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| Discovery of eQTL Alleles Associated with Autism Spectrum Disorder: A Case-Control Study. Journal of autism and developmental disorders 2022 Jun . Hickman Allison R, Selee Bradley, Pauly Rini, Husain Benafsh, Hang Yuqing, Feltus Frank Al |
| Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci. Human molecular genetics 2021 Nov . Laaksonen Jaakko, Mishra Pashupati P, Seppälä Ilkka, Raitoharju Emma, Marttila Saara, Mononen Nina, Lyytikäinen Leo-Pekka, Kleber Marcus E, Delgado Graciela E, Lepistö Maija, Almusa Henrikki, Ellonen Pekka, Lorkowski Stefan, März Winfried, Hutri-Kähönen Nina, Raitakari Olli, Kähönen Mika, Salonen Jukka T, Lehtimäki Ter |
| Communication processes about predictive genetic testing within high-risk breast cancer families: a two-phase study design. Scientific reports 2021 Oct 11 (1): 20178. Blomen Chiara L, Pott Aliaksandra, Volk Alexander E, Budäus Lars, Witzel Isabe |
| Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation. The Journal of craniofacial surgery 2021 Jul . Kilcoyne Sarah, Luscombe Carrie, Scully Paula, Overton Sarah, Brockbank Sally, Swan Marc C, Johnson David, Wall Steven, Wilkie Andrew O |
Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.
Genes 2021 May 12 (5): . Al-Sarraj Yasser, Al-Dous Eman, Taha Rowaida Z, Ahram Dina, Alshaban Fouad, Tolfat Mohammed, El-Shanti Hatem, Albagha Omar M |
| The interaction of child abuse and rs1360780 of the FKBP5 gene is associated with amygdala resting-state functional connectivity in young adults. Human brain mapping 2021 Apr . Wesarg Christiane, Veer Ilya M, Oei Nicole Y L, Daedelow Laura S, Lett Tristram A, Banaschewski Tobias, Barker Gareth J, Bokde Arun L W, Quinlan Erin Burke, Desrivières Sylvane, Flor Herta, Grigis Antoine, Garavan Hugh, Brühl Rüdiger, Martinot Jean-Luc, Artiges Eric, Nees Frauke, Orfanos Dimitri Papadopoulos, Poustka Luise, Hohmann Sarah, Fröhner Juliane H, Smolka Michael N, Whelan Robert, Schumann Gunter, Heinz Andreas, Walter Henrik, |
| A pioneering study indicate role of GABRQ rs3810651 in ASD severity of Indo-Caucasoid female probands. Scientific reports 2021 Mar 11 (1): 7010. Saha Sharmistha, Chatterjee Mahasweta, Sinha Swagata, Mukhopadhyay Kanch |
| Assessment of children in the autistic spectrum disorder that carry the Thr92Ala-DIO2 polymorphism. Journal of endocrinological investigation 2021 Jan . E Marcondes A A, Gomez T G B, Ravache T T, Batistuzzo A, Lorena F B, de Paula C S, Lowenthal R, Bianco A C, Ribeiro M |
| Physical Fitness and Apolipoprotein E Genotype Influence Cortical Networking and Intelligence in Adolescents. The journal of prevention of Alzheimer's disease 2021 8 (1): 92-99. Park J, Kim Y, Woo |
| The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
Nature communications 2021 05 12 (1): 2909. Elvsåshagen Torbjørn, Shadrin Alexey, Frei Oleksandr, van der Meer Dennis, Bahrami Shahram, Kumar Vinod Jangir, Smeland Olav, Westlye Lars T, Andreassen Ole A, Kaufmann Tobi |
| A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
| Genetic Risk of Autism Spectrum Disorder in a Pakistani Population. Genes 2020 Oct 11 (10): . Khalid Madiha, Raza Hashim, M Driessen Terri, J Lee Paul, Tejwani Leon, Sami Abdul, Nawaz Muhammad, Mehmood Baig Shahid, Lim Janghoo, Kaukab Raja Ghaza |
| Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
Molecular biology reports 2020 Oct 47 (10): 7623-7632. Alsubaie Laila M, Alsuwat Hind Saleh, Almandil Noor B, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
| Short Communication: Genetic Variation in Human IL10 Proximal Promoter and Susceptibility to HIV-1 Infection in Mali, West Africa. AIDS research and human retroviruses 2020 Oct . Dabitao Djeneba, Dembele Mamadou, Urbanowski Michael, Kone Bourahima, Wague Mamadou, Coulibaly Nadie, Sarro Yeya Dit Sadio, Baya Bocar, Goita Drissa, Dao Sounkalo, Belson Michael, Klein Sabra, Achenbach Chad, Holl Jane, Diakite Mahamadou, Doumbia Seydou, Bream Jay H, Bishai William, Diallo Souleymane, Murphy Robe |
| Association of the MTHFR 677C>T and 1298A>C polymorphisms and male infertility risk: a meta-analysis. Reproductive biology and endocrinology : RB&E 2020 Sep 18 (1): 93. Aliakbari Fereshteh, Pouresmaeili Farkhondeh, Eshghifar Nahal, Zolghadr Zahra, Azizi Faez |
| Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Translational psychiatry 2020 Jul 10 (1): 215. Yousaf Afsheen, Waltes Regina, Haslinger Denise, Klauck Sabine M, Duketis Eftichia, Sachse Michael, Voran Anette, Biscaldi Monica, Schulte-Rüther Martin, Cichon Sven, Nöthen Markus, Ackermann Jörg, Koch Ina, Freitag Christine M, Chiocchetti Andreas |
| A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior.
Molecular psychiatry 2020 May . Meyers Jacquelyn L, Zhang Jian, Chorlian David B, Pandey Ashwini K, Kamarajan Chella, Wang Jen-Chyong, Wetherill Leah, Lai Dongbing, Chao Michael, Chan Grace, Kinreich Sivan, Kapoor Manav, Bertelsen Sarah, McClintick Jeanette, Bauer Lance, Hesselbrock Victor, Kuperman Samuel, Kramer John, Salvatore Jessica E, Dick Danielle M, Agrawal Arpana, Foroud Tatiana, Edenberg Howard J, Goate Alison, Porjesz Berni |
| Prenatally detected copy number variants in a national cohort: A postnatal follow-up study. Prenatal diagnosis 2020 May . Muys Joke, Jacquemyn Yves, Blaumeiser Bettina, Bourlard Laura, Brison Nathalie, Bulk Saskia, Chiarappa Patrizia, De Leener Anne, De Rademaeker Marjan, Désir Julie, Destrée Anne, Devriendt Koenraad, Dheedene Annelies, Duquenne Armelle, Fieuw Annelies, Fransen Erik, Gatot Jean-Stéphane, Jamar Mauricette, Janssens Sandra, Kerstjens Jorien, Keymolen Kathelijn, Lederer Damien, Menten Björn, Pichon Bruno, Rombout Sonia, Sznajer Yves, Van Den Bogaert Ann, Van Den Bogaert Kris, Vermeesch Joris, Janssens Katri |
| SNP rs12982687 affects binding capacity of lncRNA UCA1 with miR-873-5p: involvement in smoking-triggered colorectal cancer progression. Cell communication and signaling : CCS 2020 Mar 18 (1): 37. Fu Yang, Zhang Yizheng, Cui Jinyuan, Yang Ge, Peng Sanfei, Mi Wunan, Yin Xiangya, Yu Yang, Jiang Jianwu, Liu Qi, Qin Yiyu, Xu W |
| Effects of COMT rs4680 and BDNF rs6265 polymorphisms on brain degree centrality in Han Chinese adults who lost their only child. Translational psychiatry 2020 Jan 10 (1): 46. Qi Rongfeng, Luo Yifeng, Zhang Li, Weng Yifei, Surento Wesley, Li Lingjiang, Cao Zhihong, Lu Guang Mi |
| Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell 2020 Jan . Satterstrom F Kyle, Kosmicki Jack A, Wang Jiebiao, Breen Michael S, De Rubeis Silvia, An Joon-Yong, Peng Minshi, Collins Ryan, Grove Jakob, Klei Lambertus, Stevens Christine, Reichert Jennifer, Mulhern Maureen S, Artomov Mykyta, Gerges Sherif, Sheppard Brooke, Xu Xinyi, Bhaduri Aparna, Norman Utku, Brand Harrison, Schwartz Grace, Nguyen Rachel, Guerrero Elizabeth E, Dias Caroline, , , Betancur Catalina, Cook Edwin H, Gallagher Louise, Gill Michael, Sutcliffe James S, Thurm Audrey, Zwick Michael E, Børglum Anders D, State Matthew W, Cicek A Ercument, Talkowski Michael E, Cutler David J, Devlin Bernie, Sanders Stephan J, Roeder Kathryn, Daly Mark J, Buxbaum Joseph |
| Motor learning and COMT Val158met polymorphism: Analyses of oculomotor behavior and corticocortical communication. Neurobiology of learning and memory 2020 Jan 107157. Gardênia de Holanda Marinho Nogueira Nathálya, Marques de Miranda Débora, Rodrigues Albuquerque Maicon, de Paula Ferreira Bárbara, Túlio Silva Batista Marco, Otoni Parma Juliana, Apolinário-Souza Tércio, Eduardo Antunes Bicalho Lucas, Ugrinowitsch Herbert, Menezes Lage Guilher |
| Proprotein convertase 7 (PCSK7) reduces apoA-V levels. The FEBS journal 2020 Jan . Ashraf Yahya, Duval Stéphanie, Sachan Vatsal, Essalmani Rachid, Susan-Resiga Delia, Roubtsova Anna, Hamelin Josée, Gerhardy Stefan, Kirchhofer Daniel, Tagliabracci Vincent S, Prat Annik, Kiss Robert Scott, Seidah Nabil |
| Non-classical human leukocyte antigen class I in Tunisian children with autism. Central-European journal of immunology 2020 45 (2): 176-183. Kharrat Najla, Abdelhedi Rania, Gtif Imen, Ayadi Imen, Rizzo Roberta, Bortolotti Daria, Abdelmoula Nouha Bouayed, Ghribi Farhat, Rebai Ahmed, Zidi In |
| Sex-dependent effects of Cacna1c haploinsufficiency on behavioral inhibition evoked by conspecific alarm signals in rats. Progress in neuro-psychopharmacology & biological psychiatry 2019 Dec 109849. Wöhr Markus, Willadsen Maria, Kisko Theresa M, Schwarting Rainer K W, Fendt Mark |
| Short Communication: The Association of WNT16 Polymorphisms with the CD4 T Cell Count in the HIV-Infected Population. AIDS research and human retroviruses 2019 Oct . Xie Li, Huang Yiyong, Zhong Jianing, Wei Huiping, Chen Siyuan, Jiang Kongmei, Li Shan, Qin X |
| Variation near MTNR1A associates with early development and interacts with seasons. Journal of sleep research 2019 Oct e12925. Sulkava Sonja, Taka Antti-Mathias, Kantojärvi Katri, Pölkki Pirjo, Morales-Muñoz Isabel, Milani Lili, Porkka-Heiskanen Tarja, Saarenpää-Heikkilä Outi, Kylliäinen Anneli, Juulia Paavonen E, Paunio Tii |
| A single nucleotide polymorphism (-250 A/C) of the GFAP gene is associated with brain structures and cerebral blood flow. Psychiatry and clinical neurosciences 2019 Sep . Takahashi Yuta, Takeuchi Hikaru, Sakai Mai, Yu Zhiqian, Kikuchi Yoshie, Ito Fumiaki, Matsuoka Hiroo, Tanabe Osamu, Yasuda Jun, Taki Yasuyuki, Kawashima Ryuta, Tomita Hiroa |
| rs1360780 of the FKBP5 gene modulates the association between maternal acceptance and regional gray matter volume in the thalamus in children and adolescents. PloS one 2019 14 (8): e0221768. Matsudaira Izumi, Oba Kentaro, Takeuchi Hikaru, Sekiguchi Atsushi, Tomita Hiroaki, Taki Yasuyuki, Kawashima Ryu |
| Social and non-social autism symptoms and trait domains are genetically dissociable.
Communications biology 2019 2 328. Warrier Varun, Toro Roberto, Won Hyejung, Leblond Claire S, Cliquet Freddy, Delorme Richard, De Witte Ward, Bralten Janita, Chakrabarti Bhismadev, Børglum Anders D, Grove Jakob, Poelmans Geert, Hinds David A, Bourgeron Thomas, Baron-Cohen Sim |
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- Page last updated:Aug 16, 2022
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