Yao Yu
发表
XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets
P. Scheet,
M. Yandell,
C. Huff,
2017,
Nucleic acids research.
Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignancies
P. Jia,
M. Hung,
C. Huff,
2022,
Proceedings of the National Academy of Sciences of the United States of America.
P. Scheet,
C. Huff,
Hao Hu,
2020,
Journal of Medical Genetics.
R. Vierkant,
E. Goode,
N. Traficante,
2019,
Journal of Medical Genetics.
C. Huff,
E. Shpall,
Yao Yu,
2022,
Leukemia.
Martin A. M. Reijns,
J. Rosenfeld,
Sancha Martin,
2018,
American journal of human genetics.
Amber M. Johnson,
Ann M. Bailey,
F. Meric-Bernstam,
2018,
Journal of the National Cancer Institute.
Olivier Lichtarge,
Predrag Radivojac,
Emidio Capriotti,
2019,
Human mutation.
L. Cannon-Albright,
S. Tavtigian,
C. Huff,
2019,
bioRxiv.
L. Cannon-Albright,
J. Farnham,
Alun Thomas,
2018,
Journal of the National Cancer Institute.
Richard G. Fowler,
P. Scheet,
M. Tetzlaff,
2018,
Clinical Cancer Research.
A. Moon,
C. Huff,
A. Welm,
2021,
Cell reports.
P. Scheet,
L. Cannon-Albright,
J. Gu,
2021,
Human Genetics and Genomics Advances.
P. Scheet,
C. Huff,
Hao Hu,
2018,
Biochimica et biophysica acta. Molecular basis of disease.
A. Moon,
C. Huff,
B. Delisle,
2019,
Pediatric Cardiology.
L. Hood,
J. Roach,
L. Jorde,
2017,
PLoS genetics.
Y. Liu,
P. Jia,
S. Chiou,
2023,
Nature Communications.
J. Lupski,
R. Gibbs,
S. Jhangiani,
2015,
Fertility and sterility.
P. Scheet,
K. Chang,
C. Huff,
2019,
Nature Biotechnology.
A. Moon,
C. Huff,
B. Delisle,
2019,
Pediatric Cardiology.