Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 47 Records) |
Query Trace: EBF1[original query] |
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Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Nature genetics 2017 Jan 49 (1): 125-130. Chu Audrey Y, Deng Xuan, Fisher Virginia A, Drong Alexander, Zhang Yang, Feitosa Mary F, Liu Ching-Ti, Weeks Olivia, Choh Audrey C, Duan Qing, Dyer Thomas D, Eicher John D, Guo Xiuqing, Heard-Costa Nancy L, Kacprowski Tim, Kent Jack W, Lange Leslie A, Liu Xinggang, Lohman Kurt, Lu Lingyi, Mahajan Anubha, O'Connell Jeffrey R, Parihar Ankita, Peralta Juan M, Smith Albert V, Zhang Yi, Homuth Georg, Kissebah Ahmed H, Kullberg Joel, Laqua René, Launer Lenore J, Nauck Matthias, Olivier Michael, Peyser Patricia A, Terry James G, Wojczynski Mary K, Yao Jie, Bielak Lawrence F, Blangero John, Borecki Ingrid B, Bowden Donald W, Carr John Jeffrey, Czerwinski Stefan A, Ding Jingzhong, Friedrich Nele, Gudnason Vilmunder, Harris Tamara B, Ingelsson Erik, Johnson Andrew D, Kardia Sharon L R, Langefeld Carl D, Lind Lars, Liu Yongmei, Mitchell Braxton D, Morris Andrew P, Mosley Thomas H, Rotter Jerome I, Shuldiner Alan R, Towne Bradford, Völzke Henry, Wallaschofski Henri, Wilson James G, Allison Matthew, Lindgren Cecilia M, Goessling Wolfram, Cupples L Adrienne, Steinhauser Matthew L, Fox Caroline |
Genome-wide Association Study of Parental Life Span.
The journals of gerontology. Series A, Biological sciences and medical sciences 2016 Nov . Tanaka Toshiko, Dutta Ambarish, Pilling Luke C, Xue Luting, Lunetta Kathryn L, Murabito Joanne M, Bandinelli Stefania, Wallace Robert, Melzer David, Ferrucci Lui |
The correlation between Pax5 deletion and patients survival in Iranian children with precursor B-cell acute lymphocytic leukemia. Cellular and molecular biology (Noisy-le-Grand, France) 2017 9 63 (8): 19-22. Moafi A, Zojaji A, Salehi R, Najafi Dorcheh S, Rahgozar |
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
The New England journal of medicine 2017 Sep . Zhang Ge, Feenstra Bjarke, Bacelis Jonas, Liu Xueping, Muglia Lisa M, Juodakis Julius, Miller Daniel E, Litterman Nadia, Jiang Pan-Pan, Russell Laura, Hinds David A, Hu Youna, Weirauch Matthew T, Chen Xiaoting, Chavan Arun R, Wagner Günter P, Pavli?ev Mihaela, Nnamani Mauris C, Maziarz Jamie, Karjalainen Minna K, Rämet Mika, Sengpiel Verena, Geller Frank, Boyd Heather A, Palotie Aarno, Momany Allison, Bedell Bruce, Ryckman Kelli K, Huusko Johanna M, Forney Carmy R, Kottyan Leah C, Hallman Mikko, Teramo Kari, Nohr Ellen A, Davey Smith George, Melbye Mads, Jacobsson Bo, Muglia Louis |
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.
Scientific reports 2017 Jun 7 (1): 3847. Li Dong, Chang Xiao, Connolly John J, Tian Lifeng, Liu Yichuan, Bhoj Elizabeth J, Robinson Nora, Abrams Debra, Li Yun R, Bradfield Jonathan P, Kim Cecilia E, Li Jin, Wang Fengxiang, Snyder James, Lemma Maria, Hou Cuiping, Wei Zhi, Guo Yiran, Qiu Haijun, Mentch Frank D, Thomas Kelly A, Chiavacci Rosetta M, Cone Roger, Li Bingshan, Sleiman Patrick A, , , Hakonarson Hak |
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients. Genes, chromosomes & cancer 2017 Jun . Busse Tracy M, Roth Jacquelyn J, Wilmoth Donna, Wainwright Luanne, Tooke Laura, Biegel Jaclyn |
Clinical significance of recurrent copy number aberrations in B-lineage acute lymphoblastic leukaemia without recurrent fusion genes across age cohorts. British journal of haematology 2017 Apr . Messina Monica, Chiaretti Sabina, Fedullo Anna Lucia, Piciocchi Alfonso, Puzzolo Maria Cristina, Lauretti Alessia, Gianfelici Valentina, Apicella Valerio, Fazi Paola, Te Kronnie Geertruy, Testi Anna Maria, Vitale Antonella, Guarini Anna, Foà Rob |
Correlates of Prenatal and Early-Life Tobacco Smoke Exposure and Frequency of Common Gene Deletions in Childhood Acute Lymphoblastic Leukemia. Cancer research 2017 04 77 (7): 1674-1683. de Smith Adam J, Kaur Maneet, Gonseth Semira, Endicott Alyson, Selvin Steve, Zhang Luoping, Roy Ritu, Shao Xiaorong, Hansen Helen M, Kang Alice Y, Walsh Kyle M, Dahl Gary V, McKean-Cowdin Roberta, Metayer Catherine, Wiemels Joseph |
Genomic analysis of adult B-ALL identifies potential markers of shorter survival. Leukemia research 2017 Feb 56 44-51. Patel Shiven, Mason Clinton C, Glenn Martha J, Paxton Christian N, South Sara T, Cessna Melissa H, Asch Julie, Cobain Erin F, Bixby Dale L, Smith Lauren B, Reshmi Shalini, Gastier-Foster Julie M, Schiffman Joshua D, Miles Rodney |
Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease. BMC cardiovascular disorders 2017 Feb 17 (1): 57. Li Yafei, Xie Zhiyong, Chen Lei, Yan Jianjun, Ma Yao, Wang Liansheng, Chen Zho |
Association of genetic variation with blood pressure traits among East Africans. Clinical genetics 2017 Jan . Kayima James, Liang Jingjing, Natanzon Yanina, Nankabirwa Joaniter, Ssinabulya Isaac, Nakibuuka Jane, Katamba Achilles, Mayanja-Kizza Harriet, Miron Alexander, Li Chun, Zhu Xiaofe |
EBF1 gene polymorphism and its interaction with smoking and drinking on the risk of coronary artery disease for Chinese patients. Bioscience reports 2018 May . Ying Yongjun, Luo Yuxuan, Peng H |
Simultaneous detection of ABL1 mutation and IKZF1 deletion in Philadelphia chromosome-positive acute lymphoblastic leukemia using a customized target enrichment system panel. International journal of laboratory hematology 2018 Mar . Aoe M, Ishida H, Matsubara T, Karakawa S, Kawaguchi H, Fujiwara K, Kanamitsu K, Washio K, Okada K, Shibakura M, Shimada |
Prognostic significance of copy number alterations detected by multi-link probe amplification of multiple genes in adult acute lymphoblastic leukemia. Oncology letters 2018 Apr 15 (4): 5359-5367. Fang Qiuyun, Yuan Tian, Li Yan, Feng Juan, Gong Xiaoyuan, Li Qinghua, Zhao Xingli, Liu Kaiqi, Tang Kejing, Tian Zheng, Zhang Qi, Wang Ying, Liu Bingcheng, Wang Min, Ru Kun, Wang Jianxiang, Mi Yingcha |
High frequency of intermediate and poor risk copy number abnormalities in pediatric cohort of B-ALL correlate with high MRD post induction. Leukemia research 2018 2 66 79-84. Singh Minu, Bhatia Prateek, Trehan Amita, Varma Neelam, Sachdeva Manupdesh Singh, Bansal Deepak, Jain Richa, Naseem Sha |
Genome-wide association study of offspring birth weight in 86?577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.
Human molecular genetics 2018 Feb 27 (4): 742-756. Beaumont Robin N, Warrington Nicole M, Cavadino Alana, Tyrrell Jessica, Nodzenski Michael, Horikoshi Momoko, Geller Frank, Myhre Ronny, Richmond Rebecca C, Paternoster Lavinia, Bradfield Jonathan P, Kreiner-Møller Eskil, Huikari Ville, Metrustry Sarah, Lunetta Kathryn L, Painter Jodie N, Hottenga Jouke-Jan, Allard Catherine, Barton Sheila J, Espinosa Ana, Marsh Julie A, Potter Catherine, Zhang Ge, Ang Wei, Berry Diane J, Bouchard Luigi, Das Shikta, , Hakonarson Hakon, Heikkinen Jani, Helgeland Øyvind, Hocher Berthold, Hofman Albert, Inskip Hazel M, Jones Samuel E, Kogevinas Manolis, Lind Penelope A, Marullo Letizia, Medland Sarah E, Murray Anna, Murray Jeffrey C, Njølstad Pål R, Nohr Ellen A, Reichetzeder Christoph, Ring Susan M, Ruth Katherine S, Santa-Marina Loreto, Scholtens Denise M, Sebert Sylvain, Sengpiel Verena, Tuke Marcus A, Vaudel Marc, Weedon Michael N, Willemsen Gonneke, Wood Andrew R, Yaghootkar Hanieh, Muglia Louis J, Bartels Meike, Relton Caroline L, Pennell Craig E, Chatzi Leda, Estivill Xavier, Holloway John W, Boomsma Dorret I, Montgomery Grant W, Murabito Joanne M, Spector Tim D, Power Christine, Järvelin Marjo-Ritta, Bisgaard Hans, Grant Struan F A, Sørensen Thorkild I A, Jaddoe Vincent W, Jacobsson Bo, Melbye Mads, McCarthy Mark I, Hattersley Andrew T, Hayes M Geoffrey, Frayling Timothy M, Hivert Marie-France, Felix Janine F, Hyppönen Elina, Lowe William L, Evans David M, Lawlor Debbie A, Feenstra Bjarke, Freathy Rachel |
Genomic CDKN2A/2B deletions in adult Ph ALL are adverse despite allogeneic stem cell transplantation. Blood 2018 Jan . Pfeifer Heike, Raum Katharina, Markovic Sandra, Nowak Verena, Fey Stephanie, Obländer Julia, Pressler Jovita, Böhm Verena, Brüggemann Monika, Wunderle Lydia, Hüttmann Andreas, Wäsch Ralph, Beck Joachim, Stelljes Matthias, Viardot Andreas, Lang Fabian, Hoelzer Dieter, Hofmann Wolf-Karsten, Serve Hubert, Weiss Christel, Goekbuget Nicola, Ottmann Oliver G, Nowak Dani |
Varicose veins of lower extremities: Insights from the first large-scale genetic study.
PLoS genetics 2019 Apr 15 (4): e1008110. Shadrina Alexandra S, Sharapov Sodbo Z, Shashkova Tatiana I, Tsepilov Yakov |
Potential Markers of Autoimmune Diseases, Alleles rs115662534(T) and rs548231435(C), Disrupt the Binding of Transcription Factors STAT1 and EBF1 to the Regulatory Elements of Human CD40 Gene. Biochemistry. Biokhimiia 2019 3 83 (12): 1534-1542. Putlyaeva L V, Demin D E, Korneev K V, Kasyanov A S, Tatosyan K A, Kulakovskiy I V, Kuprash D V, Schwartz A |
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.
eLife 2019 01 8 . Timmers Paul Rhj, Mounier Ninon, Lall Kristi, Fischer Krista, Ning Zheng, Feng Xiao, Bretherick Andrew D, Clark David W, , Shen Xia, Esko Tõnu, Kutalik Zoltán, Wilson James F, Joshi Peter |
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia. Scientific reports 2020 Jul 10 (1): 11501. Yu Chih-Hsiang, Lin Tze-Kang, Jou Shiann-Tarng, Lin Chien-Yu, Lin Kai-Hsin, Lu Meng-Yao, Chen Shu-Huey, Cheng Chao-Neng, Wu Kang-Hsi, Wang Shih-Chung, Chang Hsiu-Hao, Li Meng-Ju, Ni Yu-Ling, Su Yi-Ning, Lin Dong-Tsamn, Chen Hsuan-Yu, Harrison Christine J, Hung Chia-Cheng, Lin Shu-Wha, Yang Yung- |
Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol. Genes, chromosomes & cancer 2020 6 59 (11): 667-671. Jung Mareike, Schieck Maximilian, Hofmann Winfried, Tauscher Marcel, Lentes Jana, Bergmann Anke, Stelter Marie, Möricke Anja, Alten Julia, Schlegelberger Brigitte, Schrappe Martin, Zimmermann Martin, Stanulla Martin, Cario Gunnar, Steinemann Dor |
Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms.
Annals of the rheumatic diseases 2020 Oct . López-Isac Elena, Smith Samantha L, Marion Miranda C, Wood Abigail, Sudman Marc, Yarwood Annie, Shi Chenfu, Gaddi Vasanthi Priyadarshini, Martin Paul, Prahalad Sampath, Eyre Stephen, Orozco Gisela, Morris Andrew P, Langefeld Carl D, Thompson Susan D, Thomson Wendy, Bowes Jo |
Evaluating the precision of EBF1 SNP x stress interaction association: sex, race, and age differences in a big harmonized data set of 28,026 participants. Translational psychiatry 2020 10 10 (1): 351. Singh Abanish, Babyak Michael A, Sims Mario, Musani Solomon K, Brummett Beverly H, Jiang Rong, Kraus William E, Shah Svati H, Siegler Ilene C, Hauser Elizabeth R, Williams Redford |
Genetic profile and immunohistochemical study of clear cell renal carcinoma: Pathological-anatomical correlation and prognosis. Cancer treatment and research communications 2021 5 27 100374. Diez-Calzadilla N A, Noguera Salvá R, Soriano Sarrió P, Martínez-Jabaloyas J |
Philadelphia chromosome-negative B-cell acute lymphoblastic leukaemia with kinase fusions in Taiwan. Scientific reports 2021 3 11 (1): 5802. Hsu Yin-Chen, Yu Chih-Hsiang, Chen Yan-Ming, Roberts Kathryn G, Ni Yu-Ling, Lin Kai-Hsin, Jou Shiann-Tarng, Lu Meng-Yao, Chen Shu-Huey, Wu Kang-Hsi, Chang Hsiu-Hao, Lin Dong-Tsamn, Lin Shu-Wha, Lin Ze-Shiang, Chiu Wei-Tzu, Chang Chia-Ching, Ho Bing-Ching, Mullighan Charles G, Yu Sung-Liang, Yang Yung- |
Biomarkers of response to ibrutinib plus nivolumab in relapsed diffuse large B-cell lymphoma, follicular lymphoma, or Richter's transformation. Translational oncology 2021 1 14 (1): 100977. Hodkinson Brendan P, Schaffer Michael, Brody Joshua D, Jurczak Wojciech, Carpio Cecilia, Ben-Yehuda Dina, Avivi Irit, Forslund Ann, Özcan Muhit, Alvarez John, Ceulemans Rob, Fourneau Nele, Younes Anas, Balasubramanian Srir |
Copy Number Alteration Profile Provides Additional Prognostic Value for Acute Lymphoblastic Leukemia Patients Treated on BFM Protocols. Cancers 2021 Jun 13 (13): . Αmpatzidou Μirella, Florentin Lina, Papadakis Vassilios, Paterakis Georgios, Tzanoudaki Marianna, Bouzarelou Dimitra, Papadhimitriou Stefanos I, Polychronopoulou Soph |
Caveolin-1 rs1997623 Single Nucleotide Polymorphism Creates a New Binding Site for the Early B-Cell Factor 1 That Instigates Adipose Tissue CAV1 Protein Overexpression. Cells 2022 12 11 (23): . Al Madhoun Ashraf, Haddad Dania, Nizam Rasheeba, Miranda Lavina, Kochumon Shihab, Thomas Reeby, Thanaraj Thangavel Alphonse, Ahmad Rasheed, Bitar Milad S, Al-Mulla Fa |
Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications.
Genes 2022 12 13 (12): . Changalidis Anton I, Maksiutenko Evgeniia M, Barbitoff Yury A, Tkachenko Alexander A, Vashukova Elena S, Pachuliia Olga V, Nasykhova Yulia A, Glotov Andrey |
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- Page last updated:Apr 22, 2024
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