Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: DDR1[original query] |
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Linkage and association studies of discoidin domain receptor 1 (DDR1) single nucleotide polymorphisms (SNPs) in juvenile oligoarthritis. Rheumatology (Oxford, England) 2004 Sep 43 (9): 1138-41. Zeggini E, Reginato A M, Prais A, Thomson W, McLean W, Donn R, |
The discoidin domain receptor 1 as a novel susceptibility gene for schizophrenia. Molecular psychiatry 2007 Sep 12 (9): 833-41. Roig B, Virgos C, Franco N, Martorell L, Valero J, Costas J, Carracedo A, Labad A, Vilella |
Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia. Blood 2008 May 111 (9): 4797-808. Tomasson Michael H, Xiang Zhifu, Walgren Richard, Zhao Yu, Kasai Yumi, Miner Tracie, Ries Rhonda E, Lubman Olga, Fremont Daved H, McLellan Michael D, Payton Jacqueline E, Westervelt Peter, DiPersio John F, Link Daniel C, Walter Matthew J, Graubert Timothy A, Watson Mark, Baty Jack, Heath Sharon, Shannon William D, Nagarajan Rakesh, Bloomfield Clara D, Mardis Elaine R, Wilson Richard K, Ley Timothy |
Linkage and association study of discoidin domain receptor 1 as a novel susceptibility gene for childhood IgA nephropathy. International journal of molecular medicine 2010 May 25 (5): 785-91. Hahn Won-Ho, Suh Jin-Soon, Cho Byoung-Soo, Kim Sung- |
Genetic variants of the DDR1 gene are associated with vitiligo in two independent Brazilian population samples. The Journal of investigative dermatology 2010 Jul 130 (7): 1813-8. Silva de Castro Caio Cesar, do Nascimento Liliane Machado, Walker Gaby, Werneck Renata Iani, Nogoceke Everson, Mira Marcelo Távo |
Potential association of DDR1 genetic variant with FEV1 decline by aspirin provocation in asthmatics. The Journal of asthma : official journal of the Association for the Care of Asthma 2012 Apr 49 (3): 237-42. Kim Jason Yongha, Kim Jeong-Hyun, Park Byung-Lae, Pasaje Charisse Flerida A, Bae Joon Seol, Uh Soo-Taek, Kim Yong-Hoon, Kim Mi-Kyeong, Choi Inseon S, Cho Sang Heon, Choi Byoung Whui, Park Jong Sook, Park Choon-Sik, Shin Hyoung D |
Seven new loci associated with age-related macular degeneration.
Nature genetics 2013 Apr 45 (4): 433-9, 439e1-2. Fritsche Lars G, Chen Wei, Schu Matthew, Yaspan Brian L, Yu Yi, Thorleifsson Gudmar, Zack Donald J, Arakawa Satoshi, Cipriani Valentina, Ripke Stephan, Igo Robert P, Buitendijk Gabriëlle H S, Sim Xueling, Weeks Daniel E, Guymer Robyn H, Merriam Joanna E, Francis Peter J, Hannum Gregory, Agarwal Anita, Armbrecht Ana Maria, Audo Isabelle, Aung Tin, Barile Gaetano R, Benchaboune Mustapha, Bird Alan C, Bishop Paul N, Branham Kari E, Brooks Matthew, Brucker Alexander J, Cade William H, Cain Melinda S, Campochiaro Peter A, Chan Chi-Chao, Cheng Ching-Yu, Chew Emily Y, Chin Kimberly A, Chowers Itay, Clayton David G, Cojocaru Radu, Conley Yvette P, Cornes Belinda K, Daly Mark J, Dhillon Baljean, Edwards Albert O, Evangelou Evangelos, Fagerness Jesen, Ferreyra Henry A, Friedman James S, Geirsdottir Asbjorg, George Ronnie J, Gieger Christian, Gupta Neel, Hagstrom Stephanie A, Harding Simon P, Haritoglou Christos, Heckenlively John R, Holz Frank G, Hughes Guy, Ioannidis John P A, Ishibashi Tatsuro, Joseph Peronne, Jun Gyungah, Kamatani Yoichiro, Katsanis Nicholas, N Keilhauer Claudia, Khan Jane C, Kim Ivana K, Kiyohara Yutaka, Klein Barbara E K, Klein Ronald, Kovach Jaclyn L, Kozak Igor, Lee Clara J, Lee Kristine E, Lichtner Peter, Lotery Andrew J, Meitinger Thomas, Mitchell Paul, Mohand-Saïd Saddek, Moore Anthony T, Morgan Denise J, Morrison Margaux A, Myers Chelsea E, Naj Adam C, Nakamura Yusuke, Okada Yukinori, Orlin Anton, Ortube M Carolina, Othman Mohammad I, Pappas Chris, Park Kyu Hyung, Pauer Gayle J T, Peachey Neal S, Poch Olivier, Priya Rinki Ratna, Reynolds Robyn, Richardson Andrea J, Ripp Raymond, Rudolph Guenther, Ryu Euijung, Sahel José-Alain, Schaumberg Debra A, Scholl Hendrik P N, Schwartz Stephen G, Scott William K, Shahid Humma, Sigurdsson Haraldur, Silvestri Giuliana, Sivakumaran Theru A, Smith R Theodore, Sobrin Lucia, Souied Eric H, Stambolian Dwight E, Stefansson Hreinn, Sturgill-Short Gwen M, Takahashi Atsushi, Tosakulwong Nirubol, Truitt Barbara J, Tsironi Evangelia E, Uitterlinden André G, van Duijn Cornelia M, Vijaya Lingam, Vingerling Johannes R, Vithana Eranga N, Webster Andrew R, Wichmann H-Erich, Winkler Thomas W, Wong Tien Y, Wright Alan F, Zelenika Diana, Zhang Ming, Zhao Ling, Zhang Kang, Klein Michael L, Hageman Gregory S, Lathrop G Mark, Stefansson Kari, Allikmets Rando, Baird Paul N, Gorin Michael B, Wang Jie Jin, Klaver Caroline C W, Seddon Johanna M, Pericak-Vance Margaret A, Iyengar Sudha K, Yates John R W, Swaroop Anand, Weber Bernhard H F, Kubo Michiaki, Deangelis Margaret M, Léveillard Thierry, Thorsteinsdottir Unnur, Haines Jonathan L, Farrer Lindsay A, Heid Iris M, Abecasis Gonçalo R, |
Polymorphism of the E-cadherin gene CDH1 is associated with susceptibility to vitiligo. Experimental dermatology 2015 Apr 24 (4): 300-2. Tarlé Roberto Gomes, Silva de Castro Caio Cesar, do Nascimento Liliane Machado, Mira Marcelo Távo |
Identification of miRSNPs associated with the risk of multiple myeloma. International journal of cancer 2016 Oct . Macauda Angelica, Calvetti Diego, Maccari Giuseppe, Hemminki Kari, Försti Asta, Goldschmidt Hartmut, Weinhold Niels, Houlston Richard, Andersen Vibeke, Vogel Ulla, Buda Gabriele, Varkonyi Judit, Sureda Anna, Lopez Joaquin Martinez, Watek Marzena, Butrym Aleksandra, Sarasquete Maria Eugenia, Dudzi?ski Marek, Jurczyszyn Artur, Druzd-Sitek Agnieszka, Kruszewski Marcin, Subocz Edyta, Petrini Mario, Iskierka-Ja?d?ewska Elzbieta, Ra?ny Malgorzata, Szombath Gergely, Marques Herlander, Zawirska Daria, Chraniuk Dominik, Halka Janusz, Hove Jacobsen Svend Erik, Mazur Grzegorz, Sanz Ramón García, Dumontet Charles, Moreno Victor, St?pie? Anna, Beider Katia, Pelosini Matteo, Reis Rui Manuel, Krawczyk-Kulis Malgorzata, Rymko Marcin, Avet-Loiseau Hervé, Lesueur Fabienne, Grz??ko Norbert, Ostrovsky Olga, Jamroziak Krzysztof, Vangsted Annette J, Jerez Andrés, Tomczak Waldemar, Zaucha Jan Maciej, Kadar Katalin, Pérez Juan Sainz, Nagler Arnon, Landi Stefano, Gemignani Federica, Canzian Federi |
[Investigation of CNTF, COMT, DDR1, DISC1, DRD2, DRD3, and DTNBP1 candidate genes in schizophrenia: Results from the Hungarian SCHIZOBANK Consortium]. Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology 2016 Dec 18 (4): 181-187. Benkovits Judit, Magyarosi Szilvia, Pulay Attila J, Makkos Zoltan, Egerhazi Aniko, Balogh Nora, Almos Peter, Liko Istvan, Schizobank Consortium Hungarian, Nemeth Gyorgy, Molnar Judit Maria, Nagy Laszlo, Rethelyi Janos |
The prognostic effects of somatic mutations in ER-positive breast cancer. Nature communications 2018 Sep 9 (1): 3476. Griffith Obi L, Spies Nicholas C, Anurag Meenakshi, Griffith Malachi, Luo Jingqin, Tu Dongsheng, Yeo Belinda, Kunisaki Jason, Miller Christopher A, Krysiak Kilannin, Hundal Jasreet, Ainscough Benjamin J, Skidmore Zachary L, Campbell Katie, Kumar Runjun, Fronick Catrina, Cook Lisa, Snider Jacqueline E, Davies Sherri, Kavuri Shyam M, Chang Eric C, Magrini Vincent, Larson David E, Fulton Robert S, Liu Shuzhen, Leung Samuel, Voduc David, Bose Ron, Dowsett Mitch, Wilson Richard K, Nielsen Torsten O, Mardis Elaine R, Ellis Matthew |
Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.
Journal of molecular medicine (Berlin, Germany) 2018 Jun . Witten Anika, Bolbrinker Juliane, Barysenka Andrei, Huber Matthias, Rühle Frank, Nowak-Göttl Ulrike, Garbe Edeltraut, Kreutz Reinhold, Stoll Moni |
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Journal of the American Society of Nephrology : JASN 2019 Sep . Salem Rany M, Todd Jennifer N, Sandholm Niina, Cole Joanne B, Chen Wei-Min, Andrews Darrell, Pezzolesi Marcus G, McKeigue Paul M, Hiraki Linda T, Qiu Chengxiang, Nair Viji, Di Liao Chen, Cao Jing Jing, Valo Erkka, Onengut-Gumuscu Suna, Smiles Adam M, McGurnaghan Stuart J, Haukka Jani K, Harjutsalo Valma, Brennan Eoin P, van Zuydam Natalie, Ahlqvist Emma, Doyle Ross, Ahluwalia Tarunveer S, Lajer Maria, Hughes Maria F, Park Jihwan, Skupien Jan, Spiliopoulou Athina, Liu Andrew, Menon Rajasree, Boustany-Kari Carine M, Kang Hyun M, Nelson Robert G, Klein Ronald, Klein Barbara E, Lee Kristine E, Gao Xiaoyu, Mauer Michael, Maestroni Silvia, Caramori Maria Luiza, de Boer Ian H, Miller Rachel G, Guo Jingchuan, Boright Andrew P, Tregouet David, Gyorgy Beata, Snell-Bergeon Janet K, Maahs David M, Bull Shelley B, Canty Angelo J, Palmer Colin N A, Stechemesser Lars, Paulweber Bernhard, Weitgasser Raimund, Sokolovska Jelizaveta, Rov?te Vita, P?r?gs Valdis, Prakapiene Edita, Radzeviciene Lina, Verkauskiene Rasa, Panduru Nicolae Mircea, Groop Leif C, McCarthy Mark I, Gu Harvest F, Möllsten Anna, Falhammar Henrik, Brismar Kerstin, Martin Finian, Rossing Peter, Costacou Tina, Zerbini Gianpaolo, Marre Michel, Hadjadj Samy, McKnight Amy J, Forsblom Carol, McKay Gareth, Godson Catherine, Maxwell A Peter, Kretzler Matthias, Susztak Katalin, Colhoun Helen M, Krolewski Andrzej, Paterson Andrew D, Groop Per-Henrik, Rich Stephen S, Hirschhorn Joel N, Florez Jose C, |
CDH1 and DDR1 common variants confer risk to vitiligo and autoimmune comorbidities. Gene 2019 Mar 700 17-22. Almasi-Nasrabadi Mina, Amoli Mahsa M, Robati Reza M, Rajabi Fateme, Ghalamkarpour Fariba, Gauthier Yv |
Do age-related macular degeneration genes show association with keratoconus? Eye and vision (London, England) 2019 6 38. Cao Ke, Sahebjada Srujana, Richardson Andrea J, Baird Paul |
Discoidin domain receptor 1 gene variants are associated with decreased white matter fractional anisotropy and decreased processing speed in schizophrenia. Journal of psychiatric research 2019 1 110 74-82. Gas Cinta, Canales-Rodríguez Erick Jorge, Radua Joaquim, Abasolo Nerea, Cortés Maria José, Salvadó Ester, Muntané Gerard, Alemán-Gómez Yasser, Julià Toni, Marsal Sara, Sanjuan Julio, Guitart Miriam, Costas Javier, Martorell Lourdes, Pomarol-Clotet Edith, Vilella Elisab |
Fine mapping of the major histocompatibility complex (MHC) in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suggests involvement of both HLA class I and class II loci. Brain, behavior, and immunity 2021 Aug 98 101-109. Hajdarevic Riad, Lande Asgeir, Rekeland Ingrid, Rydland Anne, Strand Elin B, Sosa Daisy D, Creary Lisa E, Mella Olav, Egeland Torstein, Saugstad Ola D, Fluge Øystein, Lie Benedicte A, Viken Marte |
Coexpression of the discoidin domain receptor 1 gene with oligodendrocyte-related and schizophrenia risk genes in the developing and adult human brain. Brain and behavior 2021 7 11 (8): e2309. Muntané Gerard, Chillida Marc, Aranda Selena, Navarro Arcadi, Vilella Elisab |
Association between Interferon-Lambda-3 rs12979860, TLL1 rs17047200 and DDR1 rs4618569 Variant Polymorphisms with the Course and Outcome of SARS-CoV-2 Patients. Genes 2021 05 12 (6): . Agwa Sara H A, Kamel Marwa Mostafa, Elghazaly Hesham, Abd Elsamee Aya M, Hafez Hala, Girgis Samia Abdo, Ezz Elarab Hoda, Ebeid Fatma S E, Sayed Safa Matbouly, Sherif Lina, Matboli Mar |
Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder.
Pharmaceuticals (Basel, Switzerland) 2022 Jan 15 (2): . Almandil Noor B, AlSulaiman Abdulla, Aldakeel Sumayh A, Alkuroud Deem N, Aljofi Halah Egal, Alzahrani Safah, Al-Mana Aishah, Alfuraih Asma A, Alabdali Majed, Alkhamis Fahd A, AbdulAzeez Sayed, Borgio J Franc |
Cross-sectional and longitudinal assessment of the association between DDR1 variants and processing speed in patients with early psychosis and healthy controls. Journal of psychiatric research 2022 12 158 49-55. Gas Cinta, Ayesa-Arriola Rosa, Vázquez-Bourgon Javier, Crespo-Facorro Benedicto, García-Gavilán Jesús, Labad Javier, Martorell Lourdes, Muntané Gerard, Sanchez-Gistau Vanessa, Vilella Elisab |
Albuminuria-Related Genetic Biomarkers: Replication and Predictive Evaluation in Individuals with and without Diabetes from the UK Biobank. International journal of molecular sciences 2023 7 24 (13): . Marisa Cañadas-Garre, Andrew T Kunzmann, Kerry Anderson, Eoin P Brennan, Ross Doyle, Christopher C Patterson, Catherine Godson, Alexander P Maxwell, Amy Jayne McKnig |
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- Page last updated:Apr 22, 2024
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