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Search Results - Tang, Ruen
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Statistical properties of differences between low and high resolution CMAQ runs with matched initial and boundary conditions
by
Lim, Chae Young
,
Stein, Michael
,
Ching, Jason
,
Tang, Ruen
Published in
Environmental modelling & software : with environment data news
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Stresses in a Rotating Cylinder and Variable Thickness Disk of Anisotropic Materials
by
Tang, Ruen C.
,
Adams, Staley F.
Published in
Journal of composite materials
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Stresses in a Circular Ring with a Pressed-in Anisotropic Disc
by
Tang, Ruen C.
,
Jayne, Benjamin A.
Published in
Journal of composite materials
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Cellulose: Refutation of a Folded-Chain Structure
by
Mark, Richard E.
,
Kaloni, P. N.
,
Tang, Ruen-Chiu
,
Gillis, Peter P.
Published in
Science (American Association for the Advancement of Science)
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Surface-Based Morphometry Findings Reveal Structural Alterations of the Brain in Meige Syndrome
by
Tang, Yunyu
,
Liu, Ruen
Published in
Canadian journal of neurological sciences
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Elucidating loss-of-function mechanisms of monoallelic EPAS1 mutations underlying congenital hypoplastic anaemia in a paediatric anaemia cohort
by
Zhang, Jiasheng
,
Sun, Jin
,
Huai, Wan
,
Tang, Jie
,
Chen, Jing
,
Yao, Ruen
,
Yu, Tingting
Published in
British journal of haematology
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SINE-VNTR-Alu retrotransposon insertion as a novel mutational event underlying Glanzmann thrombasthenia
by
Zhang, Jiasheng
,
Tang, Jie
,
Li, Guoqiang
,
Li, Niu
,
Wang, Jian
,
Yao, Ruen
,
Yu, Tingting
Published in
Journal of thrombosis and haemostasis
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Genetic Diagnosis Spectrum and Multigenic Burden of Exome-Level Rare Variants in a Childhood Epilepsy Cohort
by
Yao, Ruen
,
Zhou, Yunqing
,
Tang, Jie
,
Li, Niu
,
Yu, Tingting
,
He, Yingzhong
,
Wang, Cuijin
,
Wang, Jiwen
,
Wang, Jian
Published in
Frontiers in genetics
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Assessment of Rare Genetic Variants to Identify Candidate Modifier Genes Underlying Neurological Manifestations in Neurofibromatosis 1 Patients
by
Tang, Jie
,
Li, Niu
,
Li, Guoqiang
,
Wang, Jian
,
Yu, Tingting
,
Yao, Ruen
Published in
Genes
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Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital...
by
Li, Niu
,
Xu, Yufei
,
Chen, Hongzhu
,
Lin, Jingqi
,
AlAbdi, Lama
,
Bekheirnia, Mir Reza
,
Li, Guoqiang
,
Gofin, Yoel
,
Bekheirnia, Nasim
,
Faqeih, Eissa
,
Chen, Lina
,
Chang, Guoying
,
Tang, Jie
,
Yao, Ruen
,
Yu, Tingting
,
Wang, Xiumin
,
Fu, Wei
,
Fu, Qihua
,
Shen, Yiping
,
Alkuraya, Fowzan S.
,
Machol, Keren
,
Wang, Jian
Published in
EBioMedicine
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Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital...
by
Niu Li
,
Yufei Xu
,
Hongzhu Chen
,
Jingqi Lin
,
Lama AlAbdi
,
Mir Reza Bekheirnia
,
Guoqiang Li
,
Yoel Gofin
,
Nasim Bekheirnia
,
Eissa Faqeih
,
Lina Chen
,
Guoying Chang
,
Jie Tang
,
Ruen Yao
,
Tingting Yu
,
Xiumin Wang
,
Wei Fu
,
Qihua Fu
,
Yiping Shen
,
Fowzan S. Alkuraya
,
Keren Machol
,
Jian Wang
Published in
EBioMedicine
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A Model for Predicting Risk of Serious Bacterial Infection in Febrile Infants Younger Than 3 Months of Age
by
Chen, Chun-Jen
,
Lo, Yu-Fang
,
Huang, Miao-Chiu
,
Chung, Ruey-Lung
,
Tang, Ren-Bin
,
Wu, Keh-Gong
Published in
Journal of the Chinese Medical Association
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Ebiomedicine
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