Researcher
Sheng-Jia Lin
Oklahoma Medical Research Foundation
Statistics
22 papers found
All papers authored by Sheng-Jia Lin
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,
Sheng-Jia Lin ,
Clarissa Rocca,
Yavuz Sahin,
Aisha Al Shamsi,
Salima El Chehadeh,
Myriam Chaabouni,
Kshitij Mankad,
Evangelia Galanaki,
Stephanie Efthymiou,
Sniya Sudhakar,
Alkyoni Athanasiou-Fragkouli,
Tamer Çelik,
Nejat Narlı,
Sebastiano Bianca
and 152 other authors
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
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,
Barbara Vona ,
Hillary M. Porter ,
Mahmoud Izadi ,
Kevin Huang ,
Yves Lacassie ,
Jill A. Rosenfeld ,
Saadullah Khan ,
Cassidy Petree ,
Tayyiba A. Ali ,
Nazif Muhammad,
Sher A. Khan ,
Noor Muhammad ,
Pengfei Liu ,
Marie‐Louise Haymon
and 10 other authors
Front Cover, Volume 43, Issue 10
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,
Hannah E. Krawczyk,
Rami A. Jamra,
Sheng‐Jia Lin ,
Gökhan Yigit,
Irina Hüning,
Anna M. Polo,
Barbara Vona ,
Kevin Huang ,
Julia Schmidt,
Janine Altmüller ,
Johannes Luppe,
Konrad Platzer,
Beate B. Dörgeloh,
Andreas Busche
and 15 other authors
WARS1 and SARS1 : Two tRNA synthetases implicated in autosomal recessive microcephaly
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,
Barbara Vona ,
Hillary M. Porter ,
Mahmoud Izadi ,
Kevin Huang ,
Yves Lacassie ,
Jill A. Rosenfeld ,
Saadullah Khan ,
Cassidy Petree ,
Tayyiba A. Ali ,
Nazif Muhammad,
Sher A. Khan ,
Noor Muhammad ,
Pengfei Liu ,
Marie‐Louise Haymon
and 10 other authors
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,
Yin-Cheng Huang,
Hao-Yuan Chen,
Jia-You Fang,
Shu-Yuan Hsu,
Hung-Yu Shih,
Yu-Chien Liu,
Yi-Chuan Cheng
RGS2 Suppresses Melanoma GrowthviaInhibiting MAPK and AKT Signaling Pathways
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Barbara Vona,
Patricia G. Barbalho,
Rauan Kaiyrzhanov,
Reza Maroofian,
Cassidy Petree,
Mariasavina Severino,
Valentina Stanley,
Pratishtha Varshney,
Paulina Bahena,
Fatema Alzahrani,
Amal Alhashem,
Alistair T. Pagnamenta,
Gudrun Aubertin,
Juvianee I. Estrada-Veras
and 90 other authors
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,
Guillermo Yudowski,
Robert Kensler,
Bruno Marie,
Shawn M. Burgess,
Olivier Renaud,
Gaurav K. Varshney,
Martine Behra
Cnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors
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,
Neda Mazaheri ,
Sheng-Jia Lin ,
Lucy A. Dunbar ,
Reza Maroofian,
Hela Azaiez ,
Kevin T. Booth ,
Sandrine Vitry ,
Aboulfazl Rad ,
Franz Rüschendorf ,
Pratishtha Varshney ,
Ben Fowler,
Christian Beetz ,
Kumar N. Alagramam,
David Murphy
and 11 other authors
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
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,
Lucy A. Dunbar,
Dunbar La,
Reza Maroofian,
Kevin T. Booth,
Hela Azaiez,
Sandrine Vitry,
Pratishtha Varshney,
Booth Kt,
Aboulfazl Rad,
Christian Beetz,
Kumar N. Alagramam
and 14 other authors
Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans
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,
Hung-Yu Shih,
Chung-Han Chou,
Hsiao-Han Chu,
Ching-Chi Chiu,
Chiou-Hwa Yuh,
Tu-Hsueh Yeh,
Yi-Chuan Cheng
Epigenetic regulation of NOTCH1 and NOTCH3 by KMT2A inhibits glioma proliferation
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,
Ching-Chi Chiu,
Tsu-Lin Ma,
Tu-Hsueh Yeh,
Yi-Chuan Cheng
Download from www.researchgate.net
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