Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and CNTNAP2[original query] |
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Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.
Human molecular genetics 2011 Apr 20 (7): 1456-66. Sharma Swarkar, Gao Xiaochong, Londono Douglas, Devroy Shonn E, Mauldin Kristen N, Frankel Jessica T, Brandon January M, Zhang Dongping, Li Quan-Zhen, Dobbs Matthew B, Gurnett Christina A, Grant Struan F A, Hakonarson Hakon, Dormans John P, Herring John A, Gordon Derek, Wise Carol |
| TARV: tree-based analysis of rare variants identifying risk modifying variants in CTNNA2 and CNTNAP2 for alcohol addiction. Genetic epidemiology 2014 Sep 38 (6): 552-9. Song Chi, Zhang Hepi |
| Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controls. Neurobiology of aging 2015 Feb 36 (2): 1105-9. Infante Jon, Prieto Carlos, Sierra María, Sánchez-Juan Pascual, González-Aramburu Isabel, Sánchez-Quintana Coro, Berciano José, Combarros Onofre, Sainz Jes |
| Lack of association between DSCAM gene polymorphisms and adolescent idiopathic scoliosis susceptibility in a Chinese Han population. Journal of back and musculoskeletal rehabilitation 2014 Nov . Wu Weifei, Zhu Zezhang, Mao Saihu, Qiu Xusheng, Qian Bangping, Liu Zhen, Qiu Yo |
| A candidate gene association study further corroborates involvement of contactin genes in autism. Molecular syndromology 2014 Aug 5 (5): 229-35. Poot Mart |
| Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
| A genome-wide association study of late-onset Alzheimer's disease in a Japanese population.
Psychiatric genetics 2015 Aug 25 (4): 139-46. Hirano Atsushi, Ohara Tomoyuki, Takahashi Atsushi, Aoki Masayuki, Fuyuno Yuta, Ashikawa Kyota, Morihara Takashi, Takeda Masatoshi, Kamino Kouzin, Oshima Etsuko, Okahisa Yuko, Shibata Nobuto, Arai Heii, Akatsu Hiroyasu, Ikeda Masashi, Iwata Nakao, Ninomiya Toshiharu, Monji Akira, Kitazono Takanari, Kiyohara Yutaka, Kubo Michiaki, Kanba Shigeno |
| First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.
PloS one 2015 10 (3): e0119333. Anderson Denise, Cordell Heather J, Fakiola Michaela, Francis Richard W, Syn Genevieve, Scaman Elizabeth S H, Davis Elizabeth, Miles Simon J, McLeay Toby, Jamieson Sarra E, Blackwell Jenefer |
| Copy number variations in a population-based study of Charcot-Marie-Tooth disease. BioMed research international 2015 2015 960404. Høyer Helle, Braathen Geir J, Eek Anette K, Nordang Gry B N, Skjelbred Camilla F, Russell Michael |
| Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
| A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus. Brain and language 2016 Apr . Uddén Julia, Snijders Tineke M, Fisher Simon E, Hagoort Pet |
| The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2017 Mar . Zare Sahar, Mashayekhi Farhad, Bidabadi Elh |
| Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome. International ophthalmology 2017 Dec . Karaca Irmak, Yilmaz Suzan Guven, Palamar Melis, Onay Huseyin, Akgun Bilcag, Aytacoglu Burcu, Aykut Ayca, Ozkinay Feristah Fer |
| Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elements. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2017 10 20 (2): 126-136. Piluso Giulio, Monteleone Palmiero, Galderisi Silvana, Giugliano Teresa, Bertolino Alessandro, Rocca Paola, Rossi Alessandro, Mucci Armida, Aguglia Eugenio, Andriola Ileana, Bellomo Antonello, Comparelli Anna, Gambi Francesco, Fagiolini Andrea, Marchesi Carlo, Roncone Rita, Sacchetti Emilio, Santonastaso Paolo, Siracusano Alberto, Stratta Paolo, Tortorella Alfonso, Steardo Luca, Bucci Paola, Nigro Vincenzo, Maj Mario, |
| Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
| Sex differences in gene expression patterns associated with the APOE4 allele. F1000Research 2019 8 8 387. Hsu Michelle, Dedhia Mehek, Crusio Wim E, Delprato An |
| Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder. Behavioural neurology 2021 7 2021 4150926. Fang Fang, Ge Minxia, Liu Jun, Zhang Zengyu, Yu Hong, Zhu Shuilong, Xu Liwei, Shao Li |
| Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population. Genes 2021 Oct 12 (10): . Bocharova Anna, Vagaitseva Kseniya, Marusin Andrey, Zhukova Natalia, Zhukova Irina, Minaycheva Larisa, Makeeva Oksana, Stepanov Vad |
| Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder. Human genetics 2023 5 . Gianluca D'Onofrio, Andrea Accogli, Mariasavina Severino, Haluk Caliskan, Tomislav Kokotovi?, Antonela Blazekovic, Kristina Gotovac Jercic, Silvana Markovic, Tamara Zigman, Krnjak Goran, Nina Bariši?, Vlasta Duranovic, Ana Ban, Fran Borovecki, Danijela Petkovi? Ramadža, Ivo Bari?, Walid Fazeli, Peter Herkenrath, Carla Marini, Roberta Vittorini, Vykuntaraju Gowda, Arjan Bouman, Clarissa Rocca, Issam Azmi Alkhawaja, Bibi Nazia Murtaza, Malik Mujaddad Ur Rehman, Chadi Al Alam, Gisele Nader, Maria Margherita Mancardi, Thea Giacomini, Siddharth Srivastava, Javeria Raza Alvi, Hoda Tomoum, Sara Matricardi, Michele Iacomino, Antonella Riva, Marcello Scala, Francesca Madia, Angela Pistorio, Vincenzo Salpietro, Carlo Minetti, Jean-Baptiste Rivière, Myriam Srour, Stephanie Efthymiou, Reza Maroofian, Henry Houlden, Sonja Catherine Vernes, Federico Zara, Pasquale Striano, Vanja Na |
| Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population. Heliyon 2024 6 10 (11): e31624. Paolina Crocco, Francesco De Rango, Francesco Bruno, Antonio Malvaso, Raffaele Maletta, Amalia C Bruni, Giuseppe Passarino, Giuseppina Rose, Serena Da |
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