HuGE Literature Finder
Records 1-30
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Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis.
Pediatric research 2020 May . Zysman-Colman Zofia N, Kilberg Marissa J, Harrison Victor S, Chesi Alessandra, Grant Struan F A, Mitchell Jonathan, Sheikh Saba, Hadjiliadis Denis, Rickels Michael R, Rubenstein Ronald C, Kelly Andr |
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Intranasal perillyl alcohol therapy improves survival of patients with recurrent glioblastoma harboring mutant variant for MTHFR rs1801133 polymorphism.
BMC cancer 2020 Apr 20 (1): 294. Faria Giselle M, Soares Igor D P, D'Alincourt Salazar Marcela, Amorim Marcia R, Pessoa Bruno L, da Fonseca Clovis O, Quirico-Santos There |
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Common variation in FAM155A is associated with diverticulitis but not diverticulosis.
Scientific reports 2020 Feb 10 (1): 1658. Reichert Matthias C, Kupcinskas Juozas, Schulz Antje, Schramm Christoph, Weber Susanne N, Krawczyk Marcin, Jüngst Christoph, Casper Markus, Grünhage Frank, Appenrodt Beate, Zimmer Vincent, Tamelis Algimantas, Lukosiene Jaune I, Pauziene Neringa, Kiudelis Gediminas, Jonaitis Laimas, Goeser Tobias, Malinowski Maciej, Glanemann Matthias, Kupcinskas Limas, Lammert Fra |
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Immunomodulatory function of the cystic fibrosis modifier gene BPIFA1.
PloS one 2020 15 (1): e0227067. Saferali Aabida, Tang Anthony C, Strug Lisa J, Quon Bradley S, Zlosnik James, Sandford Andrew J, Turvey Stuart |
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Next-generation sequencing identified somatic alterations that may underlie the etiology of Chinese papillary thyroid carcinoma.
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2019 Nov . Yang Chuanjia, Gong Jian, Xu Weixue, Liu Zhen, Cui Dong |
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The effect of genetic and nongenetic factors on warfarin dose variability in Qatari population.
The pharmacogenomics journal 2019 Oct . Bader Loulia, Mahfouz Ahmad, Kasem Mohammed, Mohammed Shaban, Alsaadi Sumayya, Abdelsamad Osama, Elenani Rasha, Soaly Ezeldin, Elzouki Abdelnasser, Rizk Nasser, Khalifa Sherief, Shahin Mohamed H, Cavallari Larisa H, Mraiche Fatima, Elewa Haz |
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TNFA -308G>A and -238G>A polymorphisms and risk to systemic sclerosis: impact on TNF-a serum levels, TNFA mRNA expression, and autoantibodies.
Clinical and experimental medicine 2019 Jul . Lomelí-Nieto José Alvaro, Muñoz-Valle José Francisco, Baños-Hernández Christian Johana, Navarro-Zarza José Eduardo, Ramírez-Dueñas María Guadalupe, Sánchez-Hernández Pedro Ernesto, Machado-Sulbaran Andrea Carolina, Parra-Rojas Isela, García-Chagollán Mariel, Hernández-Bello Jor |
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Association of Folate and Vitamins Involved in the 1-Carbon Cycle with Polymorphisms in the Methylenetetrahydrofolate Reductase Gene (MTHFR) and Global DNA Methylation in Patients with Colorectal Cancer.
Nutrients 2019 Jun 11 (6): . Ferrari Ariana, Torrezan Giovana Tardin, Carraro Dirce Maria, Aguiar Junior Samu |
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The Correlation of
Open access Macedonian journal of medical sciences 2019 Jun 7 (12): 1940-1945. Rachmawati Meike, Yulianti Herry, Hernowo Bethy S, Suryanti Sri, Wijaya Indra, Rahadiani Nur, Heriyanto Didik S, Irianiwati Irianiwa |
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Relapsed and De Novo Metastatic HER2-positive Breast Cancer Treated With Trastuzumab: Tumor Genotypes and Clinical Measures Associated With Patient Outcome.
Clinical breast cancer 2019 Apr 19 (2): 113-125.e4. Kotoula Vassiliki, Tsakiri Kalliopi, Koliou Georgia-Angeliki, Lazaridis Georgios, Papadopoulou Kyriaki, Giannoulatou Eleni, Tikas Ioannis, Christodoulou Christos, Chatzopoulos Kyriakos, Bobos Mattheos, Pentheroudakis George, Tsolaki Eleftheria, Batistatou Anna, Kotsakis Athanassios, Koutras Angelos, Linardou Helena, Razis Evangelia, Res Eleni, Pectasides Dimitrios, Fountzilas Geor |
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Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosa.
International ophthalmology 2019 Apr . Roshandel Danial, Rafati Maryam, Khorami Sara, Novin Baheran Nima, Jalali Setareh, Tabatabaie Razieh, Rezai Safura, Ahmadieh Hamid, Ghaffari Saeed Re |
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Rare, low-frequency and common coding variants of ARHGEF28 gene and their association with sporadic amyotrophic lateral sclerosis.
Neurobiology of aging 2019 Mar . Song Yang, Lin Feng, Ye Cheng-Hui, Huang Huaping, Li Xuying, Yao Xiaoli, Xu Yanming, Wang Chaodo |
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Relationships Between Adipose Mitochondrial Function, Serum Adiponectin, and Insulin Resistance in Persons With HIV After 96 Weeks of Antiretroviral Therapy.
Journal of acquired immune deficiency syndromes (1999) 2019 Mar 80 (3): 358-366. Hulgan Todd, Ramsey Benjamin S, Koethe John R, Samuels David C, Gerschenson Mariana, Libutti Daniel E, Sax Paul E, Daar Eric S, McComsey Grace A, Brown Todd |
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Evaluation of bone disease in patients with cystic fibrosis and end-stage lung disease.
Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia 2019 Feb 45 (1): e20170280. Robinson Cécile A, Hofer Markus, Benden Christian, Schmid Christo |
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Association of HLA Class II alleles and Haplotypes with Type 1 Diabetes in Tunisian Arabs.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2018 Nov . Hajjej Abdelhafidh, Almawi Wassim Y, Stayoussef Mouna, Hattab Lasmar, Hmida Sla |
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Cardiovascular risk and mannose binding lectin in patients with rheumatoid arthritis from southern Brazil.
International journal of cardiology. Heart & vasculature 2018 Sep 20 27-31. Kahlow Barbara S, Nisihara Renato, Petisco Roberta, Utiyama Shirley R R, Messias-Reason Iara J, Goeldner Isabela, Skare Thelma |
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Effect of rs3910105 in the Synuclein Gene on Dopamine Transporter Availability in Healthy Subjects.
Yonsei medical journal 2018 Aug 59 (6): 787-792. Seo Youngduk, Pak Kyoungjune, Nam Hyun Yeol, Seok Ju Won, Lee Myung Jun, Kim Eun Joo, Lee Jae Meen, Kim Seong Jang, Kim In J |
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Rho Guanine Nucleotide Exchange Factor ARHGEF17 Is a Risk Gene for Intracranial Aneurysms.
Circulation. Genomic and precision medicine 2018 Jul 11 (7): e002099. Yang Xinyu, Li Jiani, Fang Yabo, Zhang Zhen, Jin Daqing, Chen Xingdong, Zhao Yan, Li Mengqi, Huan Linchun, Kent Thomas A, Dong Jing-Fei, Jiang Rongcai, Yang Shuyuan, Jin Li, Zhang Jianning, Zhong Tao P, Yu Fu |
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The Updated AJCC/TNM Staging System for Papillary Thyroid Cancer (8th Edition): From the Perspective of Genomic Analysis.
World journal of surgery 2018 May . Kim Kyubo, Kim Jin Hwan, Park Il Seok, Rho Young Soo, Kwon Gee Hwan, Lee Dong J |
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Novel HLA class I associations with HIV-1 control in a unique genetically admixed population.
Scientific reports 2018 Apr 8 (1): 6111. Valenzuela-Ponce Humberto, Alva-Hernández Selma, Garrido-Rodríguez Daniela, Soto-Nava Maribel, García-Téllez Thalía, Escamilla-Gómez Tania, García-Morales Claudia, Quiroz-Morales Verónica Sonia, Tapia-Trejo Daniela, Del Arenal-Sánchez Silvia, Prado-Galbarro Francisco-Javier, Hernández-Juan Ramón, Rodríguez-Aguirre Edna, Murakami-Ogasawara Akio, Mejía-Villatoro Carlos, Escobar-Urias Ingrid Y, Pinzón-Meza Rodolfo, Pascale Juan Miguel, Zaldivar Yamitzel, Porras-Cortés Guillermo, Quant-Durán Carlos, Lorenzana Ivette, Meza Rita I, Palou Elsa Y, Manzanero Marvin, Cedillos Rolando A, Aláez Carmen, Brockman Mark A, Harrigan P Richard, Brumme Chanson J, Brumme Zabrina L, Ávila-Ríos Santiago, Reyes-Terán Gustavo, |
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Common variants of ROCKs and the risk of hypertension, and stroke: Two case-control studies and a follow-up study in Chinese Han population.
Biochimica et biophysica acta. Molecular basis of disease 2018 Mar 1864 (3): 778-783. Yang Song, Zhao Yanping, Tian Yuanrui, Chen Yanchun, Zhao Xianghai, Li Ying, Zhao Hailong, Chen Xiaotian, Zhu Lijun, Fang Zhengmei, Yao YingShui, Hu Zhibing, Shen Cho |
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Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8.
Translational psychiatry 2018 Feb 8 (1): 40. McElroy Susan L, Winham Stacey J, Cuellar-Barboza Alfredo B, Colby Colin L, Ho Ada Man-Choi, Sicotte Hugues, Larrabee Beth R, Crow Scott, Frye Mark A, Biernacka Joanna |
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C3-epimerization of 25-hydroxyvitamin D increases with increasing serum 25-hydroxyvitamin D levels and shows a high degree of tracking over time.
Clinical biochemistry 2018 Feb . Kubiak Julia M, Grimnes Guri, Cashman Kevin D, Kamycheva Elena, Dowling Kirsten, Skrabáková Zuzana, Jorde Ro |
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Feasibility of monitoring advanced melanoma patients using cell-free DNA from plasma.
Pigment cell & melanoma research 2018 01 31 (1): 73-81. Gangadhar Tara C, Savitch Samantha L, Yee Stephanie S, Xu Wei, Huang Alexander C, Harmon Shannon, Lieberman David B, Soucier Devon, Fan Ryan, Black Taylor A, Morrissette Jennifer J D, Salathia Neeraj, Waters Jill, Zhang Shile, Toung Jonathan, van Hummelen Paul, Fan Jian-Bing, Xu Xiaowei, Amaravadi Ravi K, Schuchter Lynn M, Karakousis Giorgos C, Hwang Wei-Ting, Carpenter Erica |
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T cell activation Rho GTPase activating protein (TAGAP) is upregulated in clinical and experimental arthritis.
Cytokine 2018 04 104 130-135. Arshad Maria, Bhatti Attya, John Peter, Jalil Fazal, Borghese Federica, Kawalkowska Joanna Z, Williams Richard O, Clanchy Felix I |
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Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility.
PloS one 2018 13 (7): e0197561. Earp Madalene, Tyrer Jonathan P, Winham Stacey J, Lin Hui-Yi, Chornokur Ganna, Dennis Joe, Aben Katja K H, Anton-Culver Hoda, Antonenkova Natalia, Bandera Elisa V, Bean Yukie T, Beckmann Matthias W, Bjorge Line, Bogdanova Natalia, Brinton Louise A, Brooks-Wilson Angela, Bruinsma Fiona, Bunker Clareann H, Butzow Ralf, Campbell Ian G, Carty Karen, Chang-Claude Jenny, Cook Linda S, Cramer Daniel W, Cunningham Julie M, Cybulski Cezary, Dansonka-Mieszkowska Agnieszka, Despierre Evelyn, Doherty Jennifer A, Dörk Thilo, du Bois Andreas, Dürst Matthias, Easton Douglas F, Eccles Diana M, Edwards Robert P, Ekici Arif B, Fasching Peter A, Fridley Brooke L, Gentry-Maharaj Aleksandra, Giles Graham G, Glasspool Rosalind, Goodman Marc T, Gronwald Jacek, Harter Philipp, Hein Alexander, Heitz Florian, Hildebrandt Michelle A T, Hillemanns Peter, Hogdall Claus K, Høgdall Estrid, Hosono Satoyo, Iversen Edwin S, Jakubowska Anna, Jensen Allan, Ji Bu-Tian, Jung Audrey Y, Karlan Beth Y, Kellar Melissa, Kiemeney Lambertus A, Kiong Lim Boon, Kjaer Susanne K, Krakstad Camilla, Kupryjanczyk Jolanta, Lambrechts Diether, Lambrechts Sandrina, Le Nhu D, Lele Shashi, Lester Jenny, Levine Douglas A, Li Zheng, Liang Dong, Lissowska Jolanta, Lu Karen, Lubinski Jan, Lundvall Lene, Massuger Leon F A G, Matsuo Keitaro, McGuire Valerie, McLaughlin John R, McNeish Iain, Menon Usha, Milne Roger L, Modugno Francesmary, Moysich Kirsten B, Ness Roberta B, Nevanlinna Heli, Odunsi Kunle, Olson Sara H, Orlow Irene, Orsulic Sandra, Paul James, Pejovic Tanja, Pelttari Liisa M, Permuth Jenny B, Pike Malcolm C, Poole Elizabeth M, Rosen Barry, Rossing Mary Anne, Rothstein Joseph H, Runnebaum Ingo B, Rzepecka Iwona K, Schernhammer Eva, Schwaab Ira, Shu Xiao-Ou, Shvetsov Yurii B, Siddiqui Nadeem, Sieh Weiva, Song Honglin, Southey Melissa C, Spiewankiewicz Beata, Sucheston-Campbell Lara, Tangen Ingvild L, Teo Soo-Hwang, Terry Kathryn L, Thompson Pamela J, Thomsen Lotte, Tworoger Shelley S, van Altena Anne M, Vergote Ignace, Vestrheim Thomsen Liv Cecilie, Vierkant Robert A, Walsh Christine S, Wang-Gohrke Shan, Wentzensen Nicolas, Whittemore Alice S, Wicklund Kristine G, Wilkens Lynne R, Woo Yin-Ling, Wu Anna H, Wu Xifeng, Xiang Yong-Bing, Yang Hannah, Zheng Wei, Ziogas Argyrios, Lee Alice W, Pearce Celeste L, Berchuck Andrew, Schildkraut Joellen M, Ramus Susan J, Monteiro Alvaro N A, Narod Steven A, Sellers Thomas A, Gayther Simon A, Kelemen Linda E, Chenevix-Trench Georgia, Risch Harvey A, Pharoah Paul D P, Goode Ellen L, Phelan Catherine |
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
The Lancet. Respiratory medicine 2017 Nov 5 (11): 869-880. Allen Richard J, Porte Joanne, Braybrooke Rebecca, Flores Carlos, Fingerlin Tasha E, Oldham Justin M, Guillen-Guio Beatriz, Ma Shwu-Fan, Okamoto Tsukasa, John Alison E, Obeidat Ma'en, Yang Ivana V, Henry Amanda, Hubbard Richard B, Navaratnam Vidya, Saini Gauri, Thompson Norma, Booth Helen L, Hart Simon P, Hill Mike R, Hirani Nik, Maher Toby M, McAnulty Robin J, Millar Ann B, Molyneaux Philip L, Parfrey Helen, Rassl Doris M, Whyte Moira K B, Fahy William A, Marshall Richard P, Oballa Eunice, Bossé Yohan, Nickle David C, Sin Don D, Timens Wim, Shrine Nick, Sayers Ian, Hall Ian P, Noth Imre, Schwartz David A, Tobin Martin D, Wain Louise V, Jenkins R Gis |
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KRAS Mutation in Gastric Cancer and Prognostication Associated with Microsatellite Instability Status.
Pathology oncology research : POR 2017 Nov . Polom Karol, Das Kakoli, Marrelli Daniele, Roviello Giandomenico, Pascale Valeria, Voglino Costantino, Rho Henry, Tan Patrick, Roviello Fran |
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The SRGAP2 SNPs, their haplotypes and G?×?E interactions on serum lipid traits.
Scientific reports 2017 Sep 7 (1): 11626. Miao Liu, Yin Rui-Xing, Wu Jin-Zhen, Yang Shuo, Lin Wei-Xiong, Pan Shang-Li |
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Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.
Headache 2017 Jul 57 (7): 1118-1135. García-Martín Elena, Martínez Carmen, Serrador Mercedes, Alonso-Navarro Hortensia, Navacerrada Francisco, Esguevillas Gara, García-Albea Esteban, Agúndez José A G, Jiménez-Jiménez Félix Javi |
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Relationship between soluble CD25 and gene expression in healthy individuals and patients with multiple sclerosis.
Cytokine 2017 May . Buhelt Sophie, Ratzer Rikke Lenhard, Christensen Jeppe Romme, Börnsen Lars, Sellebjerg Finn, Søndergaard Helle Ba |
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Relationship Between C-Reactive Protein Serum Concentration and the 1846 C>T (rs1205) Polymorphism in Patients with Acute Coronary Syndrome from Western Mexico.
Genetic testing and molecular biomarkers 2017 Mar . Reynoso-Villalpando Gabriela Lizet, Padilla-Gutiérrez Jorge Ramón, Valdez-Haro Angélica, Casillas-Muñoz Fidel, Muñoz-Valle José Francisco, Castellanos-Nuñez Edgar, Chávez-Herrera Juan Carlos, Valle Yemin |
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Association of LPP and TAGAP Polymorphisms with Celiac Disease Risk: A Meta-Analysis.
International journal of environmental research and public health 2017 Feb 14 (2): . Huang Shi-Qi, Zhang Na, Zhou Zi-Xing, Huang Chui-Can, Zeng Cheng-Li, Xiao Di, Guo Cong-Cong, Han Ya-Jing, Ye Xiao-Hong, Ye Xing-Guang, Ou Mei-Ling, Zhang Bao-Huan, Liu Yang, Zeng Eddy Y, Yang Guang, Jing Chun-X |
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Association of VAV2 and VAV3 polymorphisms with cardiovascular risk factors.
Scientific reports 2017 Feb 7 41875. Perretta-Tejedor Nuria, Fernández-Mateos Javier, García-Ortiz Luis, Gómez-Marcos Manuel A, Recio-Rodríguez José I, Agudo-Conde Cristina, Rodriguez-Sánchez Emiliano, Morales Ana I, López-Hernández Francisco J, López-Novoa José M, González-Sarmiento Rogelio, Martínez-Salgado Carl |
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High prevalence of mutations affecting the splicing process in a Spanish cohort with autosomal dominant retinitis pigmentosa.
Scientific reports 2017 Jan 7 39652. Ezquerra-Inchausti Maitane, Barandika Olatz, Anasagasti Ander, Irigoyen Cristina, López de Munain Adolfo, Ruiz-Ederra Javi |
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Effect of PICALM rs3851179 polymorphism on the default mode network function in mild cognitive impairment.
Behavioural brain research 2017 07 331 225-232. Sun Ding-Ming, Chen Hai-Feng, Zuo Qi-Long, Su Fan, Bai Feng, Liu Chun-Fe |
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Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
Nature communications 2017 06 8 15789. Sigurdsson Snaevar, Alexandersson Kristjan F, Sulem Patrick, Feenstra Bjarke, Gudmundsdottir Steinunn, Halldorsson Gisli H, Olafsson Sigurgeir, Sigurdsson Asgeir, Rafnar Thorunn, Thorgeirsson Thorgeir, Sørensen Erik, Nordholm-Carstensen Andreas, Burcharth Jakob, Andersen Jens, Jørgensen Henrik Stig, Possfelt-Møller Emma, Ullum Henrik, Thorleifsson Gudmar, Masson Gisli, Thorsteinsdottir Unnur, Melbye Mads, Gudbjartsson Daniel F, Stefansson Tryggvi, Jonsdottir Ingileif, Stefansson Ka |
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ARHGEF10 gene polymorphism is closely associated with the risk of ischemic stroke in Northern Han Chinese population.
Neurological research 2016 Dec 1-7. Li Hong, Yu Shasha, Wang Rui, Sun Zhaoqing, Zhou Xinghu, Zheng Liqiang, Yin Zhihua, Zhang Xingang, Sun Yingxi |
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Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing.
Investigative ophthalmology & visual science 2016 Nov 57 (14): 6374-6381. Roberts Lisa, Ratnapriya Rinki, du Plessis Morné, Chaitankar Vijender, Ramesar Raj S, Swaroop Ana |
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Low Gene Dosage of Cdc42 Is Not Associated with Protein Dysfunction in Patients with Colorectal Cancer.
DNA and cell biology 2016 Aug . González-Quiroz Matías, Calderón Ximena, Oyarzún Ingrid, Hoepfner Claudia, Azócar Andrés, Aguirre Adam, Álvarez Karin, Quera Rodrigo, López-Köstner Francisco, Meléndez Jai |
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Rho GTPases: RAC1 polymorphisms affected platinum-based chemotherapy toxicity in lung cancer patients.
Cancer chemotherapy and pharmacology 2016 Aug 78 (2): 249-58. Zou Ting, Yin Jiye, Zheng Wei, Xiao Ling, Tan Liming, Chen Juan, Wang Ying, Li Xiangping, Qian Chenyue, Cui Jiajia, Zhang Wei, Zhou Honghao, Liu Zhaoqi |
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SERUM LEVELS OF CARCINOEMBRYONIC ANTIGEN (CEA) IN PATIENTS WITH TYPE 2 DIABETES.
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2016 Aug . Zayed Ayman A, Beano Abdallah M, Amer Farah N, Maslamani Jumana M, Zmaili Mohammad A, Al-Khudary Talha H, Yousef Al-Motassem |
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HMSH2 and HMSH6 gene expression profiles in colorectal adenocarcinoma in patients up to 50 years of age.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2016 Jul 83 602-606. Germini Demétrius, Gehrke Flávia, Lira Daniel, Alves Beatriz, Azzalis Lígia, Perez Matheus, Fonseca Fernando, Waisberg Jaqu |
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The importance of sustained attention in early Alzheimer's disease.
International journal of geriatric psychiatry 2016 Jul . Huntley Jonathan D, Hampshire Adam, Bor Daniel, Owen Adrian M, Howard Robert |
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VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone.
Genetic testing and molecular biomarkers 2016 Jun 20 (6): 335-7. Usategui-Martín Ricardo, Calero-Paniagua Ismael, García-Aparicio Judith, Corral-Gudino Luis, Del Pino Montes Javier, González Sarmiento Rogel |
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Association of Rho-kinase Gene Polymorphisms with Respiratory Distress Syndrome in Preterm Neonates.
Pediatrics and neonatology 2016 May . Kaya Gül, Sivasli Ercan, Oztuzcu Serdar, Melekoglu Nuriye A, Ozkara Esma, Sarikabadayi Unal, Demiryürek Abdullah |
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High-risk and low-risk gastric cancer areas in Italy and its association with microsatellite instability.
Journal of cancer research and clinical oncology 2016 May . Polom Karol, Marrelli Daniele, Pascale Valeria, Roviello Giandomenico, Voglino Costantino, Rho Henry, Vindigni Carla, Marini Mario, Macchiarelli Raffaele, Roviello Fran |
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Toward Novel Diagnostics for Primary Open-Angle Glaucoma? An Association Study of Polymorphic Variation in Ras Homolog Family Member (A, B, C, D) Genes RHOA, RHOB, RHOC, and RHOD.
Omics : a journal of integrative biology 2016 May 20 (5): 290-5. Saracaloglu Ahmet, Demiryürek Seniz, Okumus Seydi, Oztuzcu Serdar, Bozgeyik Ibrahim, Coskun Erol, Aksoy Umit, Kaydu Erdal, Erbagci Ibrahim, Gürler Bulent, Alasehirli Belgin, Demiryürek Abdullah |
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GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.
BMC genomics 2016 Apr 17 276. Chittoor Geetha, Kent Jack W, Almeida Marcio, Puppala Sobha, Farook Vidya S, Cole Shelley A, Haack Karin, Göring Harald H H, MacCluer Jean W, Curran Joanne E, Carless Melanie A, Johnson Matthew P, Moses Eric K, Almasy Laura, Mahaney Michael C, Lehman Donna M, Duggirala Ravindranath, Comuzzie Anthony G, Blangero John, Voruganti Venkata Saro |
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Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual.
Investigative ophthalmology & visual science 2016 Mar 57 (3): 940-7. Beryozkin Avigail, Levy Gal, Blumenfeld Anat, Meyer Segev, Namburi Prasanthi, Morad Yair, Gradstein Libe, Swaroop Anand, Banin Eyal, Sharon Dr |
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CT Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism.
Chest 2016 Jan . Chung Jonathan H, Peljto Anna L, Chawla Ashish, Talbert Janet L, McKean David F, Rho Byung-Hak, Fingerlin Tasha E, Schwarz Marvin I, Schwartz David A, Lynch David |
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Genetic alterations and their clinical implications in gastric cancer peritoneal carcinomatosis revealed by whole-exome sequencing of malignant ascites.
Oncotarget 2016 Jan . Lim Byungho, Kim Chan, Kim Jeong-Hwan, Kwon Woo Sun, Lee Won Seok, Kim Jeong Min, Park Jun Yong, Kim Hyo Song, Park Kyu Hyun, Kim Tae Soo, Park Jong-Lyul, Chung Hyun Cheol, Rha Sun Young, Kim Seon-You |
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Whole-exome Sequencing analyses of Inflammatory Bowel Disease-associated Colorectal Cancers.
Gastroenterology 2016 Jan . Robles Ana I, Traverso Giovanni, Zhang Ming, Roberts Nicholas J, Khan Mohammed A, Joseph Christine, Lauwers Gregory Y, Selaru Florin M, Popoli Maria, Pittman Meredith E, Ke Xiquan, Hruban Ralph H, Meltzer Stephen J, Kinzler Kenneth W, Vogelstein Bert, Harris Curtis C, Papadopoulos Nickol |
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An Alzheimer's Disease-Derived Biomarker Signature Identifies Parkinson's Disease Patients with Dementia.
PloS one 2016 11 (1): e0147319. Berlyand Yosef, Weintraub Daniel, Xie Sharon X, Mellis Ian A, Doshi Jimit, Rick Jacqueline, McBride Jennifer, Davatzikos Christos, Shaw Leslie M, Hurtig Howard, Trojanowski John Q, Chen-Plotkin Alice |
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Association of RAC1 Gene Polymorphisms with Primary End-Stage Renal Disease in Chinese Renal Recipients.
PloS one 2016 11 (2): e0148270. Liu Yani, Zhou Jiali, Luo Xiaomei, Yang Chunxiao, Zhang Yu, Shi Shaoj |
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Genome-Wide Association of Heroin Dependence in Han Chinese.
PloS one 2016 11 (12): e0167388. Kalsi Gursharan, Euesden Jack, Coleman Jonathan R I, Ducci Francesca, Aliev Fazil, Newhouse Stephen J, Liu Xiehe, Ma Xiaohong, Wang Yingcheng, Collier David A, Asherson Philip, Li Tao, Breen Gero |
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Polymorphisms and haplotype of ROCK2 associate with high altitude essential hypertension in native high altitude Ladakhi Indian population: a preliminary study.
Clinical and experimental hypertension (New York, N.Y. : 1993) 2016 38 (2): 238-44. Pandey Priyanka, Mohammad Ghulam, Singh Yogendra, Pasha M A Qad |
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Predictive factors for a long-term response duration in non-squamous cell lung cancer patients treated with pemetrexed.
BMC cancer 2016 16 417. Park Sojung, Kim Hyun Jung, Choi Chang-Min, Lee Dae Ho, Kim Sang-We, Lee Jung-Shin, Kim Woo Sung, Choi Se Hoon, Rho Jin Kyung, Lee Jae Che |
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Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population.
Investigative ophthalmology & visual science 2015 Dec 56 (13): 8297-305. Coussa Razek Georges, Chakarova Christina, Ajlan Radwan, Taha Mohammed, Kavalec Conrad, Gomolin Julius, Khan Ayesha, Lopez Irma, Ren Huanan, Waseem Naushin, Kamenarova Kunka, Bhattacharya Shomi S, Koenekoop Robert |
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Whole exome sequencing identifies rare protein-coding variants in Behçet's disease.
Arthritis & rheumatology (Hoboken, N.J.) 2015 Dec . Ognenovski Mikhail, Renauer Paul, Gensterblum Elizabeth, Kötter Ina, Xenitidis Theodoros, Henes Jörg C, Casali Bruno, Salvarani Carlo, Direskeneli Haner, Kaufman Kenneth M, Sawalha Amr |
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The association between olfactory bulb volume, cognitive dysfunction, physical disability and depression in multiple sclerosis.
European journal of neurology 2015 Nov . Yaldizli Ö, Penner I-K, Yonekawa T, Naegelin Y, Kuhle J, Pardini M, Chard D T, Stippich C, Kira J-I, Bendfeldt K, Amann M, Radue E-W, Kappos L, Sprenger |
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Analysis of Mutations in Epidermal Growth Factor Receptor Gene in Korean Patients with Non-small Cell Lung Cancer: Summary of a Nationwide Survey.
Journal of pathology and translational medicine 2015 Oct . Lee Sang Hwa, Kim Wan Seop, Choi Yoo Duk, Seo Jeong Wook, Han Joung Ho, Kim Mi Jin, Kim Lucia, Lee Geon Kook, Lee Chang Hun, Oh Mee Hye, Kim Gou Young, Sung Sun Hee, Lee Kyo Young, Chang Sun Hee, Rho Mee Sook, Kim Han Kyeom, Jung Soon Hee, Jang Se Jin, |
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Association of the EGF-TM7 receptor CD97 expression with FLT3-ITD in acute myeloid leukemia.
Oncotarget 2015 Oct . Wobus Manja, Bornhäuser Martin, Jacobi Angela, Kräter Martin, Otto Oliver, Ortlepp Claudia, Guck Jochen, Ehninger Gerhard, Thiede Christian, Oelschlägel U |
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Osteoprotegerin (OPG), The Endogenous Inhibitor of Receptor Activator of NF-?B Ligand (RANKL), is Dysregulated in BRCA Mutation Carriers.
EBioMedicine 2015 Oct 2 (10): 1331-9. Widschwendter Martin, Burnell Matthew, Fraser Lindsay, Rosenthal Adam N, Philpott Sue, Reisel Daniel, Dubeau Louis, Cline Mark, Pan Yang, Yi Ping-Cheng, Gareth Evans D, Jacobs Ian J, Menon Usha, Wood Charles E, Dougall William |
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Computing a Synthetic Chronic Psychosocial Stress Measurement in Multiple Datasets and its Application in the Replication of G × E Interactions of the EBF1 Gene.
Genetic epidemiology 2015 Sep 39 (6): 489-97. Singh Abanish, Babyak Michael A, Brummett Beverly H, Jiang Rong, Watkins Lana L, Barefoot John C, Kraus William E, Shah Svati H, Siegler Ilene C, Hauser Elizabeth R, Williams Redford |
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Analyzing large-scale samples highlights significant association between rs10411210 polymorphism and colorectal cancer.
Biomedicine & pharmacotherapy = Biome?decine & pharmacothe?rapie 2015 Aug 74 164-8. He Dongfeng, Ma Lihong, Feng Rennan, Zhang Liangcai, Jiang Yongshuai, Zhang Yanqiao, Liu Guiy |
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Genetics of serum concentration of IL-6 and TNF? in systemic lupus erythematosus and rheumatoid arthritis: a candidate gene analysis.
Clinical rheumatology 2015 Aug 34 (8): 1375-82. Solus Joseph F, Chung Cecilia P, Oeser Annette, Li Chun, Rho Young Hee, Bradley Kevin M, Kawai Vivian K, Smith Jeffrey R, Stein C Micha |
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Investigation Of Rho-Kinase Expressions And Polymorphisms In Mantle Cell Lymphoma Patients.
Turkish journal of haematology : official journal of Turkish Society of Haematology 2015 Aug . Yanarda? Aç?k Didar, Y?lmaz Mehmet, Sar? ?brahim, Öztuzcu Serdar, Say?ner Zeynel A, Subari Salih, Demiryürek Abdullah |
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Investigation of the Rho-kinase Gene Polymorphism in Primary Open-angle Glaucoma.
Ophthalmic genetics 2015 Aug 1-4. Demiryürek Seniz, Okumus Seydi, Bozgeyik ?brahim, Oztuzcu Serdar, Coskun Erol, Mat Emrah, Durucu Ela, Tatar Mehmet G, Erbagci ?brahim, Gürler Bülent, Demiryürek Abdullah |
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Association of Rho/Rho-kinase gene polymorphisms and expressions with obesity-related metabolic syndrome.
European review for medical and pharmacological sciences 2015 May 19 (9): 1680-8. Tabur S, Oztuzcu S, Oguz E, Korkmaz H, Eroglu S, Ozkaya M, Demiryürek A |
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Association of substance dependence phenotypes in the COGA sample.
Addiction biology 2015 May 20 (3): 617-27. Wetherill Leah, Agrawal Arpana, Kapoor Manav, Bertelsen Sarah, Bierut Laura J, Brooks Andrew, Dick Danielle, Hesselbrock Michie, Hesselbrock Victor, Koller Daniel L, Le Nhung, Nurnberger John I, Salvatore Jessica E, Schuckit Marc, Tischfield Jay A, Wang Jen-Chyong, Xuei Xiaoling, Edenberg Howard J, Porjesz Bernice, Bucholz Kathleen, Goate Alison M, Foroud Tatia |
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Low protective PON1 lactonase activity in an Arab population with high rates of coronary heart disease and diabetes.
Clinica chimica acta; international journal of clinical chemistry 2015 May 445 41-7. Gugliucci A, Caccavello R, Nassar H, Abu Ahmad W, Sinnreich R, Kark J |
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Common genetic variants in epigenetic machinery genes and risk of upper gastrointestinal cancers.
International journal of epidemiology 2015 Apr . Sung Hyuna, Yang Howard H, Zhang Han, Yang Qi, Hu Nan, Tang Ze-Zhong, Su Hua, Wang Lemin, Wang Chaoyu, Ding Ti, Fan Jin-Hu, Qiao You-Lin, Wheeler William, Giffen Carol, Burdett Laurie, Wang Zhaoming, Lee Maxwell P, Chanock Stephen J, Dawsey Sanford M, Freedman Neal D, Abnet Christian C, Goldstein Alisa M, Yu Kai, Taylor Philip R, Hyland Paula |
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ERAP1 gene expression is influenced by non-synonymous polymorphisms associated with predisposition to spondyloarthritis.
Arthritis & rheumatology (Hoboken, N.J.) 2015 Mar . Costantino Félicie, Talpin Alice, Evnouchidou Irini, Kadi Amir, Leboime Ariane, Said-Nahal Roula, Bonilla Nelly, Letourneur Franck, Leturcq Tifenn, Ka Zeyna, van Endert Peter, Garchon Henri-Jean, Chiocchia Gilles, Breban Maxi |
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Follow-up to genome-wide linkage and admixture mapping studies implicates components of the extracellular matrix in susceptibility to and size of uterine fibroids.
Fertility and sterility 2015 Feb 103 (2): 528-34.e13. Aissani Brahim, Zhang Kui, Wiener Howa |
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Prevalence of Rhodopsin mutations in autosomal dominant Retinitis Pigmentosa in Spain: clinical and analytical review in 200 families.
Acta ophthalmologica 2015 Feb 93 (1): e38-44. Fernandez-San Jose Patricia, Blanco-Kelly Fiona, Corton Marta, Trujillo-Tiebas Maria-Jose, Gimenez Ascension, Avila-Fernandez Almudena, Garcia-Sandoval Blanca, Lopez-Molina Maria-Isabel, Hernan Inma, Carballo Miguel, Riveiro-Alvarez Rosa, Ayuso Carm |
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Two functional polymorphisms of ROCK2 enhance arterial stiffening through inhibiting its activity and expression.
Journal of molecular and cellular cardiology 2015 Feb 79 180-6. Liao Yi-Chu, Liu Ping-Yen, Lin Hsiu-Fen, Lin Wen-Yi, Liao James K, Juo Suh-Hang |
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Haplotypes of RHO polymorphisms and susceptibility to age-related macular degeneration.
International journal of clinical and experimental pathology 2015 8 (3): 3174-9. Tang Kun, Wang Wei, Wang Qun, Wang Liqiang, Bai Hua, Jiang Yanming, Huang Yif |
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Possible Gender-Related Modulation by the ROCK1 Gene in Colorectal Cancer Susceptibility.
Pathobiology : journal of immunopathology, molecular and cellular biology 2015 82 (6): 252-8. Zucchini Cinzia, Martinelli Marcella, De Sanctis Paola, Rodia Maria Teresa, Mattei Gabriella, Ugolini Giampaolo, Montroni Isacco, Ghignone Federico, Solmi Rossel |
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Severity of Mitral Valve Degeneration Is Associated with Chromosome 15 Loci in Whippet Dogs.
PloS one 2015 10 (10): e0141234. Stern Joshua A, Hsue Weihow, Song Kun-Ho, Ontiveros Eric S, Luis Fuentes Virginia, Stepien Rebecca |
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Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) 2014 Dec . Sorosina Melissa, Esposito Federica, Guaschino Clara, Clarelli Ferdinando, Barizzone Nadia, Osiceanu Ana Maria, Brambilla Paola, Mascia Elisabetta, Cavalla Paola, Gallo Paolo, , , Martinelli Vittorio, Leone Maurizio, Comi Giancarlo, D'Alfonso Sandra, Martinelli Boneschi Filip |
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Significance of allelic percentage of BRAF c.1799T > A (V600E) mutation in papillary thyroid carcinoma.
Annals of surgical oncology 2014 Dec 21 Suppl 4 S619-26. Cheng Shih-Ping, Hsu Yi-Chiung, Liu Chien-Liang, Liu Tsang-Pai, Chien Ming-Nan, Wang Tao-Yeuan, Lee Jie-J |
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Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing.
Investigative ophthalmology & visual science 2014 Nov 55 (11): 7369-75. Oishi Maho, Oishi Akio, Gotoh Norimoto, Ogino Ken, Higasa Koichiro, Iida Kei, Makiyama Yukiko, Morooka Satoshi, Matsuda Fumihiko, Yoshimura Nagahi |
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FGFR1 amplification is associated with poor prognosis and smoking in non-small-cell lung cancer.
Virchows Archiv : an international journal of pathology 2014 Nov 465 (5): 547-58. Seo An Na, Jin Yan, Lee Hee Jin, Sun Ping-Li, Kim Hyojin, Jheon Sanghoon, Kim Kwhanmien, Lee Choon-Taek, Chung Jin-Hae |
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Human Rho guanine nucleotide exchange factor 11 gene is associated with schizophrenia in a Japanese population.
Human psychopharmacology 2014 Nov 29 (6): 552-8. Mizuki Yutaka, Takaki Manabu, Okahisa Yuko, Sakamoto Shinji, Kodama Masafumi, Ujike Hiroshi, Uchitomi Yosu |
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Association of Rho-kinase 1 (ROCK1) gene polymorphisms with Behçet's disease.
Molecular diagnosis & therapy 2014 Aug 18 (4): 419-26. Oguz Elif, Demiryürek Abdullah Tuncay, Pehlivan Yavuz, Kisacik Bünyamin, Ozkara Esma, Oztuzcu Serdar, Alasehirli Belgin, Onat Ahmet Mes |
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Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample.
Neurobiology of aging 2014 Jun 35 (6): 1510.e1-5. Fahey Ciara, Byrne Susan, McLaughlin Russell, Kenna Kevin, Shatunov Aleksey, Donohoe Gary, Gill Michael, Al-Chalabi Ammar, Bradley Daniel G, Hardiman Orla, Corvin Aiden P, Morris Derek |
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Expression of selected genes in liver biopsy specimens in relation to early virological response in patients with chronic hepatitis C with HCV mono- and HIV/HCV co-infection.
Archives of virology 2014 Jun 159 (6): 1365-71. Jab?onowska El?bieta, Wójcik Kamila, Ko?li?ska-Berkan Ewa, Szyma?ska Bo?ena, Omulecka Aleksandra, Piekarska An |
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Gene variations of ROCKs and risk of ischaemic stroke: the Women's Genome Health Study.
Clinical science (London, England : 1979) 2014 Jun 126 (12): 829-35. Zee Robert Y L, Wang Qing-Mei, Chasman Daniel I, Ridker Paul M, Liao James |
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Counterphase modulation flicker photometry: phenotypic and genotypic associations.
Journal of the Optical Society of America. A, Optics, image science, and vision 2014 Apr 31 (4): A226-31. Lawrance-Owen A J, Bosten J M, Hogg R E, Bargary G, Goodbourn P T, Mollon J |
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The clinical application of ABCB1 genotyping in antidepressant treatment: a pilot study.
CNS spectrums 2014 Apr 19 (2): 165-75. Breitenstein Barbara, Scheuer Sandra, Pfister Hildegard, Uhr Manfred, Lucae Susanne, Holsboer Florian, Ising Marcus, Brückl Tanja |
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Loss of fat-free mass over four years in adult cystic fibrosis is associated with high serum interleukin-6 levels but not tumour necrosis factor-alpha.
Clinical nutrition (Edinburgh, Scotland) 2014 Feb 33 (1): 150-5. King Susannah J, Nyulasi Ibolya B, Bailey Michael, Kotsimbos Tom, Wilson John |
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Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
European journal of human genetics : EJHG 2014 Jan 22 (1): 99-104. Glöckle Nicola, Kohl Susanne, Mohr Julia, Scheurenbrand Tim, Sprecher Andrea, Weisschuh Nicole, Bernd Antje, Rudolph Günther, Schubach Max, Poloschek Charlotte, Zrenner Eberhart, Biskup Saskia, Berger Wolfgang, Wissinger Bernd, Neidhardt Jo |
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TCF4 gene polymorphism and cognitive performance in patients with first episode psychosis.
Schizophrenia research 2014 Jan 152 (1): 124-9. Albanna Ammar, Choudhry Zia, Harvey Philippe-Olivier, Fathalli Ferid, Cassidy Clifford, Sengupta Sarojini M, Iyer Srividya N, Rho Aldanie, Lepage Martin, Malla Ashok, Joober Rid |
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Variants in phospholipid metabolism and upstream regulators and non-small cell lung cancer susceptibility.
Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2014 Jan 16 (1): 107-12. Cebrián A, Taron M, Sala N, Ardanaz E, Chirlaque M-D, Larrañaga N, Redondo M-L, Sánchez M-J, Gómez del Pulgar T, Camps C, Rosell R, González C A, Lacal J |
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Is there any association between childhood cardiac septal defects and ROCK2 gene polymorphism?
Genetics and molecular research : GMR 2014 13 (1): 1949-54. Aksoy M, Uygun H, Baspinar O, Demiryurek S, Oztuzcu S, Cengiz B, Irdem A, Araz N |
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No association between FGD1 gene polymorphisms and intellectual developmental disability in the Qinba mountain area.
Genetics and molecular research : GMR 2014 13 (1): 127-33. Li J L, Li Y J, Zhang K J, Lan L, Shi J G, Yang X, Zhang M J, Zhang F C, Gao X |
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Spectrum of rhodopsin gene mutations in Chinese patients with retinitis pigmentosa.
Molecular vision 2014 20 1132-6. Yang Guoxing, Xie Shipeng, Feng Na, Yuan Zhifeng, Zhang Minglian, Zhao Jialia |
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Syndromic and non-syndromic forms of retinitis pigmentosa: a comprehensive Italian clinical and molecular study reveals new mutations.
Genetics and molecular research : GMR 2014 13 (4): 8815-33. Pierrottet C O, Zuntini M, Digiuni M, Bazzanella I, Ferri P, Paderni R, Rossetti L M, Cecchin S, Orzalesi N, Bertelli |
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Variations in apolipoprotein D and sigma non-opioid intracellular receptor 1 genes with relation to risk, severity and outcome of ischemic stroke.
BMC neurology 2014 14 (1): 191. Lövkvist Håkan, Jönsson Ann-Cathrin, Luthman Holger, Jood Katarina, Jern Christina, Wieloch Tadeusz, Lindgren Ar |
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