日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations

全球及特定人群中鞘氨醇磷酸裂解酶不足综合征的患病率估计

期刊:Genetics in Medicine Open
影响因子:
doi:10.1016/j.gimo.2023.100840
Sedillo, Joni C; Badduke, Chansonette; Schrodi, Steven J; Scaria, Vinod; Onat, Onur Emre; Alfadhel, Majid; Ober, Carole; Wentworth-Sheilds, William; Steiner, Robert D; Saba, Julie D
发表日期：2024
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Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis

通过临床、基因组和功能分析识别 2p15p16.1 微缺失综合征的候选基因

期刊:JCI Insight
影响因子:6.3
doi:10.1172/jci.insight.85461
Hani Bagheri, Chansonette Badduke, Ying Qiao, Rita Colnaghi, Iga Abramowicz, Diana Alcantara, Christopher Dunham, Jiadi Wen, Robert S Wildin, Malgorzata Jm Nowaczyk, Jennifer Eichmeyer, Anna Lehman, Bruno Maranda, Sally Martell, Xianghong Shan, Suzanne Me Lewis, Mark O'Driscoll, Cheryl Y Gregory-Eva
信号转导
IHC
IP
WB
发表日期：2016
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Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2

由于 2p13.2 反复微缺失导致胞外基因和视黄酸途径单倍体不足的表型和功能后果

期刊:Orphanet Journal of Rare Diseases
影响因子:3.4
doi:10.1186/1750-1172-8-100
Jiadi Wen, Fátima Lopes, Gabriela Soares, Sandra A Farrell, Cara Nelson, Ying Qiao, Sally Martell, Chansonette Badukke, Carlos Bessa, Bauke Ylstra, Suzanne Lewis, Nina Isoherranen, Patricia Maciel, Evica Rajcan-Separovic
WB
Human
EXC6B
发表日期：2013
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The expression of CXCR4, CXCL12 and CXCR7 in malignant pleural mesothelioma

CXCR4、CXCL12及CXCR7在恶性胸膜间皮瘤中的表达

期刊:Journal of Pathology
影响因子:5.6
doi:10.1002/path.2829
Tong Li, Hui Li, Yucheng Wang, Chansonette Harvard, Jia-Li Tan, Alfred Au, Zhidong Xu, David M Jablons, Liang You
肿瘤
发表日期：2011
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2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

2p15-p16.1微缺失综合征：OTX1和XPO1基因的分子特征及其与自闭症谱系障碍的关联

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2011.112
Liu, Xudong; Malenfant, Patrick; Reesor, Chelsea; Lee, Alana; Hudson, Melissa L; Harvard, Chansonette; Qiao, Ying; Persico, Antonio M; Cohen, Ira L; Chudley, Albert E; Forster-Gibson, Cynthia; Rajcan-Separovic, Evica; Lewis, M E Suzanne; Holden, Jeanette J A
OTX1
自闭症
神经科学
发表日期：2011
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Understanding the impact of 1q21.1 copy number variant

了解 1q21.1 拷贝数变异的影响

期刊:Orphanet Journal of Rare Diseases
影响因子:3.4
doi:10.1186/1750-1172-6-54
Chansonette Harvard, Emma Strong, Eloi Mercier, Rita Colnaghi, Diana Alcantara, Eva Chow, Sally Martell, Christine Tyson, Monica Hrynchak, Barbara McGillivray, Sara Hamilton, Sandra Marles, Aziz Mhanni, Angelika J Dawson, Paul Pavlidis, Ying Qiao, Jeanette J Holden, Suzanne M E Lewis, Mark O'Driscol
信号转导
WB
发表日期：2011
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Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

在非雅各布森综合征患者中发现11q24-25亚显微缺失：利用高分辨率阵列比较基因组杂交技术重新检测关键区域

期刊:Molecular Cytogenetics
影响因子:1.4
doi:10.1186/1755-8166-1-23
Tyson, Christine; Qiao, Ying; Harvard, Chansonette; Liu, Xudong; Bernier, Francois P; McGillivray, Barbara; Farrell, Sandra A; Arbour, Laura; Chudley, Albert E; Clarke, Lorne; Gibson, William; Dyack, Sarah; McLeod, Ross; Costa, Teresa; Vanallen, Margot I; Yong, Siu-Li; Graham, Gail E; Macleod, Patrick; Patel, Millan S; Hurlburt, Jane; Holden, Jeanette Ja; Lewis, Suzanne Me; Rajcan-Separovic, Evica
发表日期：2008
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