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1 . Conference
Clara: Semi-Automatic Annotation Algorithm for Medical Image Recognition
저자
by
Chen, Lijun
;
Cheng, Hanyin
;
Zhang, Yuxin
;
Xie, Xia
.
소스
2023 7th Asian Conference on Artificial Intelligence Technology (ACAIT) Artificial Intelligence Technology (ACAIT), 2023 7th Asian Conference on. :293-302 Nov, 2023
Full Text (IEEE)
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6 . Academic Journal
Establishment and Characterization of Orthotopic Mouse Models for Human Uveal Melanoma Hepatic Colonization
저자
by
Ozaki, Shinji
;
Vuyyuru, Raja
;
Kageyama, Ken
;
Terai, Mizue
;
Ohara, Masahiro
, et al.
소스
In
The American Journal of Pathology
January 2016 186(1):43-56
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7 . Academic Journal
P238: Discovery of the phenotypic landscape and mechanistic understanding of NAA10-related and NAA15-related neurodevelopmental syndromes, using mouse models and iPSCs*
저자
by
Lyon, Gholson
;
Vedaie, Marall
;
Beisheim, Travis
;
Park, Agnes
;
Marchi, Elaine
, et al.
소스
In
Genetics in Medicine Open
2023 1(1) Supplement
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7 . Academic Journal
Integrated Analyses Identify a Master MicroRNA Regulatory Network for the Mesenchymal Subtype in Serous Ovarian Cancer
저자
by
Yang, Da
;
Sun, Yan
;
Hu, Limei
;
Zheng, Hong
;
Ji, Ping
, et al.
소스
In
Cancer Cell
11 February 2013 23(2):186-199
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7 . Periodical
Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome
저자
by
Lyon, Gholson J.
;
Vedaie, Marall
;
Beisheim, Travis
;
Park, Agnes
;
Marchi, Elaine
, et al.
소스
European Journal of Human Genetics: EJHG; July 2023, Vol. 31 Issue: 7 p824-833, 10p
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7 . Academic Journal
Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity.
저자
by
Cheng, Hanyin
;
Capponi, Simona
;
Wakeling, Emma
;
Marchi, Elaine
;
Li, Quan
, et al.
소스
Human Mutation; Feb2020, Vol. 41 Issue 2, p449-464, 16p
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7 . Academic Journal
Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15.
저자
by
Cheng, Hanyin
;
Gottlieb, Leah
;
Marchi, Elaine
;
Kleyner, Robert
;
Bhardwaj, Puja
, et al.
소스
Human Molecular Genetics; 9/1/2019, Vol. 28 Issue 17, p2900-2919, 20p
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7 . Academic Journal
Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies.
저자
by
Cheng, Hanyin
;
Dharmadhikari, Avinash V.
;
Varland, Sylvia
;
Ma, Ning
;
Domingo, Deepti
, et al.
소스
American Journal of Human Genetics
. May2018, Vol. 102 Issue 5, p985-994. 10p.
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7 . Periodical
The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencing
저자
by
Feng, Yanming
;
Ge, Xiaoyan
;
Meng, Linyan
;
Scull, Jennifer
;
Li, Jianli
, et al.
소스
Genetics in Medicine; August 2017, Vol. 19 Issue: 8 p936-944, 9p
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7 . Academic Journal
Game of isoforms: PI3K β-sparing inhibitor is coming
저자
by
Cheng, Hanyin
;
Aplin, Andrew E.
.
소스
Pigment Cell & Melanoma Research
. Mar 01, 2015 28(2):133-134
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