Yujun Han

发表

Using ERDS to infer copy-number variants in high-coverage genomes.

K. Shianna, D. Ge, A. Need, 2012, American journal of human genetics.

De novo mutations in the classic epileptic encephalopathies

Michael R. Johnson, I. Scheffer, H. Mefford, 2013, Nature.

De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies.

Michael R. Johnson, I. Scheffer, H. Mefford, 2014, American journal of human genetics.

The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity

Ayal B. Gussow, D. Goldstein, A. Allen, 2015, PLoS genetics.

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Brittany N. Lasseigne, W. Chung, D. Goldstein, 2015, Science.

Incorporating Functional Information in Tests of Excess De Novo Mutational Load.

Yujun Han, Kouros Owzar, Andrew S Allen, 2015, American journal of human genetics.

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

Yujun Han, Doron Lancet, Elon Pras, 2015, Genetics in Medicine.

Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013))

Michael R. Johnson, I. Scheffer, H. Mefford, 2017 .

Noncoding Deletions Expose a Novel Gene Critical for Intestinal Function

D. Goldstein, D. Dickel, A. Visel, 2019, Nature.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene in and for Therapeutic

Timothy A. Miller, Denis C. Bauer, Shankaracharya, 2018 .

Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis

V. Jobanputra, Yufeng Shen, Yujun Han, 2013, Proceedings of the National Academy of Sciences of the United States of America.

Efficient direct deoxygenation of bio-oil model compound (anisole) on highly dispersed SiO2-supported Ni3Ga intermetallic compound prepared by direct impregnation-reduction method

Yujun Han, Jixiang Chen, Yinteng Shi, 2021 .

A Bayesian framework for de novo mutation calling in parents-offspring trios

Wei Chen, Yujun Han, Qiang Wei, 2015, Bioinform..

Systematic assessment of imputation performance using the 1000 Genomes reference panels

Qian Liu, Elizabeth T. Cirulli, Yujun Han, 2015, Briefings Bioinform..

Utilizing population controls in rare-variant case-parent association tests.

Yujun Han, Michael P Epstein, Glen A Satten, 2014, American journal of human genetics.

De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies.

H. Mefford, P. May, R. Krause, 2017, American journal of human genetics.

De novo mutations in the classic epileptic encephalopathies

Michael R. Johnson, I. Scheffer, H. Mefford, 2013, Nature.