Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 50 Records) |
Query Trace: P11[original query] |
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Genome-wide significant loci for addiction and anxiety. European psychiatry : the journal of the Association of European Psychiatrists 2016 Jun 36 47-54. Hodgson K, Almasy L, Knowles E E M, Kent J W, Curran J E, Dyer T D, Göring H H H, Olvera R L, Fox P T, Pearlson G D, Krystal J H, Duggirala R, Blangero J, Glahn D |
Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarray. Molecular cytogenetics 2016 9 16. Hu Guorui, Fan Yanjie, Wang Lili, Yao Ru-En, Huang Xiaodong, Shen Yiping, Yu Yongguo, Gu Xuef |
[Phenotypic and genetic analysis of four patients with 13q33-q34 microdeletion]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 8 34 (4): 509-513. Wang Huanhuan, Xiao Bing, Ji Xing, Zhang Jingmin, Cao Ying, Ni Lin, Ye Hui, Shen Lixi |
Myeloid/lymphoid neoplasms with FGFR1 rearrangement. Leukemia & lymphoma 2017 11 59 (7): 1672-1676. Strati Paolo, Tang Guilin, Duose Dzifa Y, Mallampati Saradhi, Luthra Rajyalakshmi, Patel Keyur P, Hussaini Mohammad, Mirza Abu-Sayeef, Komrokji Rami S, Oh Stephen, Mascarenhas John, Najfeld Vesna, Subbiah Vivek, Kantarjian Hagop, Garcia-Manero Guillermo, Verstovsek Srdan, Daver Nav |
Genetic variations in the p11/tPA/BDNF pathway are associated with post stroke depression. Journal of affective disorders 2017 Sep 226 313-325. Liang Jinfeng, Yue Yingying, Jiang Haitang, Geng Deqin, Wang Jun, Lu Jianxin, Li Shenghua, Zhang Kezhong, Wu Aiqin, Yuan Yongg |
Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH). PloS one 2018 9 13 (9): e0202576. Bibi Fehmida, Ali Isse, Naseer Muhammad Imran, Ali Mohamoud Hussein Sheikh, Yasir Muhammad, Alvi Sana Akhtar, Jiman-Fatani Asif Ahmed, Sawan Ali, Azhar Esam Ibrahe |
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients. PloS one 2018 2 13 (2): e0188869. Ji Haoran, Li Dongxiao, Wu Ye, Zhang Quanli, Gu Qiang, Xie Han, Ji Taoyun, Wang Huifang, Zhao Lu, Zhao Haijuan, Yang Yanling, Feng Hongchun, Xiong Hui, Ji Jinhua, Yang Zhixian, Kou Liping, Li Ming, Bao Xinhua, Chang Xingzhi, Zhang Yuehua, Li Li, Li Huijuan, Niu Zhengping, Wu Xiru, Xiao Jiangxi, Jiang Yuwu, Wang Jingm |
[Genetic study of a fetus with a de novo Xp22.33;Yp11.2 translocation]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 12 35 (6): 868-871. Chen Xuejiao, Dai Meizhen, Zhu Ying, He Zhehang, Zhang Yang, Pan Yihong, Shi Wei |
Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy. Frontiers in neurology 2018 12 9 947. Kessi Miriam, Xiong Juan, Wu Liwen, Yang Lifen, He Fang, Chen Chen, Pang Nan, Duan Haolin, Zhang Wen, Arafat Ahmed, Yin Fei, Peng Ji |
Pathogenic variants of DYNC2H1, KIAA0556, and PTPN11 associated with hypothalamic hamartoma. Neurology 2019 Jun . Fujita Atsushi, Higashijima Takefumi, Shirozu Hiroshi, Masuda Hiroshi, Sonoda Masaki, Tohyama Jun, Kato Mitsuhiro, Nakashima Mitsuko, Tsurusaki Yoshinori, Mitsuhashi Satomi, Mizuguchi Takeshi, Takata Atsushi, Miyatake Satoko, Miyake Noriko, Fukuda Masafumi, Kameyama Shigeki, Saitsu Hirotomo, Matsumoto Naomic |
Genetic predictor of current suicidal ideation in US service members deployed to Iraq and Afghanistan. Journal of psychiatric research 2019 3 113 65-71. Zhang Lei, Hu Xian-Zhang, Benedek David M, Fullerton Carol S, Forsten Robert D, Naifeh James A, Li Xiaoxia, |
1q23.1 homozygous deletion and downregulation of Fc receptor-like family genes confer poor prognosis in chronic lymphocytic leukemia. Clinical and experimental medicine 2019 3 19 (2): 261-267. Daniele Giulia, L'Abbate Alberto, Turchiano Antonella, Palumbo Orazio, Carella Massimo, Lo Cunsolo Crocifissa, Iuzzolino Paolo, Lonoce Angelo, Hernández-Sánchez María, Minoia Carla, Leone Patrizia, Hernandez-Rivas Jesus Maria, Storlazzi Clelia Tizia |
Acute Myeloid Leukemia with t(8;16)(p11.2;p13.3)/ KAT6A-CREBBP in a Patient with an NF1 Germline Mutation and Clinical Presentation Mimicking Acute Promyelocytic Leukemia. Journal of the Association of Genetic Technologists 2020 9 46 (3): 135-139. Donnelly Liam, Rankins Casey, Bruno Ximena Jordan, McKinnon Wendy, Devitt Katherine, Gardner Juli-An |
[Phenotypic and genetic analysis of a boy with a 10p15.3 deletion and partial trisomy 18p syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 7 37 (7): 785-788. Zhang Bo, Kong Jinghui, Mei Shiyue, Li Dongxiao, Song Yins |
[Clinical and genetic study of a child with delayed language development carrying ring 22 and a 22q13 microdeletion]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 2 37 (2): 175-177. Kong Jinghui, Zhang Bo, Ge Lili, Song Yins |
Copy neutral loss of heterozygosity (cnLOH) patterns in synchronous colorectal cancer. European journal of human genetics : EJHG 2020 Dec . Tapial Sandra, García Juan Luis, Corchete Luis, Holowatyj Andreana N, Pérez Jessica, Rueda Daniel, Urioste Miguel, González-Sarmiento Rogelio, Perea Jo |
Clinical and biological features of B-cell neoplasms with CDK6 translocations: an association with a subgroup of splenic marginal zone lymphomas displaying frequent CD5 expression, prolymphocytic cells, and TP53 abnormalities. British journal of haematology 2020 12 193 (1): 72-82. Gailllard Baptiste, Cornillet-Lefebvre Pascale, Le Quoc-Hung, Maloum Karim, Pannetier Mélanie, Lecoq-Lafon Carinne, Grange Béatrice, Jondreville Ludovic, Michaux Lucienne, Nadal Nathalie, Ittel Antoine, Luquet Isabelle, Struski Stéphanie, Lefebvre Christine, Gaillard Jean-Baptiste, Lafage-Pochitaloff Marina, Balducci Estelle, Penther Dominique, Barin Carole, Collonge-Rame Marie Agnès, Jimenez-Poquet Mélanie, Richebourg Steven, Lemaire Pierre, Defasque Sabine, Radford-Weiss Isabelle, Bidet Audrey, Susin Santos A, Nguyen-Khac Florence, Chapiro Elise, |
[Prenatal diagnosis of a fetus with chromosome 18p deletion and duplication]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 6 38 (6): 569-572. Li Wenwen, Shao Huifen, Yao Juan, Shi Chunxia, Yang Xinmiao, Zhang Jinghui, Zhang Xinli, Shen Guoso |
Copy Number Variants Captured by the Array Comparative Genomic Hybridization in a Cohort of Patients Affected with Hereditary Colorectal Cancer in Sri Lanka: The First CNV Analysis Study of the Hereditary Colorectal Cancer in the Sri Lankan Population. Asian Pacific journal of cancer prevention : APJCP 2021 6 22 (6): 1957-1966. Wijesiriwardhana Prabhavi, Wettasinghe Kalum, Dissanayeke Vajira H |
Breakpoints Identification of a Balanced Complex Chromosome Rearrangement Case: 46,XX, t(6;15;10;9)(q13;q15;p11.2;q34.3) ins(9;8)(q22.33;q21.1q21.3). Clinical laboratory 2021 4 67 (4): . Li Bohong, Li Suli, Luo Fuwei, Yang Chuanchun, Xie Jianshe |
[Molecular cytogenetic study of a case with ring chromosome 15]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 3 38 (3): 238-241. Zhang Jianlin, Yang Yimei, Zhang Junrong, Wang Shanshan, Yao Feng, Zhang Yuquan, Jiang Shengh |
Phenotypic analysis of pyrin-associated autoinflammation with neutrophilic dermatosis patients during treatment. Rheumatology (Oxford, England) 2021 3 60 (11): 5436-5446. Van Nieuwenhove Erika, De Langhe Ellen, Dooley James, Van Den Oord Joost, Shahrooei Mohammad, Parvaneh Nima, Ziaee Vahid, Savic Sinisa, Kacar Mark, Bossuyt Xavier, Humblet-Baron Stephanie, Liston Adrian, Wouters Cari |
Insertion/deletion (Indel) variant of the goat RORA gene is associated with growth traits. Animal biotechnology 2022 May 1-8. Zhou Qian, Hu Huina, Yang Yuta, Kang Yuxin, Lan Xianyong, Wu Xianfeng, Guo Zhengang, Pan Chuanyi |
Aspergillus fumigatus hijacks human p11 to redirect fungal-containing phagosomes to non-degradative pathway. Cell host & microbe 2023 3 31 (3): 373-388.e10. Jia Lei-Jie, Rafiq Muhammad, Radosa Lukáš, Hortschansky Peter, Cunha Cristina, Cseresnyés Zoltán, Krüger Thomas, Schmidt Franziska, Heinekamp Thorsten, Straßburger Maria, Löffler Bettina, Doenst Torsten, Lacerda João F, Campos António, Figge Marc Thilo, Carvalho Agostinho, Kniemeyer Olaf, Brakhage Axel |
[Genetic analysis of a Chinese pedigree with 18q21.2-q22.3 duplication and deletion in two offspring respectively resulting from a maternal intrachromosomal insertion]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 3 40 (4): 483-489. Zhou Jiahong, Zhou Pan, Lyu Zhiyu, Zhang Hui, Luo Qing, Yuan Lan, Cheng Yang, Wen Xia, Liu Jin |
Nexus between genome-wide copy number variations and autism spectrum disorder in Northeast Han Chinese population. BMC psychiatry 2023 2 23 (1): 96. Qiu Shuang, Qiu Yingjia, Li Yong, Zhu Xiaojuan, Liu Yunkai, Qiao Yichun, Cheng Yi, Liu Yaw |
[Application of copy number variation sequencing in patients with intellectual disability/developmental delay and autistic spectrum disorder]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 2 40 (3): 308-316. Lei Jie, Zhao Gang, Huang Yanke, Long Min, Li Wei, Deng Xi, Xiu Zihan, Xiao Yanwei, Zeng Sifan, Zhang Ji |
Follicular Thyroid Adenoma and Follicular Thyroid Carcinoma-A Common or Distinct Background? Loss of Heterozygosity in Comprehensive Microarray Study. Cancers 2023 2 15 (3): . Borowczyk Martyna, Dobosz Paula, Szczepanek-Parulska Ewelina, Budny Bart?omiej, D?bicki Szymon, Filipowicz Dorota, Wrotkowska El?bieta, Oszywa Michalina, Verburg Frederik A, Janicka-Jedy?ska Ma?gorzata, Ziemnicka Katarzyna, Rucha?a Mar |
Clonal hematopoiesis of a novel dic(18;20) clone following allogeneic hematopoietic stem cell transplantation. International journal of hematology 2023 11 . Makoto Ito, Nobuaki Fukushima, Tomoki Fujii, Masaya Numata, Shiori Morikawa, Yuma Kawamura, Miyo Goto, Akio Kohno, Nobuhiko Imahashi, Takahiko Yasuda, Masashi Sanada, Yuichi Ishikawa, Hitoshi Kiyoi, Kazutaka Oze |
Leukemic conversion involving RAS mutations of type 1 CALR-mutated primary myelofibrosis in a patient treated for HCV cirrhosis: a case report. Frontiers in oncology 2023 10 13 1266996. Petruta Gurban, Cristina Mambet, Anca Botezatu, Laura G Necula, Ana I Neagu, Lilia Matei, Ioana M Pitica, Saviana Nedeianu, Mihaela Chivu-Economescu, Coralia Bleotu, Marius Ataman, Gabriela Mocanu, Carmen Saguna, Anca G Pavel, Danae Stambouli, Elise Sepulchre, Gabriela Anton, Carmen C Diaconu, Stefan N Constantines |
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- Page last updated:Apr 29, 2024
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