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Search Results - Heng, Julian I.‐T.
Search Results - Heng, Julian I.‐T.
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De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation
by
Haas, Matilda A.
,
Ngo, Linh
,
Li, Shan Shan
,
Schleich, Sibylle
,
Qu, Zhengdong
,
Vanyai, Hannah K.
,
Cullen, Hayley D.
,
Cardona-Alberich, Aida
,
Gladwyn-Ng, Ivan E.
,
Pagnamenta, Alistair T.
,
Taylor, Jenny C.
,
Stewart, Helen
,
Kini, Usha
,
Duncan, Kent E.
,
Teleman, Aurelio A.
,
Keays, David A.
,
Heng, Julian I.-T.
Published in
Cell reports (Cambridge)
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Understanding the impact of ZBTB18 missense variation on transcription factor function in neurodevelopment and disease
by
Heng, Julian I.‐T.
,
Viti, Leon
,
Pugh, Kye
,
Marshall, Owen J.
,
Agostino, Mark
Published in
Journal of neurochemistry
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Brain-Enriched Coding and Long Non-coding RNA Genes Are Overrepresented in Recurrent Neurodevelopmental Disorder CNVs
by
Alinejad-Rokny, Hamid
,
Heng, Julian I.T.
,
Forrest, Alistair R.R.
Published in
Cell reports (Cambridge)
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Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance
by
Woodward, Karen J.
,
Stampalia, Julie
,
Vanyai, Hannah
,
Rijhumal, Hashika
,
Potts, Kim
,
Taylor, Fiona
,
Peverall, Joanne
,
Grumball, Tanya
,
Sivamoorthy, Soruba
,
Alinejad‐Rokny, Hamid
,
Wray, John
,
Whitehouse, Andrew
,
Nagarajan, Lakshmi
,
Scurlock, Jacqueline
,
Afchani, Sabine
,
Edwards, Matthew
,
Murch, Ashleigh
,
Beilby, John
,
Baynam, Gareth
,
Kiraly‐Borri, Cathy
,
McKenzie, Fiona
,
Heng, Julian I. T.
Published in
Molecular genetics & genomic medicine
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Atypical nested 22q11.2 duplications between LCR 22B and LCR 22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance
by
Woodward, Karen J.
,
Stampalia, Julie
,
Vanyai, Hannah
,
Rijhumal, Hashika
,
Potts, Kim
,
Taylor, Fiona
,
Peverall, Joanne
,
Grumball, Tanya
,
Sivamoorthy, Soruba
,
Alinejad‐Rokny, Hamid
,
Wray, John
,
Whitehouse, Andrew
,
Nagarajan, Lakshmi
,
Scurlock, Jacqueline
,
Afchani, Sabine
,
Edwards, Matthew
,
Murch, Ashleigh
,
Beilby, John
,
Baynam, Gareth
,
Kiraly‐Borri, Cathy
,
McKenzie, Fiona
,
Heng, Julian I. T.
Published in
Molecular genetics & genomic medicine
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A novel heterozygous ZBTB18 missense mutation in a family with non-syndromic intellectual disability
by
Li, Nana
,
Kang, Hong
,
Zou, Yanna
,
Liu, Zhen
,
Deng, Ying
,
Wang, Meixian
,
Li, Lu
,
Qin, Hong
,
Qiu, Xiaoqiong
,
Wang, Yanping
,
Zhu, Jun
,
Agostino, Mark
,
Heng, Julian I-T
,
Yu, Ping
Published in
Neurogenetics
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Clinical Uncertainty in Large Vessel Occlusion ischemic stroke (CULVO): Does automated perfusion scanning make a difference? Protocol of an intrarater and interrater agreement stud...
by
Diestro, Jose Danilo Bengzon
,
Fahed, Robert
,
Benomar, Anass
,
Omar, 2nd, Abdelsimar T
,
Pereira, Vitor Mendes
,
Spears, Julian
,
Marotta, Thomas R
,
Djiadeu, Pascal
,
Sharma, Sunjay
,
Farrokhyar, Forough
Published in
PloS one
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Neurotransmitters regulate cell migration in the telencephalon
by
Heng, Julian Ik-Tsen
,
Moonen, Gustave
,
Nguyen, Laurent
Published in
The European journal of neuroscience
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