Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and FOXP1[original query] |
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| A newly identified susceptibility locus near FOXP1 modifies the association of gastroesophageal reflux with Barrett's esophagus. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015 Sep . Dai James Y, Tapsoba Jean de Dieu, Buas Matthew F, Onstad Lynn E, Levine David M, Risch Harvey A, Chow Wong-Ho, Bernstein Leslie, Ye Weimin, Lagergren Jesper, Bird Nigel C, Corley Douglas A, Shaheen Nicholas J, Wu Anna H, Reid Brian J, Hardie Laura J, Whiteman David C, Vaughan Thomas |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Rare pathogenic structural variants show potential to enhance prostate cancer germline testing for African men. Research square 2024 7 . Vanessa Hayes, Tingting Gong, Jue Jiang, Riana Bornman, Kazzem Gheybi, Phillip Stricker, Joachim Weischenfeldt, Shingai Mutambir |
| Genetic Etiology Investigation in Treatment-Resistant Nocturnal Enuresis Children: A descriptive study. Urology journal 2024 12 . Sevim Yener, Metin Es |
| Copy Number Variants in 30 Saudi Pediatric Patients with Neurodevelopmental Disorders: From Unknown Significance to Diagnosis. Saudi journal of medicine & medical sciences 2024 11 12 (4): 292-298. Raniah Saleem Alotibi, Mariam M Al Eissa, Taghrid Aloraini, Khalidah Khalid Nasser, Muneera J Al Shammari, Amerh S Alqahta |
- Page last reviewed:Feb 1, 2024
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