檢索結果 - Lohith Madireddy
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Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls 由 Dorothee Nickles, Hsuan P. Chen, Michael Li, Pouya Khankhanian, Lohith Madireddy, Stacy J. Caillier, Adam Santaniello, Bruce Cree, Daniel Pelletier, Stephen L. Hauser, Jorge R. Oksenberg, Sergio E. Baranzini
出版 2013Artigo -
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Expression profiling of Aldh1l1‐precursors in the developing spinal cord reveals glial lineage‐specific genes and direct Sox9‐Nfe2l1 interactions 由 Anna V. Molofsky, Stacey M. Glasgow, Lesley Chaboub, Hui‐Hsin Tsai, Alice T. Murnen, Kevin W. Kelley, Stephen P.J. Fancy, Tracy J. Yuen, Lohith Madireddy, Sergio E. Baranzini, Benjamin Deneen, David H. Rowitch, Michael C. Oldham
出版 2013Artigo -
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Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis 由 Xiaoming Jia, Lohith Madireddy, Stacy J. Caillier, Adam Santaniello, Federica Esposito, Gıancarlo Comı, Olaf Stüve, Yuan Zhou, Bruce Taylor, Trevor J. Kilpatrick, Filippo Martinelli Boneschi, Bruce Cree, Jorge R. Oksenberg, Stephen L. Hauser, Sergio E. Baranzini
出版 2018Artigo -
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An ImmunoChip study of multiple sclerosis risk in African Americans 由 Noriko Isobe, Lohith Madireddy, Pouya Khankhanian, Takuya Matsushita, Stacy J. Caillier, Jayaji M. Moré, Pierre‐Antoine Gourraud, Jacob L. McCauley, Ashley Beecham, Laura Piccio, Joseph Herbert, Omar Khan, Jeffrey A. Cohen, Lael A. Stone, Adam Santaniello, Bruce Cree, Suna Önengüt-Gümüşcü, Stephen S. Rich, Stephen L. Hauser, Stephen Sawcer, Jorge R. Oksenberg
出版 2015Artigo -
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Classification of neurological diseases using multi-dimensional CSF analysis 由 Catharina C. Groß, Andreas Schulte‐Mecklenbeck, Lohith Madireddy, Marc Pawlitzki, Christine Strippel, Saskia Räuber, Julia Krämer, Leoni Rolfes, Tobias Ruck, Carolin Beuker, Antje Schmidt‐Pogoda, Lisa Lohmann, Tilman Schneider‐Hohendorf, Tim Hahn, Nicholas Schwab, Jens Minnerup, Nico Melzer, Luisa Klotz, Sven G. Meuth, Gerd Meyer zu Hörste, Sergio E. Baranzini, Heinz Wiendl
出版 2021Artigo -
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Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1 由 Anne Slavotinek, Sergio E. Baranzini, Denny Schanze, Cassandre Labelle‐Dumais, Kieran M. Short, Richard C. Chao, Mani Yavi, Emilia K. Bijlsma, Catherine Chu, Stacy L. Musone, Amanda Wheatley, Pui‐Yan Kwok, Sandra L. Marles, J. P. Fryns, A. Murat Maga, Mohamed G. Hassan, Douglas B. Gould, Lohith Madireddy, Chumei Li, Timothy C. Cox, Ian Smyth, Albert E. Chudley, Martin Zenker
出版 2011Artigo -
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Exome sequencing in 32 patients with anophthalmia/microphthalmia and developmental eye defects 由 Anne Slavotinek, Sarah Garcia, Gemma Chandratillake, Tanya Bardakjian, Ehsan Ullah, Di Wu, Kaoru Umeda, R. Lao, Paul Ling-Fung Tang, Eunice Wan, Lohith Madireddy, Svetlana Lyalina, Bryce A. Mendelsohn, Shannon Dugan, Jeanie Tirch, R. Tischler, Jason Harris, Michael J. Clark, Stephen A. Chervitz, A. Patwardhan, John West, Philip C. Ursell, Alejandra de Alba Campomanes, Adele Schneider, Pui‐Yan Kwok, Sergio E. Baranzini, R.O. Chen
出版 2014Artigo -
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A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis 由 Lohith Madireddy, Nikolaos A. Patsopoulos, Chris Cotsapas, Steffan D. Bos, Ashley Beecham, Jacob L. McCauley, Kicheol Kim, Xiaoming Jia, Adam Santaniello, Stacy J. Caillier, Till F. M. Andlauer, Lisa F. Barcellos, Tone Berge, Luisa Bernardinelli, Filippo Martinelli Boneschi, David R. Booth, Farren Briggs, Elisabeth Gulowsen Celius, Manuel Comabella, Giacomo P. Comi, Bruce Cree, Sandra D’Alfonso, Katrina Dedham, Pierre Duquette, Efthimios Dardiotis, Federica Esposito, Bertrand Fontaine, Christiane Gasperi, An Goris, Bénédicte Dubois, Pierre‐Antoine Gourraud, Georgios Hadjigeorgiou, Jonathan L. Haines, Clive Hawkins, Bernhard Hemmer, Rogier Hintzen, Dana Horáková, Noriko Isobe, Seema Kalra, Jun‐ichi Kira, Michael Khalil, Ingrid Kockum, Christina M. Lill, Matthew R. Lincoln, Felix Luessi, Roland Martinꝉ, Annette Oturai, Aarno Palotie, Margaret A. Pericak‐Vance, Roland G. Henry, Janna Saarela, Adrian J. Ivinson, Tomas Olsson, Bruce Taylor, Graeme J. Stewart, Hanne F. Harbo, Alastair Compston, Stephen L. Hauser, D Hafler, Frauke Zipp, Philip L. De Jager, Stephen Sawcer, Jorge R. Oksenberg, Sergio E. Baranzini
出版 2019Revisão
相關主題
Biology
Gene
Genetics
Medicine
Immunology
Multiple sclerosis
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Anophthalmia
Central nervous system
Computational biology
Gene expression
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Microphthalmia
Neuroscience
Phenotype
African american
Allele
Anal atresia
Anatomy
Astrocyte
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Atresia
Autoimmunity
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CHARGE syndrome
Cell fate determination
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