Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets

by Jedidiah Carlson, Jun Z. Li, Sebastian Zöllner
Published 2018-11-01

ALKALI EXTRACTION OF POLYSACCHARIDES FROM PROSO MILLET AND ANTIOXIDANT ACTIVITY

by AI S. ZHU, MAO Q. XU, JUN Z. ZHAO
Published 2017-12-01

Impact of between-tissue differences on pan-cancer predictions of drug sensitivity.

by John P Lloyd, Matthew B Soellner, Sofia D Merajver, Jun Z Li
Published 2021-02-01

P-Type Tunnel FETs With Triple Heterojunctions

by Jun Z. Huang, Pengyu Long, Michael Povolotskyi, Gerhard Klimeck, Mark J. W. Rodwell
Published 2016-01-01

EXPERIMENTATION AND MODELLING FOR COLOCASIA ESCULENTA (L.) SCHOOT SLICES DRYING PROCESS

by AI S. ZHU, YAN W. SHI, DA Z. TAO, MAO Q. XU, JUN Z. ZHAO
Published 2019-06-01

Genetic analysis of a rat model of aerobic capacity and metabolic fitness.

by Yu-Yu Ren, Katherine A Overmyer, Nathan R Qi, Mary K Treutelaar, Lori Heckenkamp, Molly Kalahar, Lauren G Koch, Steven L Britton, Charles F Burant, Jun Z Li
Published 2013-01-01

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

by Jedidiah Carlson, Adam E. Locke, Matthew Flickinger, Matthew Zawistowski, Shawn Levy, Richard M. Myers, Michael Boehnke, Hyun Min Kang, Laura J. Scott, Jun Z. Li, Sebastian Zöllner, The BRIDGES Consortium
Published 2018-09-01

Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.

by Sophie I Candille, Devin M Absher, Sandra Beleza, Marc Bauchet, Brian McEvoy, Nanibaa' A Garrison, Jun Z Li, Richard M Myers, Gregory S Barsh, Hua Tang, Mark D Shriver
Published 2012-01-01

Inference of cell type content from human brain transcriptomic datasets illuminates the effects of age, manner of death, dissection, and psychiatric diagnosis.

by Megan Hastings Hagenauer, Anton Schulmann, Jun Z Li, Marquis P Vawter, David M Walsh, Robert C Thompson, Cortney A Turner, William E Bunney, Richard M Myers, Jack D Barchas, Alan F Schatzberg, Stanley J Watson, Huda Akil
Published 2018-01-01

Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing

by Fernanda A. Correa, Marcela M. França, Qing Fang, Qianyi Ma, Tania A. Bachega, Andresa Rodrigues, Bilge A. Ozel, Jun Z. Li, Berenice B. Mendonca, Alexander A. L. Jorge, Luciani R. Carvalho, Sally A. Camper, Ivo J. P Arnhold

Sample matching by inferred agonal stress in gene expression analyses of the brain

by Bunney William E, Chung Tisha, Shokoohi Vida, Walsh David, Vawter Marquis P, Tomita Hiroaki, Choudary Prabhakara V, Evans Simon J, Tsavaler Larisa, Meng Fan, Li Jun Z, Jones Edward G, Akil Huda, Watson Stanley J, Myers Richard M
Published 2007-09-01

Murine models of IDH-wild-type glioblastoma exhibit spatial segregation of tumor initiation and manifestation during evolution

by Yinghua Li, Bo Li, Wei Li, Yuan Wang, Seçkin Akgül, Daniel M. Treisman, Kevin A. Heist, Brianna R. Pierce, Benjamin Hoff, Cheng-Ying Ho, David O. Ferguson, Alnawaz Rehemtulla, Siyuan Zheng, Brian D. Ross, Jun Z. Li, Yuan Zhu
Published 2020-07-01

TCF21+ mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice

by Yu-chi Shen, Adrienne Niederriter Shami, Lindsay Moritz, Hailey Larose, Gabriel L. Manske, Qianyi Ma, Xianing Zheng, Meena Sukhwani, Michael Czerwinski, Caleb Sultan, Haolin Chen, Stephen J. Gurczynski, Jason R. Spence, Kyle E. Orwig, Michelle Tallquist, Jun Z. Li, Saher Sue Hammoud
Published 2021-06-01

Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay

by Myungjin Kim, Erin Sandford, Damian Gatica, Yu Qiu, Xu Liu, Yumei Zheng, Brenda A Schulman, Jishu Xu, Ian Semple, Seung-Hyun Ro, Boyoung Kim, R Nehir Mavioglu, Aslıhan Tolun, Andras Jipa, Szabolcs Takats, Manuela Karpati, Jun Z Li, Zuhal Yapici, Gabor Juhasz, Jun Hee Lee, Daniel J Klionsky, Margit Burmeister
Published 2016-01-01

Post-mortem molecular profiling of three psychiatric disorders

by Ryne C. Ramaker, Kevin M. Bowling, Brittany N. Lasseigne, Megan H. Hagenauer, Andrew A. Hardigan, Nicholas S. Davis, Jason Gertz, Preston M. Cartagena, David M. Walsh, Marquis P. Vawter, Edward G. Jones, Alan F. Schatzberg, Jack D. Barchas, Stanley J. Watson, Blynn G. Bunney, Huda Akil, William E. Bunney, Jun Z. Li, Sara J. Cooper, Richard M. Myers
Published 2017-07-01

G Protein-Linked Signaling Pathways in Bipolar and Major Depressive Disorders

by Hiroaki eTomita, Hiroaki eTomita, Mary E Ziegler, Helen B Kim, Simon J Evans, Prabhakara V Choudary, Jun Z Li, Fan eMeng, Manhong eDai, Charles R Neal, Richard M Myers, Terry P Speed, Jack D Barchas, Alan F Schatzberg, Stanley J Watson, Huda eAkil, Edward G Jones, William E Bunney, Marquis P Vawter
Published 2013-12-01

Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum

by Marilena Nakaguma, Nathalia Garcia Bianchi Pereira Ferreira, Anna Flavia Figueredo Benedetti, Mariana Cotarelli Madi, Juliana Moreira Silva, Jun Z. Li, Qianyi Ma, Ayse Bilge Ozel, Qing Fang, Amanda de Moraes Narcizo, Laís Cavalca Cardoso, Luciana Ribeiro Montenegro, Mariana Ferreira de Assis Funari, Mirian Yumie Nishi, Ivo Jorge Prado Arnhold, Alexander Augusto de Lima Jorge, Berenice Bilharinho de Mendonca, Sally Ann Camper, Luciani R. Carvalho
Published 2021-07-01

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

by Jacqueline Saw, Min-Lee Yang, Mark Trinder, Catherine Tcheandjieu, Chang Xu, Andrew Starovoytov, Isabelle Birt, Michael R. Mathis, Kristina L. Hunker, Ellen M. Schmidt, Linda Jackson, Natalia Fendrikova-Mahlay, Matthew Zawistowski, Chad M. Brummett, Sebastian Zoellner, Alexander Katz, Dawn M. Coleman, Kirby Swan, Christopher J. O’Donnell, Million Veteran Program, Xiang Zhou, Jun Z. Li, Heather L. Gornik, Themistocles L. Assimes, James C. Stanley, Liam R. Brunham, Santhi K. Ganesh
Published 2020-09-01

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.

by Sarah J Garnai, Michelle L Brinkmeier, Ben Emery, Tomas S Aleman, Louise C Pyle, Biliana Veleva-Rotse, Robert A Sisk, Frank W Rozsa, Ayse Bilge Ozel, Jun Z Li, Sayoko E Moroi, Steven M Archer, Cheng-Mao Lin, Sarah Sheskey, Laurel Wiinikka-Buesser, James Eadie, Jill E Urquhart, Graeme C M Black, Mohammad I Othman, Michael Boehnke, Scot A Sullivan, Gregory L Skuta, Hemant S Pawar, Alexander E Katz, Laryssa A Huryn, Robert B Hufnagel, Genomic Ascertainment Cohort, Sally A Camper, Julia E Richards, Lev Prasov
Published 2019-05-01