Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: LMX1B[original query] |
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Phenotype severity and genetic variation at the disease locus: an investigation of nail dysplasia in the nail patella syndrome. Annals of human genetics 2005 1 69 (Pt 1): 1-8. Dunston J A, Lin S, Park J W, Malbroux M, McIntosh |
Association analysis of 15 polymorphisms within 10 candidate genes for antisocial behavioural traits. Psychiatric genetics 2007 Oct 17 (5): 299-303. Prichard Zoë M, Jorm Anthony F, Mackinnon Andrew, Easteal Sim |
The transcription factor PITX3 is associated with sporadic Parkinson's disease. Neurobiology of aging 2009 May 30 (5): 731-8. Fuchs Julia, Mueller Jakob C, Lichtner Peter, Schulte Claudia, Munz Marita, Berg Daniela, Wüllner Ullrich, Illig Thomas, Sharma Manu, Gasser Thom |
Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes. Investigative ophthalmology & visual science 2009 Apr 50 (4): 1522-30. Park Soo, Jamshidi Yalda, Vaideanu Daniela, Bitner-Glindzicz Maria, Fraser Scott, Sowden Jane |
Do polymorphisms in transcription factors LMX1A and LMX1B influence the risk for Parkinson's disease? Journal of neural transmission (Vienna, Austria : 1996) 2009 Mar 116 (3): 333-8. Bergman Olle, Håkansson Anna, Westberg Lars, Belin Andrea Carmine, Sydow Olof, Olson Lars, Holmberg Björn, Fratiglioni Laura, Bäckman Lars, Eriksson Elias, Nissbrandt Ha |
Preliminary evidence that polymorphisms in dopamine-related transcription factors LMX1A, LMX1B and PITX3 are associated with schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry 2010 Aug 34 (6): 1094-7. Bergman Olle, Westberg Lars, Nilsson Lars-Göran, Adolfsson Rolf, Eriksson Eli |
Association of transcription factor gene LMX1B with autism. PloS one 2011 6 (8): e23738. Thanseem Ismail, Nakamura Kazuhiko, Anitha Ayyappan, Suda Shiro, Yamada Kazuo, Iwayama Yoshimi, Toyota Tomoko, Tsujii Masatsugu, Iwata Yasuhide, Suzuki Katsuaki, Matsuzaki Hideo, Iwata Keiko, Sugiyama Toshiro, Yoshikawa Takeo, Mori Nor |
SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. Molecular vision 2012 18 1629-39. Chen Li Jia, Tam Pancy O S, Leung Dexter Y L, Fan Alex H, Zhang Mingzhi, Tham Clement C Y, Chiang Sylvia W Y, Fan Bao Jian, Wang Ningli, Pang Chi P |
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.
Human molecular genetics 2015 Nov . Felix Janine F, Bradfield Jonathan P, Monnereau Claire, van der Valk Ralf J P, Stergiakouli Evie, Chesi Alessandra, Gaillard Romy, Feenstra Bjarke, Thiering Elisabeth, Kreiner-Møller Eskil, Mahajan Anubha, Pitkänen Niina, Joro Raimo, Cavadino Alana, Huikari Ville, Franks Steve, Groen-Blokhuis Maria M, Cousminer Diana L, Marsh Julie A, Lehtimäki Terho, Curtin John A, Vioque Jesus, Ahluwalia Tarunveer S, Myhre Ronny, Price Thomas S, Vilor-Tejedor Natalia, Yengo Loïc, Grarup Niels, Ntalla Ioanna, Ang Wei, Atalay Mustafa, Bisgaard Hans, Blakemore Alexandra I, Bonnefond Amelie, Carstensen Lisbeth, , , Eriksson Johan, Flexeder Claudia, Franke Lude, Geller Frank, Geserick Mandy, Hartikainen Anna-Liisa, Haworth Claire M A, Hirschhorn Joel N, Hofman Albert, Holm Jens-Christian, Horikoshi Momoko, Hottenga Jouke Jan, Huang Jinyan, Kadarmideen Haja N, Kähönen Mika, Kiess Wieland, Lakka Hanna-Maaria, Lakka Timo A, Lewin Alexandra M, Liang Liming, Lyytikäinen Leo-Pekka, Ma Baoshan, Magnus Per, McCormack Shana E, McMahon George, Mentch Frank D, Middeldorp Christel M, Murray Clare S, Pahkala Katja, Pers Tune H, Pfäffle Roland, Postma Dirkje S, Power Christine, Simpson Angela, Sengpiel Verena, Tiesler Carla M T, Torrent Maties, Uitterlinden André G, van Meurs Joyce B, Vinding Rebecca, Waage Johannes, Wardle Jane, Zeggini Eleftheria, Zemel Babette S, Dedoussis George V, Pedersen Oluf, Froguel Philippe, Sunyer Jordi, Plomin Robert, Jacobsson Bo, Hansen Torben, Gonzalez Juan R, Custovic Adnan, Raitakari Olli T, Pennell Craig E, Widén Elisabeth, Boomsma Dorret I, Koppelman Gerard H, Sebert Sylvain, Järvelin Marjo-Riitta, Hyppönen Elina, McCarthy Mark I, Lindi Virpi, Harri Niinikoski, Körner Antje, Bønnelykke Klaus, Heinrich Joachim, Melbye Mads, Rivadeneira Fernando, Hakonarson Hakon, Ring Susan M, Smith George Davey, Sørensen Thorkild I A, Timpson Nicholas J, Grant Struan F A, Jaddoe Vincent W V, , |
Influence of genetic variants associated with body mass index on eating behavior in childhood. Obesity (Silver Spring, Md.) 2017 Feb . Monnereau Claire, Jansen Pauline W, Tiemeier Henning, Jaddoe Vincent W V, Felix Janine |
Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93. Pediatric nephrology (Berlin, Germany) 2018 Jun . Bezdí?ka Martin, Štolbová Šárka, Seeman Tomáš, Cinek Ond?ej, Malina Michal, Šimánková Nad?žda, Pr?hová Št?pánka, Zieg Jak |
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
Nature communications 2018 Jun 9 (1): 2278. Choquet Hélène, Paylakhi Seyyedhassan, Kneeland Stephen C, Thai Khanh K, Hoffmann Thomas J, Yin Jie, Kvale Mark N, Banda Yambazi, Tolman Nicholas G, Williams Pete A, Schaefer Catherine, Melles Ronald B, Risch Neil, John Simon W M, Nair K Saidas, Jorgenson Er |
Genome-wide association analyses identify new loci influencing intraocular pressure.
Human molecular genetics 2018 Mar . Gao X Raymond, Huang Hua, Nannini Drew R, Fan Fangda, Kim Heej |
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.
Scientific reports 2018 Feb 8 (1): 3124. Gharahkhani Puya, Burdon Kathryn P, Cooke Bailey Jessica N, Hewitt Alex W, Law Matthew H, Pasquale Louis R, Kang Jae H, Haines Jonathan L, Souzeau Emmanuelle, Zhou Tiger, Siggs Owen M, Landers John, Awadalla Mona, Sharma Shiwani, Mills Richard A, Ridge Bronwyn, Lynn David, Casson Robert, Graham Stuart L, Goldberg Ivan, White Andrew, Healey Paul R, Grigg John, Lawlor Mitchell, Mitchell Paul, Ruddle Jonathan, Coote Michael, Walland Mark, Best Stephen, Vincent Andrea, Gale Jesse, RadfordSmith Graham, Whiteman David C, Montgomery Grant W, Martin Nicholas G, Mackey David A, Wiggs Janey L, MacGregor Stuart, Craig Jamie E, |
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.
Human molecular genetics 2018 Feb . Shiga Yukihiro, Akiyama Masato, Nishiguchi Koji M, Sato Kota, Shimozawa Nobuhiro, Takahashi Atsushi, Momozawa Yukihide, Hirata Makoto, Matsuda Koichi, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Oze Isao, Mikami Haruo, Naito Mariko, Wakai Kenji, Yoshikawa Munemitsu, Miyake Masahiro, Yamashiro Kenji, , Kashiwagi Kenji, Iwata Takeshi, Mabuchi Fumihiko, Takamoto Mitsuko, Ozaki Mineo, Kawase Kazuhide, Aihara Makoto, Araie Makoto, Yamamoto Tetsuya, Kiuchi Yoshiaki, Nakamura Makoto, Ikeda Yasuhiro, Sonoda Koh-Hei, Ishibashi Tatsuro, Nitta Koji, Iwase Aiko, Shirato Shiroaki, Oka Yoshitaka, Satoh Mamoru, Sasaki Makoto, Fuse Nobuo, Suzuki Yoichi, Cheng Ching-Yu, Khor Chiea Chuen, Baskaran Mani, Perera Shamira, Aung Tin, Vithana Eranga N, Cooke Bailey Jessica N, Kang Jae H, Pasquale Louis R, Haines Jonathan L, , Wiggs Janey L, Burdon Kathryn P, Gharahkhani Puya, Hewitt Alex W, Mackey David A, MacGregor Stuart, Craig Jamie E, Allingham R Rand, Hauser Micheal, Ashaye Adeyinka, Budenz Donald L, Akafo Stephan, Williams Susan E I, Kamatani Yoichiro, Nakazawa Toru, Kubo Michia |
A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
Assessing the Role of 98 Established Loci for BMI in American Indians. Obesity (Silver Spring, Md.) 2019 Mar . Muller Yunhua L, Hanson Robert L, Piaggi Paolo, Chen Peng, Wiessner Gregory, Okani Chidinma, Skelton Graham, Kobes Sayuko, Hsueh Wen-Chi, Knowler William C, Bogardus Clifton, Baier Leslie |
An Exome Sequencing Study of 10 Families with IgA Nephropathy. Nephron 2019 Dec 1-12. Stapleton Caragh P, Kennedy Claire, Fennelly Neil K, Murray Susan L, Connaughton Dervla M, Dorman Anthony M, Doyle Brendan, Cavalleri Gianpiero L, Conlon Peter |
LMX1B rs10733682 Polymorphism Interacts with Macronutrients, Dietary Patterns on the Risk of Obesity in Han Chinese Girls. Nutrients 2020 Apr 12 (5): . Zhu Qi, Xue Kun, Guo Hong Wei, Yang Yu Hu |
Obesity Genes and Weight Loss During Lifestyle Intervention in Children With Obesity. JAMA pediatrics 2020 Dec e205142. Heitkamp Melanie, Siegrist Monika, Molnos Sophie, Brandmaier Stefan, Wahl Simone, Langhof Helmut, Grallert Harald, Halle Mart |
Effect of 15 BMI-Associated Polymorphisms, Reported for Europeans, across Ethnicities and Degrees of Amerindian Ancestry in Mexican Children. International journal of molecular sciences 2020 Jan 21 (2): . Costa-Urrutia Paula, Abud Carolina, Franco-Trecu Valentina, Colistro Valentina, Rodríguez-Arellano Martha Eunice, Alvarez-Fariña Rafael, Acuña Alonso Víctor, Bertoni Bernardo, Granados Jul |
Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome. Molecular biology reports 2021 Sep . Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya |
Association analysis of variants rs35934224 in TXNRD2 and rs6478746 in LMX1B in primary angle-closure and pseudoexfoliation glaucoma. European journal of ophthalmology 2021 8 32 (4): 2249-2258. Kondkar Altaf A, Sultan Tahira, Alobaidan Abdullah S, Azad Taif A, Osman Essam A, Almobarak Faisal A, Lobo Glenn P, Al-Obeidan Saleh |
Lack of Association Between Polymorphisms in TXNRD2 and LMX1B and Primary Open-Angle Glaucoma in a Saudi Cohort. Frontiers in genetics 2021 12 690780. Kondkar Altaf A, Azad Taif A, Alobaidan Abdullah S, Sultan Tahira, Osman Essam A, Almobarak Faisal A, Lobo Glenn P, Al-Obeidan Saleh |
Genetic Interactions with Intrauterine Diabetes Exposure in Relation to Obesity: The EPOCH and Project Viva Studies. Pediatric reports 2021 Jun 13 (2): 279-288. Stanislawski Maggie A, Litkowski Elizabeth, Fore Ruby, Rifas-Shiman Sheryl L, Oken Emily, Hivert Marie-France, Lange Ethan M, Lange Leslie A, Dabelea Dana, Raghavan Sridhar |
Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.
Cancers 2021 Feb 13 (4): . Adjei Araba A, Lopez Camden L, Schaid Daniel J, Sloan Jeff A, Le-Rademacher Jennifer G, Loprinzi Charles L, Norman Aaron D, Olson Janet E, Couch Fergus J, Beutler Andreas S, Vachon Celine M, Ruddy Kathryn |
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure. Kidney international reports 2023 10 8 (10): 2126-2135. Yishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, Orly Haskin, Efrat Ben-Shalom, Hadas Shasha Lavsky, Oded Volovelsky, Shrikant Mane, Dror Ben-Ruby, Guy Chowers, Karl Skorecki, Yael Borovitz, Maayan Kagan, Nofar Mor, Yulia Khavkin, Shimrit Tzvi-Behr, Shirley Pollack, Moran Plonsky Toder, Michael Geylis, Aviad Schnapp, Rachel Becker-Cohen, Irith Weissman, Ruth Schreiber, Miriam Davidovits, Yaacov Frishberg, Daniella Magen, Ortal Barel, Asaf Vivan |
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences 2024 1 . Fulya Akçimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Trayn |
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