Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 45 Records) |
Query Trace: FOXP1[original query] |
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Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits. Scientific reports 2016 6 32894. Bakshi Andrew, Zhu Zhihong, Vinkhuyzen Anna A E, Hill W David, McRae Allan F, Visscher Peter M, Yang Ji |
Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep . Bekheirnia Mir Reza, Bekheirnia Nasim, Bainbridge Matthew N, Gu Shen, Coban Akdemir Zeynep Hande, Gambin Tomek, Janzen Nicolette K, Jhangiani Shalini N, Muzny Donna M, Michael Mini, Brewer Eileen D, Elenberg Ewa, Kale Arundhati S, Riley Alyssa A, Swartz Sarah J, Scott Daryl A, Yang Yaping, Srivaths Poyyapakkam R, Wenderfer Scott E, Bodurtha Joann, Applegate Carolyn D, Velinov Milen, Myers Angela, Borovik Lior, Craigen William J, Hanchard Neil A, Rosenfeld Jill A, Lewis Richard Alan, Gonzales Edmond T, Gibbs Richard A, Belmont John W, Roth David R, Eng Christine, Braun Michael C, Lupski James R, Lamb Dolores |
Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma.
The Journal of investigative dermatology 2016 Jan . Asgari Maryam M, Wang Wei, Ioannidis Nilah M, Itnyre Jacqueline, Hoffmann Thomas, Jorgenson Eric, Whittemore Alice |
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Molecular autism 2017 8 21. Authors are not available |
FOXP1 expression is a prognostic biomarker in follicular lymphoma treated with rituximab and chemotherapy. Blood 2017 11 131 (2): 226-235. Mottok Anja, Jurinovic Vindi, Farinha Pedro, Rosenwald Andreas, Leich Ellen, Ott German, Horn Heike, Klapper Wolfram, Boesl Michael, Hiddemann Wolfgang, Steidl Christian, Connors Joseph M, Sehn Laurie H, Gascoyne Randy D, Hoster Eva, Weigert Oliver, Kridel Robe |
Influence of Genetic Polymorphism Towards Pulmonary Tuberculosis Susceptibility. Frontiers in medicine 2018 5 213. Harishankar Murugesan, Selvaraj Paramasivam, Bethunaickan Ramaling |
Genetic variants of FOXP1 and FOXF1 are associated with the susceptibility of oesophageal adenocarcinoma in Chinese population. Journal of genetics 2018 Mar 97 (1): 213-218. Zhang Jie, Chen Jiebin, Ma Tianheng, Guo Huimin, Yang B |
Prognostic impact of kinase-activating fusions and IKZF1 deletions in pediatric high-risk B-lineage acute lymphoblastic leukemia. Blood advances 2018 Mar 2 (5): 529-533. Tran Thai Hoa, Harris Marian H, Nguyen Jonathan V, Blonquist Traci M, Stevenson Kristen E, Stonerock Eileen, Asselin Barbara L, Athale Uma H, Clavell Luis A, Cole Peter D, Kelly Kara M, Laverdiere Caroline, Leclerc Jean-Marie, Michon Bruno, Schorin Marshall A, Welch Jennifer J G, Reshmi Shalini C, Neuberg Donna S, Sallan Stephen E, Loh Mignon L, Silverman Lewis |
SNP-array lesions in core binding factor acute myeloid leukemia. Oncotarget 2018 Jan 9 (5): 6478-6489. Duployez Nicolas, Boudry-Labis Elise, Roumier Christophe, Boissel Nicolas, Petit Arnaud, Geffroy Sandrine, Helevaut Nathalie, Celli-Lebras Karine, Terré Christine, Fenneteau Odile, Cuccuini Wendy, Luquet Isabelle, Lapillonne Hélène, Lacombe Catherine, Cornillet Pascale, Ifrah Norbert, Dombret Hervé, Leverger Guy, Jourdan Eric, Preudhomme Clau |
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts. American journal of medical genetics. Part A 2019 Mar 179 (3): 467-474. Shaffer John R, LeClair Jessica, Carlson Jenna C, Feingold Eleanor, Buxó Carmen J, Christensen Kaare, Deleyiannis Frederic W B, Field L Leigh, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Murray Jeffrey C, Weinberg Seth M, Marazita Mary L, Leslie Elizabeth |
Three Japanese patients with 3p13 microdeletions involving FOXP1. Brain & development 2018 11 41 (3): 257-262. Yamamoto-Shimojima Keiko, Okamoto Nobuhiko, Matsumura Wataru, Okazaki Tetsuya, Yamamoto Toshiyu |
Identification of prognostic molecular biomarkers in 157 HPV-positive and HPV-negative squamous cell carcinomas of the oropharynx. International journal of cancer 2019 5 145 (11): 3152-3162. Dogan Snjezana, Xu Bin, Middha Sumit, Vanderbilt Chad M, Bowman Anita S, Migliacci Jocelyn, Morris Luc G T, Seshan Venkatraman E, Ganly I |
De novo damaging variants associated with congenital heart diseases contribute to the connectome. Scientific reports 2020 Apr 10 (1): 7046. Ji Weizhen, Ferdman Dina, Copel Joshua, Scheinost Dustin, Shabanova Veronika, Brueckner Martina, Khokha Mustafa K, Ment Laura |
Genomic influences on self-reported childhood maltreatment.
Translational psychiatry 2020 Jan 10 (1): 38. Dalvie Shareefa, Maihofer Adam X, Coleman Jonathan R I, Bradley Bekh, Breen Gerome, Brick Leslie A, Chen Chia-Yen, Choi Karmel W, Duncan Laramie E, Guffanti Guia, Haas Magali, Harnal Supriya, Liberzon Israel, Nugent Nicole R, Provost Allison C, Ressler Kerry J, Torres Katy, Amstadter Ananda B, Bryn Austin S, Baker Dewleen G, Bolger Elizabeth A, Bryant Richard A, Calabrese Joseph R, Delahanty Douglas L, Farrer Lindsay A, Feeny Norah C, Flory Janine D, Forbes David, Galea Sandro, Gautam Aarti, Gelernter Joel, Hammamieh Rasha, Jett Marti, Junglen Angela G, Kaufman Milissa L, Kessler Ronald C, Khan Alaptagin, Kranzler Henry R, Lebois Lauren A M, Marmar Charles, Mavissakalian Matig R, McFarlane Alexander, Donnell Meaghan O', Orcutt Holly K, Pietrzak Robert H, Risbrough Victoria B, Roberts Andrea L, Rothbaum Alex O, Roy-Byrne Peter, Ruggiero Ken, Seligowski Antonia V, Sheerin Christina M, Silove Derrick, Smoller Jordan W, Stein Murray B, Teicher Martin H, Ursano Robert J, Van Hooff Miranda, Winternitz Sherry, Wolff Jonathan D, Yehuda Rachel, Zhao Hongyu, Zoellner Lori A, Stein Dan J, Koenen Karestan C, Nievergelt Caroline |
Systematic analyses of genetic variants in chromatin interaction regions identified four novel lung cancer susceptibility loci. Journal of Cancer 2020 11 (5): 1075-1081. Ji Pei, Ding Dongsheng, Qin Na, Wang Cheng, Zhu Meng, Li Yuancheng, Dai Juncheng, Jin Guangfu, Hu Zhibin, Shen Hongbing, Chen Liang, Ma Hongx |
MN1, FOXP1 and hsa-miR-181a-5p as prognostic markers in acute myeloid leukemia patients treated with intensive induction chemotherapy and autologous stem cell transplantation. Leukemia research 2020 1 89 106296. Seipel Katja, Messerli Christian, Wiedemann Gertrud, Bacher Ulrike, Pabst Thom |
Genetic heterogeneity of disorders with overgrowth and intellectual disability: Experience from a center in North India. American journal of medical genetics. Part A 2021 5 185 (8): 2345-2355. Moirangthem Amita, Mandal Kausik, Saxena Deepti, Srivastava Priyanka, Gambhir Poonam Singh, Agrawal Neha, Shambhavi Arya, Nampoothiri Sheela, Phadke Shubha |
Investigation of Association of Rare, Functional Genetic Variants With Heavy Drinking and Problem Drinking in Exome Sequenced UK Biobank Participants. Alcohol and alcoholism (Oxford, Oxfordshire) 2021 Apr . Curtis Dav |
Impact of FOXP1 rs2687201 genetic variant on the susceptibility to HCV-related hepatocellular carcinoma in Egyptians. Journal of biochemical and molecular toxicology 2021 Nov e22965. Motawi Tarek Mohamed Kamal, Sabry Dina, Shehata Nagwa Ibrahim, William Mira Magdy, Fahim Atef Tadr |
Endometrial Cancer in Aspect of Forkhead Box Protein Contribution. International journal of environmental research and public health 2022 8 19 (16): . Adamczyk-Gruszka Olga, Horecka-Lewitowicz Agata, Gruszka Jakub, Wawszczak-Kasza Monika, Strzelecka Agnieszka, Lewitowicz Pio |
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes. Nature genetics 2022 Sep 54 (9): 1305-1319. Zhou Xueya, Feliciano Pamela, Shu Chang, Wang Tianyun, Astrovskaya Irina, Hall Jacob B, Obiajulu Joseph U, Wright Jessica R, Murali Shwetha C, Xu Simon Xuming, Brueggeman Leo, Thomas Taylor R, Marchenko Olena, Fleisch Christopher, Barns Sarah D, Snyder LeeAnne Green, Han Bing, Chang Timothy S, Turner Tychele N, Harvey William T, Nishida Andrew, O'Roak Brian J, Geschwind Daniel H, , Michaelson Jacob J, Volfovsky Natalia, Eichler Evan E, Shen Yufeng, Chung Wendy |
Single nucleotide polymorphisms in FOXP1 and RORA of the lymphocyte activation-related pathway affect survival of lung cancer patients. Translational lung cancer research 2022 May 11 (5): 890-901. Du Hailei, Mu Rui, Liu Lihua, Liu Hongliang, Luo Sheng, Patz Edward F, Glass Carolyn, Su Li, Du Mulong, Christiani David C, Li Hecheng, Wei Qing |
Screening for modulators of autism spectrum disorder using induced human neurons. SLAS discovery : advancing life sciences R & D 2022 2 27 (2): 128-139. Rao Sumitha Rajendra, Kostic Ana, Baillargeon Pierre, Fernandez-Vega Virneliz, de Anda Mitzy Rios, Fletcher Kelty, Shumate Justin, Scampavia Louis, Buxbaum Joseph D, Spicer Timothy |
Exome Evaluation of Autism-Associated Genes in Amazon American Populations. Genes 2022 2 13 (2): . da Costa Giovana E, Fernandes Giordane L, Rodrigues Juliana C G, da V B Leal Diana F, Pastana Lucas F, Pereira Esdras E B, Assumpção Paulo P, Burbano Rommel M R, Dos Santos Sidney E B, Guerreiro João F, Fernandes Marianne R, Dos Santos Ney P |
The FoxP1 gene regulates lung function, production of matrix metalloproteinases and inflammatory mediators, and viability of lung epithelia. Respiratory research 2022 Oct 23 (1): 281. Andreas Alexis, Maloy Abby, Nyunoya Toru, Zhang Yingze, Chandra Div |
Analysis of a large prostate cancer family identifies novel and recurrent gene fusion events providing evidence for inherited predisposition. The Prostate 2022 1 82 (5): 540-550. Raspin Kelsie, O'Malley Dannielle E, Marthick James R, Donovan Shaun, Malley Roslyn C, Banks Annette, Redwig Frank, Skala Marketa, Dickinson Joanne L, FitzGerald Liesel |
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention. Genes 2021 12 13 (1): . Fernàndez-Castillo Noèlia, Cabana-Domínguez Judit, Kappel Djenifer B, Torrico Bàrbara, Weber Heike, Lesch Klaus-Peter, Lao Oscar, Reif Andreas, Cormand B |
Construction of a risk stratification model integrating ctDNA to predict response and survival in neoadjuvant-treated breast cancer. BMC medicine 2023 12 21 (1): 493. Zhaoyun Liu, Bo Yu, Mu Su, Chenxi Yuan, Cuicui Liu, Xinzhao Wang, Xiang Song, Chao Li, Fukai Wang, Jianli Ma, Meng Wu, Dawei Chen, Jinming Yu, Zhiyong |
Exome-wide analysis implicates rare protein-altering variants in human handedness. Nature communications 2024 4 15 (1): 2632. Dick Schijven, Sourena Soheili-Nezhad, Simon E Fisher, Clyde Franc |
Genomic and transcriptomic analysis of breast cancer identifies novel signatures associated with response to neoadjuvant chemotherapy. Genome medicine 2024 1 16 (1): 11. Gengshen Yin, Liyuan Liu, Ting Yu, Lixiang Yu, Man Feng, Chengjun Zhou, Xiaoying Wang, Guoxin Teng, Zhongbing Ma, Wenzhong Zhou, Chunmiao Ye, Jialin Zhang, Changhua Ji, Linfeng Zhao, Peng Zhou, Yaxun Guo, Xingchen Meng, Qinye Fu, Qiang Zhang, Liang Li, Fei Zhou, Chao Zheng, Yujuan Xiang, Mingming Guo, Yongjiu Wang, Fei Wang, Shuya Huang, Zhigang |
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- Page last updated:Apr 22, 2024
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