Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: GRB10[original query] |
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GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients. Neuroscience letters 2009 Oct 463 (3): 172-5. Zhang Yu, Zheng Lan, Zhang Ting, Wang Ying, Xiao Qin, Fei Qin-Zhou, Cui Pei-Jing, Cao Li, Chen Sheng- |
GIGYF2 mutations are not a frequent cause of familial Parkinson's disease. Parkinsonism & related disorders 2009 Nov 15 (9): 703-5. Di Fonzo Alessio, Fabrizio Edito, Thomas Astrid, Fincati Emiliana, Marconi Roberto, Tinazzi Michele, Breedveld Guido J, Simons Erik J, Chien Hsin F, Ferreira Joaquim J, Horstink Martin W, Abbruzzese Giovanni, Borroni Barbara, Cossu Giovanni, Dalla Libera Alessio, Fabbrini Giovanni, Guidi Marco, De Mari Michele, Lopiano Leonardo, Martignoni Emilia, Marini Paolo, Onofrj Marco, Padovani Alessandro, Stocchi Fabrizio, Toni Vincenzo, Sampaio Cristina, Barbosa Egberto R, Meco Giuseppe, , Oostra Ben A, Bonifati Vincen |
GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients. Neuroscience letters 2009 May 454 (3): 209-11. Guo Yi, Jankovic Joseph, Zhu Shaihong, Le Weidong, Song Zhi, Xie Wenjie, Liao Daoguang, Yang Huarong, Deng H |
PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease. Parkinsonism & related disorders 2009 Aug 15 (7): 532-4. Zimprich Alexander, Schulte Claudia, Reinthaler Eva, Haubenberger Dietrich, Balzar Jörg, Lichtner Peter, El Tawil Salwa, Edris S, Foki Thomas, Pirker Walter, Katzenschlager Regina, Daniel Gerhard, Brücke Thomas, Auff Eduard, Gasser Thom |
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population. Neurobiology of aging 2009 Mar . Meeus B, Nuytemans K, Crosiers D, Engelborghs S, Pals P, Pickut B, Peeters K, Mattheijssens M, Corsmit E, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C |
Follow-up study of the GIGYF2 gene in French families with Parkinson's disease. Neurobiology of aging 2010 Jun 31 (6): 1069-71; discussion 1072-4. Lesage Suzanne, Condroyer Christel, Lohman Ebba, Troiano André, Tison François, Viallet François, Damier Philippe, Tranchant Christine, Vidhaillet Marie, Ouvrard-Hernandez Anne-Marie, Dürr Alexandra, Brice Alexis, |
[Occurrence of GRB10 (+11275G > A) polymorphism in Hungarian population and its relationship to glucose metabolism]. Orvosi hetilap 2009 Oct 150 (40): 1845-51. Vitai Márta, Buday Barbara, Kulcsár Eniko, Literáti-Nagy Botond, Vecsei Istvánné, Bezzegh Katalin, Péterfai Eva, Kurucz István, Korányi Lász |
No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients. Neuroscience letters 2010 (3): 245-8. Li Lin, Funayama Manabu, Tomiyama Hiroyuki, Li Yuanzhe, Yoshino Hiroyo, Sasaki Ryogen, Kokubo Yasumasa, Kuzuhara Shigeki, Mizuno Yoshikuni, Hattori Nobuta |
Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population. Neuroscience letters 2010 Apr 473 (2): 131-5. Wang Lei, Guo Ji-feng, Zhang Wen-wen, Xu Qian, Zuo Xing, Shi Chang-he, Luo Lin-zi, Liu Jia, Hu Liang, Hu Ya-cen, She Lu, Jiang Hong, Yan Xin-xiang, Xia Kun, Pan Qian, Tang Bei-s |
The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese population. Parkinsonism & related disorders 2009 Dec . Cao L, Zhang T, Zheng L, Wang Y, Wang G, Zhang J, Fei Q Z, Cui P J, Wang X J, Ma J F, Xiao Q, Chen S |
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene. Neurobiology of aging 2011 Nov 32 (11): 1994-2005. Guella Ilaria, Pistocchi Anna, Asselta Rosanna, Rimoldi Valeria, Ghilardi Anna, Sironi Francesca, Trotta Luca, Primignani Paola, Zini Michela, Zecchinelli Anna, Coviello Domenico, Pezzoli Gianni, Del Giacco Luca, Duga Stefano, Goldwurm Stefa |
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
PLoS genetics 2011 Jul 7 (7): e1002178. Gorlova Olga, Martin Jose-Ezequiel, Rueda Blanca, Koeleman Bobby P C, Ying Jun, Teruel Maria, Diaz-Gallo Lina-Marcela, Broen Jasper C, Vonk Madelon C, Simeon Carmen P, Alizadeh Behrooz Z, Coenen Marieke J H, Voskuyl Alexandre E, Schuerwegh Annemie J, van Riel Piet L C M, Vanthuyne Marie, van 't Slot Ruben, Italiaander Annet, Ophoff Roel A, Hunzelmann Nicolas, Fonollosa Vicente, Ortego-Centeno Norberto, González-Gay Miguel A, García-Hernández Francisco J, González-Escribano María F, Airo Paolo, van Laar Jacob, Worthington Jane, Hesselstrand Roger, Smith Vanessa, de Keyser Filip, Houssiau Fredric, Chee Meng May, Madhok Rajan, Shiels Paul G, Westhovens Rene, Kreuter Alexander, de Baere Elfride, Witte Torsten, Padyukov Leonid, Nordin Annika, Scorza Raffaella, Lunardi Claudio, Lie Benedicte A, Hoffmann-Vold Anna-Maria, Palm Oyvind, García de la Peña Paloma, Carreira Patricia, , Varga John, Hinchcliff Monique, Lee Annette T, Gourh Pravitt, Amos Christopher I, Wigley Frederick M, Hummers Laura K, Nelson J Lee, Riemekasten Gabriella, Herrick Ariane, Beretta Lorenzo, Fonseca Carmen, Denton Christopher P, Gregersen Peter K, Agarwal Sandeep, Assassi Shervin, Tan Filemon K, Arnett Frank C, Radstake Timothy R D J, Mayes Maureen D, Martin Javi |
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2013 Sep 169 (3): 277-89. Clayton P, Chatelain P, Tatò L, Yoo H W, Ambler G R, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier |
Five linkage regions each harbor multiple type 2 diabetes genes in the African American subset of the GENNID Study. Journal of human genetics 2013 Jun 58 (6): 378-83. Hasstedt Sandra J, Highland Heather M, Elbein Steven C, Hanis Craig L, Das Swapan K, |
Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA. Human genetics 2014 May 133 (5): 481-97. Earp Madalene A, Kelemen Linda E, Magliocco Anthony M, Swenerton Kenneth D, Chenevix-Trench Georgia, , , Lu Yi, Hein Alexander, Ekici Arif B, Beckmann Matthias W, Fasching Peter A, Lambrechts Diether, Despierre Evelyn, Vergote Ignace, Lambrechts Sandrina, Doherty Jennifer A, Rossing Mary Anne, Chang-Claude Jenny, Rudolph Anja, Friel Grace, Moysich Kirsten B, Odunsi Kunle, Sucheston-Campbell Lara, Lurie Galina, Goodman Marc T, Carney Michael E, Thompson Pamela J, Runnebaum Ingo B, Dürst Matthias, Hillemanns Peter, Dörk Thilo, Antonenkova Natalia, Bogdanova Natalia, Leminen Arto, Nevanlinna Heli, Pelttari Liisa M, Butzow Ralf, Bunker Clareann H, Modugno Francesmary, Edwards Robert P, Ness Roberta B, du Bois Andreas, Heitz Florian, Schwaab Ira, Harter Philipp, Karlan Beth Y, Walsh Christine, Lester Jenny, Jensen Allan, Kjær Susanne K, Høgdall Claus K, Høgdall Estrid, Lundvall Lene, Sellers Thomas A, Fridley Brooke L, Goode Ellen L, Cunningham Julie M, Vierkant Robert A, Giles Graham G, Baglietto Laura, Severi Gianluca, Southey Melissa C, Liang Dong, Wu Xifeng, Lu Karen, Hildebrandt Michelle A T, Levine Douglas A, Bisogna Maria, Schildkraut Joellen M, Iversen Edwin S, Weber Rachel Palmieri, Berchuck Andrew, Cramer Daniel W, Terry Kathryn L, Poole Elizabeth M, Tworoger Shelley S, Bandera Elisa V, Chandran Urmila, Orlow Irene, Olson Sara H, Wik Elisabeth, Salvesen Helga B, Bjorge Line, Halle Mari K, van Altena Anne M, Aben Katja K H, Kiemeney Lambertus A, Massuger Leon F A G, Pejovic Tanja, Bean Yukie T, Cybulski Cezary, Gronwald Jacek, Lubinski Jan, Wentzensen Nicolas, Brinton Louise A, Lissowska Jolanta, Garcia-Closas Montserrat, Dicks Ed, Dennis Joe, Easton Douglas F, Song Honglin, Tyrer Jonathan P, Pharoah Paul D P, Eccles Diana, Campbell Ian G, Whittemore Alice S, McGuire Valerie, Sieh Weiva, Rothstein Joseph H, Flanagan James M, Paul James, Brown Robert, Phelan Catherine M, Risch Harvey A, McLaughlin John R, Narod Steven A, Ziogas Argyrios, Anton-Culver Hoda, Gentry-Maharaj Aleksandra, Menon Usha, Gayther Simon A, Ramus Susan J, Wu Anna H, Pearce Celeste L, Pike Malcolm C, Dansonka-Mieszkowska Agnieszka, Rzepecka Iwona K, Szafron Lukasz M, Kupryjanczyk Jolanta, Cook Linda S, Le Nhu D, Brooks-Wilson Angela, |
A genetic locus in 7p12.2 associated with treatment resistant schizophrenia.
Schizophrenia research 2014 Nov 159 (2-3): 333-9. Li Jiang, Meltzer Herbert |
Association of the intronic polymorphism rs12540874 A>G of the GRB10 gene with high birth weight. Early human development 2014 Oct 90 (10): 545-8. González-Renteria Siblie Marbey, Sosa-Macías Martha, Rodríguez-Moran Martha, Chairez-Hernández Isaías, Lares-Aseff Ismael A, Guerrero-Romero Fernando, Galaviz-Hernández Carl |
A central role for GRB10 in regulation of islet function in man.
PLoS genetics 2014 Apr 10 (4): e1004235. Prokopenko Inga, Poon Wenny, Mägi Reedik, Prasad B Rashmi, Salehi S Albert, Almgren Peter, Osmark Peter, Bouatia-Naji Nabila, Wierup Nils, Fall Tove, Stancáková Alena, Barker Adam, Lagou Vasiliki, Osmond Clive, Xie Weijia, Lahti Jari, Jackson Anne U, Cheng Yu-Ching, Liu Jie, O'Connell Jeffrey R, Blomstedt Paul A, Fadista Joao, Alkayyali Sami, Dayeh Tasnim, Ahlqvist Emma, Taneera Jalal, Lecoeur Cecile, Kumar Ashish, Hansson Ola, Hansson Karin, Voight Benjamin F, Kang Hyun Min, Levy-Marchal Claire, Vatin Vincent, Palotie Aarno, Syvänen Ann-Christine, Mari Andrea, Weedon Michael N, Loos Ruth J F, Ong Ken K, Nilsson Peter, Isomaa Bo, Tuomi Tiinamaija, Wareham Nicholas J, Stumvoll Michael, Widen Elisabeth, Lakka Timo A, Langenberg Claudia, Tönjes Anke, Rauramaa Rainer, Kuusisto Johanna, Frayling Timothy M, Froguel Philippe, Walker Mark, Eriksson Johan G, Ling Charlotte, Kovacs Peter, Ingelsson Erik, McCarthy Mark I, Shuldiner Alan R, Silver Kristi D, Laakso Markku, Groop Leif, Lyssenko Valeri |
Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets. PLoS genetics 2014 Nov 10 (11): e1004735. Olsson Anders H, Volkov Petr, Bacos Karl, Dayeh Tasnim, Hall Elin, Nilsson Emma A, Ladenvall Claes, Rönn Tina, Ling Charlot |
Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease. Journal of Alzheimer's disease : JAD 2015 Jan 44 (3): 989-94. Chaudhry Mamoonah, Wang Xingbin, Bamne Mikhil N, Hasnain Shahida, Demirci F Yesim, Lopez Oscar L, Kamboh M Ily |
Meta-analyses of seven GIGYF2 polymorphisms with Parkinson's disease. Biomedical reports 2014 Nov 2 (6): 886-892. Dai Dongjun, Wang Yunliang, Zhou Xingyu, Tao Jianmin, Jiang Danjie, Zhou Hanlin, Jiang Yi, Pan Guanghui, Ru Ping, Ji Huihui, Li Jinfeng, Zhang Yuzheng, Yin Honglei, Xu Mingqing, Duan Shiw |
Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study. European journal of endocrinology 2016 Dec 175 (6): 633-643. Stevens Adam, Murray Philip, Wojcik Jerome, Raelson John, Koledova Ekaterina, Chatelain Pierre, Clayton Peter, |
Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study. PloS one 2016 11 (4): e0152107. Sohani Zahra N, Anand Sonia S, Robiou-du-Pont Sebastien, Morrison Katherine M, McDonald Sarah D, Atkinson Stephanie A, Teo Koon K, Meyre Dav |
Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57. BMC medical genetics 2016 17 (1): 29. Bak Mads, Boonen Susanne E, Dahl Christina, Hahnemann Johanne M D, Mackay Deborah J D G, Tümer Zeynep, Grønskov Karen, Temple I Karen, Guldberg Per, Tommerup Nie |
Genetic Polymorphisms as Predictive Markers of Response to Growth Hormone Therapy in Children with Growth Hormone Deficiency. Klinische Padiatrie 2017 Aug . Jung Anna Maria, Zenker Martin, Lißewski Christina, Schanze Denny, Wagenpfeil Stefan, Rohrer Tilman Robe |
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.
BMJ (Clinical research ed.) 2018 Aug 362 k3225. Trajanoska Katerina, Morris John A, Oei Ling, Zheng Hou-Feng, Evans David M, Kiel Douglas P, Ohlsson Claes, Richards J Brent, Rivadeneira Fernando, |
Probe-based association analysis identifies several deletions associated with average daily gain in beef cattle. BMC genomics 2019 1 20 (1): 31. Xu Lingyang, Yang Liu, Wang Lei, Zhu Bo, Chen Yan, Gao Huijiang, Gao Xue, Zhang Lupei, Liu George E, Li Jun |
Lifestyle mediates the role of nutrient-sensing pathways in cognitive aging: cellular and epidemiological evidence. Communications biology 2020 4 3 (1): 157. de Lucia Chiara, Murphy Tytus, Steves Claire J, Dobson Richard J B, Proitsi Petroula, Thuret Sandri |
GRB10 rs1800504 Polymorphism Is Associated With the Risk of Coronary Heart Disease in Patients With Type 2 Diabetes Mellitus. Frontiers in cardiovascular medicine 2021 10 8 728976. Yang Yang, Qiu Wentao, Meng Qian, Liu Mouze, Lin Weijie, Yang Haikui, Wang Ruiqi, Dong Jiamei, Yuan Ningning, Zhou Zhiling, He Fazho |
A genome-wide screen for resilient responses in growing pigs. Genetics, selection, evolution : GSE 2022 7 54 (1): 50. Laghouaouta Houda, Fraile Lorenzo, Suárez-Mesa Rafael, Ros-Freixedes Roger, Estany Joan, Pena Ramona Natac |
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- Page last updated:Apr 22, 2024
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