Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: PDE8B[original query] |
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Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.
American journal of human genetics 2008 Jun 82 (6): 1270-80. Arnaud-Lopez Lisette, Usala Gianluca, Ceresini Graziano, Mitchell Braxton D, Pilia Maria Grazia, Piras Maria Grazia, Sestu Natascia, Maschio Andrea, Busonero Fabio, Albai Giuseppe, Dei Mariano, Lai Sandra, Mulas Antonella, Crisponi Laura, Tanaka Toshiko, Bandinelli Stefania, Guralnik Jack M, Loi Angela, Balaci Lenuta, Sole Gabriella, Prinzis Alessia, Mariotti Stefano, Shuldiner Alan R, Cao Antonio, Schlessinger David, Uda Manuela, Abecasis Gonçalo R, Nagaraja Ramaiah, Sanna Serena, Naitza Silv |
Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes. European journal of endocrinology / European Federation of Endocrine Societies 2009 Jul 161 (1): 153-61. Bimpaki Eirini I, Nesterova Maria, Stratakis Constantine |
Phosphodiesterase 8B gene polymorphism is associated with subclinical hypothyroidism in pregnancy. The Journal of clinical endocrinology and metabolism 2009 Nov 94 (11): 4608-12. Shields Beverley M, Freathy Rachel M, Knight Bridget A, Hill Anita, Weedon Michael N, Frayling Timothy M, Hattersley Andrew T, Vaidya Bij |
Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.
Molecular psychiatry 2011 Sep 16 (9): 927-37, 881. Stein J L, Hibar D P, Madsen S K, Khamis M, McMahon K L, de Zubicaray G I, Hansell N K, Montgomery G W, Martin N G, Wright M J, Saykin A J, Jack C R, Weiner M W, Toga A W, Thompson P M, |
A large-scale association analysis of 68 thyroid hormone pathway genes with serum TSH and FT4 levels. European journal of endocrinology / European Federation of Endocrine Societies 2011 May 164 (5): 781-8. Medici Marco, van der Deure Wendy M, Verbiest Michael, Vermeulen Sita H, Hansen Pia S, Kiemeney Lambertus A, Hermus Ad R M M, Breteler Monique M, Hofman Albert, Hegedüs Laszlo, Kyvik Kirsten Ohm, den Heijer Martin, Uitterlinden André G, Visser Theo J, Peeters Robin |
A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement. European journal of endocrinology / European Federation of Endocrine Societies 2011 May 164 (5): 773-80. Taylor Peter N, Panicker Vijay, Sayers Adrian, Shields Beverley, Iqbal Ahmed, Bremner Alexandra P, Beilby John P, Leedman Peter J, Hattersley Andrew T, Vaidya Bijay, Frayling Timothy, Evans Jonathan, Tobias Jonathan H, Timpson Nicholas J, Walsh John P, Dayan Colin |
Impact of phosphodiesterase 8B gene rs4704397 variation on thyroid homeostasis in childhood obesity. European journal of endocrinology / European Federation of Endocrine Societies 2012 Feb 166 (2): 255-60. Grandone Anna, Perrone Laura, Cirillo Grazia, Di Sessa Anna, Corona Alberto Maria, Amato Alessandra, Cresta Nicoletta, Romano Tiziana, Miraglia del Giudice Emanue |
[Association analysis of PDE8B gene polymorphisms with the susceptibility to Hyperthyroxinemia in Chinese Han population]. Zhonghua yi xue za zhi 2012 Mar 92 (12): 801-5. Zhan Ming, Zhao Shuang-xia, Gu Zhao-hui, Guo Cui-cui, Song Zhi-yi, Song Huai-do |
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.
Human molecular genetics 2012 Jul 21 (14): 3275-82. Rawal Rajesh, Teumer Alexander, Völzke Henry, Wallaschofski Henri, Ittermann Till, Åsvold Bjørn O, Bjøro Trine, Greiser Karin H, Tiller Daniel, Werdan Karl, Meyer zu Schwabedissen Henriette E, Doering Angela, Illig Thomas, Gieger Christian, Meisinger Christa, Homuth Geo |
Novel associations for hypothyroidism include known autoimmune risk loci.
PloS one 2012 7 (4): e34442. Eriksson Nicholas, Tung Joyce Y, Kiefer Amy K, Hinds David A, Francke Uta, Mountain Joanna L, Do Chuong |
Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours. Clinical endocrinology 2012 Aug 77 (2): 195-9. Rothenbuhler Anya, Horvath Anelia, Libé Rossella, Faucz Fabio R, Fratticci Amato, Raffin Sanson Marie L, Vezzosi Delphine, Azevedo Monalisa, Levy Isaak, Almeida Madson Q, Lodish Maya, Nesterova Maria, Bertherat Jérôme, Stratakis Constantine |
Phosphodiesterase 8B gene polymorphism in women with recurrent miscarriage: a retrospective case control study. BMC medical genetics 2012 Dec 13 (1): 1. Granfors M, Karypidis H, Hosseini F, Skjöldebrand-Sparre L, Stavreus-Evers A, Bremme K, Landgren BM, Sundström-Poromaa I, Wikström AK, Akerud H |
The phosphodiesterase 8B gene rs4704397 is associated with thyroid function, risk of myocardial infarction, and body height: the Tromsø study. Thyroid : official journal of the American Thyroid Association 2014 Feb 24 (2): 215-22. Jorde Rolf, Schirmer Henrik, Wilsgaard Tom, Joakimsen Ragnar Martin, Mathiesen Ellisiv Bøgeberg, Njølstad Inger, Løchen Maja-Lisa, Figenschau Yngve, Svartberg Johan, Hutchinson Moira Strand, Kjærgaard Marie, Jørgensen Lone, Grimnes Gu |
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.
PLoS genetics 2013 9 (2): e1003266. Porcu Eleonora, Medici Marco, Pistis Giorgio, Volpato Claudia B, Wilson Scott G, Cappola Anne R, Bos Steffan D, Deelen Joris, den Heijer Martin, Freathy Rachel M, Lahti Jari, Liu Chunyu, Lopez Lorna M, Nolte Ilja M, O'Connell Jeffrey R, Tanaka Toshiko, Trompet Stella, Arnold Alice, Bandinelli Stefania, Beekman Marian, Böhringer Stefan, Brown Suzanne J, Buckley Brendan M, Camaschella Clara, de Craen Anton J M, Davies Gail, de Visser Marieke C H, Ford Ian, Forsen Tom, Frayling Timothy M, Fugazzola Laura, Gögele Martin, Hattersley Andrew T, Hermus Ad R, Hofman Albert, Houwing-Duistermaat Jeanine J, Jensen Richard A, Kajantie Eero, Kloppenburg Margreet, Lim Ee M, Masciullo Corrado, Mariotti Stefano, Minelli Cosetta, Mitchell Braxton D, Nagaraja Ramaiah, Netea-Maier Romana T, Palotie Aarno, Persani Luca, Piras Maria G, Psaty Bruce M, Räikkönen Katri, Richards J Brent, Rivadeneira Fernando, Sala Cinzia, Sabra Mona M, Sattar Naveed, Shields Beverley M, Soranzo Nicole, Starr John M, Stott David J, Sweep Fred C G J, Usala Gianluca, van der Klauw Melanie M, van Heemst Diana, van Mullem Alies, Vermeulen Sita H, Visser W Edward, Walsh John P, Westendorp Rudi G J, Widen Elisabeth, Zhai Guangju, Cucca Francesco, Deary Ian J, Eriksson Johan G, Ferrucci Luigi, Fox Caroline S, Jukema J Wouter, Kiemeney Lambertus A, Pramstaller Peter P, Schlessinger David, Shuldiner Alan R, Slagboom Eline P, Uitterlinden André G, Vaidya Bijay, Visser Theo J, Wolffenbuttel Bruce H R, Meulenbelt Ingrid, Rotter Jerome I, Spector Tim D, Hicks Andrew A, Toniolo Daniela, Sanna Serena, Peeters Robin P, Naitza Silv |
Genetic associations with neonatal thyroid-stimulating hormone levels. Pediatric research 2013 Jan . Alul FY, Shchelochkov OA, Berberich SL, Murray JC, Ryckman KK |
Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism. Journal of endocrinological investigation 2014 Feb 37 (2): 189-94. Agretti P, De Marco G, Di Cosmo C, Bagattini B, Ferrarini E, Montanelli L, Vitti P, Tonacchera |
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.
PloS one 2014 9 (12): e111301. Malinowski Jennifer R, Denny Joshua C, Bielinski Suzette J, Basford Melissa A, Bradford Yuki, Peissig Peggy L, Carrell David, Crosslin David R, Pathak Jyotishman, Rasmussen Luke, Pacheco Jennifer, Kho Abel, Newton Katherine M, Li Rongling, Kullo Iftikhar J, Chute Christopher G, Chisholm Rex L, Jarvik Gail P, Larson Eric B, McCarty Catherine A, Masys Daniel R, Roden Dan M, de Andrade Mariza, Ritchie Marylyn D, Crawford Dana |
Whole-genome sequence-based analysis of thyroid function.
Nature communications 2015 6 5681. Taylor Peter N, Porcu Eleonora, Chew Shelby, Campbell Purdey J, Traglia Michela, Brown Suzanne J, Mullin Benjamin H, Shihab Hashem A, Min Josine, Walter Klaudia, Memari Yasin, Huang Jie, Barnes Michael R, Beilby John P, Charoen Pimphen, Danecek Petr, Dudbridge Frank, Forgetta Vincenzo, Greenwood Celia, Grundberg Elin, Johnson Andrew D, Hui Jennie, Lim Ee M, McCarthy Shane, Muddyman Dawn, Panicker Vijay, Perry John R B, Bell Jordana T, Yuan Wei, Relton Caroline, Gaunt Tom, Schlessinger David, Abecasis Goncalo, Cucca Francesco, Surdulescu Gabriela L, Woltersdorf Wolfram, Zeggini Eleftheria, Zheng Hou-Feng, Toniolo Daniela, Dayan Colin M, Naitza Silvia, Walsh John P, Spector Tim, Davey Smith George, Durbin Richard, Richards J Brent, Sanna Serena, Soranzo Nicole, Timpson Nicholas J, Wilson Scott G, |
Genetic association study of phosphodiesterase 8B gene with subclinical hypothyroidism in pregnant women. Endocrine research 2015 Aug 1-5. Yang Shuai, Tao Jun, Zhang Junyu, Fan Jianxia, Qian Wei, Shu Kh |
Alterations of Phosphodiesterases in Adrenocortical Tumors. Frontiers in endocrinology 2016 7 111. Hannah-Shmouni Fady, Faucz Fabio R, Stratakis Constantine |
Replication confirms the association of loci in FOXE1, PDE8B, CAPZB and PDE10A with thyroid traits: a Genetics of Diabetes Audit and Research Tayside study (GoDARTS). Pharmacogenetics and genomics 2017 Jul . Soto-Pedre Enrique, Siddiqui Moneeza K, Doney Alex S, Palmer Colin N A, Pearson Ewan R, Leese Graham |
Association of established hypothyroidism-associated genetic variants with Hashimoto's thyroiditis. Journal of endocrinological investigation 2017 Apr . Bari? A, Br?i? L, Gra?an S, Torlak Lovri? V, Gunja?a I, Šimunac M, Brekalo M, Boban M, Polašek O, Barbali? M, Zemunik T, Punda A, Boraska Perica |
PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population. Neurobiology of aging 2018 May . Fan Tian-Sin, Wu Ruey-Meei, Lin Han-I, Cheng Chieh, Lin Chin-Hsi |
Transcriptome Analyses Identify a Metabolic Gene Signature Indicative of Dedifferentiation of Papillary Thyroid Cancer. The Journal of clinical endocrinology and metabolism 2019 Apr . Ma Ben, Jiang Hongyi, Wen Duo, Hu Jiaqian, Han Litao, Liu Wanlin, Xu Weibo, Shi Xiao, Wei Wenjun, Liao Tian, Wang Yulong, Lu Zhongwu, Wang Yu, Ji Qingh |
Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disorders. Parkinsonism & related disorders 2019 11 69 94-98. Ni Jie, Yi Xiaoping, Liu Zhen, Sun Weining, Yuan Yanchun, Yang Jie, Jiang Hong, Shen Lu, Tang Beisha, Liu Yunhai, Wang Junli |
A Polygenic Risk Score of Lipolysis-Increasing Alleles Determines Visceral Fat Mass and Proinsulin Conversion. The Journal of clinical endocrinology and metabolism 2019 Jan . Kempe-Teufel Daniela, Machicao Fausto, Machann Jürgen, Böhm Anja, Schick Fritz, Fritsche Andreas, Stefan Norbert, Hrab? de Angelis Martin, Häring Hans-Ulrich, Staiger Hara |
Phosphodiesterase 8B Polymorphism rs4704397 Is Associated with Infertility in Subclinical Hypothyroid Females: A Case-Control Study. International journal of fertility & sterility 2020 Jul 14 (2): 122-128. Mansuri Tabassum, Jadeja S Hahnawaz D, Singh Mala, Begum Rasheedunnisa, Robin Push |
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- Page last updated:Apr 22, 2024
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