Articles with public access mandates - Yujun HanLearn more
Available somewhere: 15
The B73 maize genome: complexity, diversity, and dynamics
PS Schnable, D Ware, RS Fulton, JC Stein, F Wei, S Pasternak, C Liang, ...
science 326 (5956), 1112-1115, 2009
Mandates: US National Institutes of Health
De novo mutations in epileptic encephalopathies
Nature 501 (7466), 217-221, 2013
Mandates: US National Institutes of Health
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
Mandates: US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1267-1288, 2018
Mandates: US National Institutes of Health, US Department of Veterans Affairs, Howard …
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios
X Zhu, S Petrovski, P Xie, EK Ruzzo, YF Lu, K McSweeney, B Ben-Zeev, ...
Genetics in Medicine 17 (10), 774-781, 2015
Mandates: US National Institutes of Health, National Health and Medical Research …
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
Mandates: US National Institutes of Health
Using ERDS to infer copy-number variants in high-coverage genomes
M Zhu, AC Need, Y Han, D Ge, JM Maia, Q Zhu, EL Heinzen, ET Cirulli, ...
The American Journal of Human Genetics 91 (3), 408-421, 2012
Mandates: US National Institutes of Health
The intolerance of regulatory sequence to genetic variation predicts gene dosage sensitivity
S Petrovski, AB Gussow, Q Wang, M Halvorsen, Y Han, WH Weir, ...
PLoS genetics 11 (9), e1005492, 2015
Mandates: US National Institutes of Health, National Health and Medical Research …
Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis
GM DeStefano, KA Fantauzzo, L Petukhova, M Kurban, M Tadin-Strapps, ...
Proceedings of the National Academy of Sciences 110 (19), 7790-7795, 2013
Mandates: US National Institutes of Health
TARGeT: a web-based pipeline for retrieving and characterizing gene and transposable element families from genomic sequences
Y Han, JM Burnette III, SR Wessler
Nucleic acids research 37 (11), e78-e78, 2009
Mandates: Howard Hughes Medical Institute
Noncoding deletions reveal a gene that is critical for intestinal function
D Oz-Levi, T Olender, I Bar-Joseph, Y Zhu, D Marek-Yagel, I Barozzi, ...
Nature 571 (7763), 107-111, 2019
Mandates: US Department of Energy, US National Institutes of Health
Incorporating functional information in tests of excess de novo mutational load
Y Jiang, Y Han, S Petrovski, K Owzar, DB Goldstein, AS Allen
The American Journal of Human Genetics 97 (2), 272-283, 2015
Mandates: US National Institutes of Health
Systematic assessment of imputation performance using the 1000 Genomes reference panels
Q Liu, ET Cirulli, Y Han, S Yao, S Liu, Q Zhu
Briefings in bioinformatics 16 (4), 549-562, 2015
Mandates: US National Institutes of Health
Utilizing population controls in rare-variant case-parent association tests
Y Jiang, GA Satten, Y Han, MP Epstein, EL Heinzen, DB Goldstein, ...
The American Journal of Human Genetics 94 (6), 845-853, 2014
Mandates: US National Institutes of Health
A Sequence Assembler That Masks Exact Repeats Identified from the shotgun Data
GK Wong, J Hu, Y Han, J He, L Tao, J Wang, L Cong, C Ye, X Huang, ...
Mandates: US National Institutes of Health, Chinese Academy of Sciences, National …
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