. Soslow,William Bryan Burnette, Kaitlin Y. Batley,Susan T. Iannaccone,Carolina Tesi Rocha,Kevin M. Flanigan,Diana Bharucha‐Goebel, Sarah Wright,Migvis Monduy,Simona Treidler,Ashutosh Kumar,Nancy L. Kuntz,Vamshi K. Rao,Rachel Schrader,Saunder M. Bernes,Vikki Ann Stefans,Jena M. Krueger,Marcia V. Felker, Omer Abdul Hamid,Arpita Lakhotia,Susan Matesanz,Partha S. Ghosh, Natalie Katz,Hoda Abdel‐Hamid,Chamindra G. Laverty,Bo Hoon Lee,Amy Harper, Leigh Ramos‐Platt,Diana Castro,Russell J. Butterfield,Crystal M. Proud,Craig M. Zaidman,Emma Ciafaloni
Annals of the Child Neurology Societyno. 3 (2024): 184-188
Lauren Jeffries,Emily K. Mis,Kirsty McWalter,Sandra Donkervoort,Nina N. Brodsky,Jean-Marie Carpier,Weizhen Ji, Cristian Ionita,Bhaskar Roy,Jon S. Morrow,Armine Darbinyan,Krishna Iyer,Ritu B. Aul,Siddharth Banka,Katherine R. Chao, Laura Cobbold,Stacey Cohen,Helena M. Custodio,Margaret Drummond-Borg,Frances Elmslie,Erika Finanger,Bryan E. Hainline,Ingo Helbig,Stacy Hewson,Ying Hu,Adam Jackson,Dragana Josifova,Monica Konstantino,Meganne E. Leach, Bryan Mak,David McCormick, Elisabeth McGee,Stanley Nelson,Joanne Nguyen,Kimberly Nugent, Lucy Ortega,Howard P. Goodkin,Elizabeth Roeder,Sani Roy,Katie Sapp,Dimah Saade,Sanjay M. Sisodiya,Karen Stals,Shelley Towner,William Wilson,Mustafa K. Khokha,Carsten G. Boennemann,Carrie L. Lucas,Saquib A. Lakhani
Elise Pisan,Chiara De Luca,Francesco Brancati,Rossana Sanchez Russo,Dong Li,Elizabeth Bhoj,Tara Wenger,Ashish Marwaha,Nicole Johnson,Claire Beneteau,Elise Brischoux -Boucher,Gunnar Houge,Julie Paulsen,Trine Bjorg Hammer,Jakob Ek,Daniela Schweitzer,Bianca E. Russell,Marina Dutra-Clarke,Stanley Nelson,Emilie D. Douine,Rosario I. Corona,Tracy Dudding, Hannah Thomson,Karen Low,Newell Belnap,Maria Iascone,Manuela Priolo,Diana Carli,Alessandro Mussa,Emilia K. Bijlsma,Nathan Kopp, Jean-Philippe Jais,Jeanne Amiel, Christopher T. Gordona
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAno. 12 (2024): e2317601121-e2317601121
Yue Huang,Kristy L. Jay,Alden Yen-Wen Huang,Jijun Wan,Sharayu V. Jangam,Odelia Chorin,Annick Rothschild,Ortal Barel,Milena Mariani,Maria Iascone,Han Xue, Jing Huang,Cyril Mignot,Boris Keren,Virginie Saillour, Annelise Y. Mah-Som,Stephanie Sacharow,Farrah Rajabi,Carrie Costin,Shinya Yamamoto,Oguz Kanca,Hugo J. Bellen,Jill A. Rosenfeld,Christina G. S. Palmer,Stanley F. Nelson, Michael F. Wangler, Julian A. Martinez-Agosto
GENETICS IN MEDICINEno. 11 (2024)
Elise Pisan,Chiara De Luca,Francesco Brancati,Rossana Sanchez Russo, Dong Liu,Elizabeth Bhoj,Tara Wenger,Ashish Marwaha,Nicole Johnson,Claire Bénéteau,Elise Brischoux‐Boucher,Gunnar Houge,Julie Paulsen,Trine Bjørg Hammer,Jakob Ek,Daniela N. Schweitzer,Bianca Russell,Marina Dutra‐Clarke,Stanley F. Nelson,Emilie D. Douine,Rosario I. Corona,Tracy Dudding, Hannah Thomson,Karen Low,Newell Belnap,Maria Iascone,Manuela Priolo,Diana Carli,Alessandro Mussa,Emilia K. Bijlsma,Nicolas Kopp, Jean‐Philippe Jaïs,Jeanne Amiel,Christopher T. Gordon
Proceedings of the National Academy of Sciences of the United States of Americano. 12 (2024)
AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 11 (2024)
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Author Statistics
#Papers: 474
#Citation: 45730
H-Index: 105
G-Index: 209
Sociability: 9
Diversity: 4
Activity: 62
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