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American Journal on Intellectual and Developmental Disabilities
|
November 14, 2018
Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project
Tracie C Rosser, Jamie O Edgin, George T Capone, et al.
Nature Neuroscience
|
August 20, 2021
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Yunhee Kang, Ying Zhou, Yujing Li, et al.
Science Advances
|
November 23, 2022
Expression of expanded GGC repeats within <i>NOTCH2NLC</i> causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Genome Biology
|
April 30, 2021
Ten-eleven translocation protein 1 modulates medulloblastoma progression
Hyerim Kim, Yunhee Kang, Yujing Li, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome
Ha Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Nature Communications
|
July 8, 2025
Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome
Zhenhua Li, Wenjian Yang, Gang Wu, et al.
Fertility and Sterility
|
May 21, 2021
Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation
Cristina E Trevino, J Christopher Rounds, Krista Charen, et al.
American Journal of Human Genetics
|
June 17, 2026
Complete chromosome 21 centromere sequencing of families with Down syndrome
F Kumara Mastrorosa, Alessia Daponte, Luciana de Gennaro, et al.
American Journal of Human Genetics
|
June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders
Yun Tian, Jun-Ling Wang, Wen Huang, et al.
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of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
American Journal on Intellectual and Developmental Disabilities
|
November 14, 2018
Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project
Tracie C Rosser, Jamie O Edgin, George T Capone, et al.
Nature Neuroscience
|
August 20, 2021
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Yunhee Kang, Ying Zhou, Yujing Li, et al.
Science Advances
|
November 23, 2022
Expression of expanded GGC repeats within <i>NOTCH2NLC</i> causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Genome Biology
|
April 30, 2021
Ten-eleven translocation protein 1 modulates medulloblastoma progression
Hyerim Kim, Yunhee Kang, Yujing Li, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome
Ha Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Nature Communications
|
July 8, 2025
Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome
Zhenhua Li, Wenjian Yang, Gang Wu, et al.
Fertility and Sterility
|
May 21, 2021
Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation
Cristina E Trevino, J Christopher Rounds, Krista Charen, et al.
American Journal of Human Genetics
|
June 17, 2026
Complete chromosome 21 centromere sequencing of families with Down syndrome
F Kumara Mastrorosa, Alessia Daponte, Luciana de Gennaro, et al.
American Journal of Human Genetics
|
June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders
Yun Tian, Jun-Ling Wang, Wen Huang, et al.
Page
of 6