Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: Schizophrenia and MAF[original query] |
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Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Apr 153B (3): 766-74. Dwyer S, Carroll L, Mantripragada K K, Owen M J, O'Donovan M C, Williams N |
Lack of association between PRNP M129V polymorphism and multiple sclerosis, mild cognitive impairment, alcoholism and schizophrenia in a Korean population. Disease markers 2010 28 (5): 315-21. Choi Ihn-Geun, Woo Sung-Il, Kim Ho Jin, Kim Dai-Jin, Park Byung Lae, Cheong Hyun Sub, Pasaje Charisse Flerida A, Park Tae Joon, Bae Joon Seol, Chai Young Gyu, Shin Hyoung D |
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. PloS one 2011 6 (8): e23450. Moens Lotte N, De Rijk Peter, Reumers Joke, Van den Bossche Maarten J A, Glassee Wim, De Zutter Sonia, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, Medina Castello Ignacio, Norrback Karl-Fredrik, Goossens Dirk, Van Steen Kristel, Adolfsson Rolf, Del-Favero Jurg |
Association of PDE4B polymorphisms and schizophrenia in Northwestern Han Chinese. Human genetics 2012 Jul 131 (7): 1047-56. Guan Fanglin, Zhang Chen, Wei Shuguang, Zhang Hongbo, Gong Xiaomin, Feng Jiali, Gao Chengge, Su Rong, Yang Huanming, Li Shengb |
The C allele of synonymous SNP (rs1142636, Asn170Asn) in SYN1 is a risk factor for the susceptibility of Korean female schizophrenia. Synapse (New York, N.Y.) 2012 Nov 66 (11): 979-83. Yu Gyeong Im, Kim Su Kang, Park Hae Jeong, Kim Jong Woo, Chung Joo-Ho, Shin Dong Ho |
ASTN1 and alcohol dependence: family-based association analysis in multiplex alcohol dependence families. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jun 159B (4): 445-55. Hill Shirley Y, Weeks Daniel E, Jones Bobby L, Zezza Nicholas, Stiffler Sco |
A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Translational psychiatry 2013 3 e301. Martin P-M, Yang X, Robin N, Lam E, Rabinowitz J S, Erdman C A, Quinn J, Weiss L A, Hamilton S P, Kwok P-Y, Moon R T, Cheyette B N |
Association between common alcohol dehydrogenase gene (ADH) variants and schizophrenia and autism. Human genetics 2013 Jul 132 (7): 735-43. Zuo Lingjun, Wang Kesheng, Zhang Xiang-Yang, Pan Xinghua, Wang Guilin, Tan Yunlong, Zhong Chunlong, Krystal John H, State Matthew, Zhang Heping, Luo Xinggua |
Resequencing and association study of the NFKB activating protein-like gene (NKAPL) in schizophrenia. Schizophrenia research 2014 Aug 157 (1-3): 169-74. Chen Shih-Fen, Chao Yu-Lin, Shen Yu-Chih, Chen Chia-Hsiang, Weng Ching-Fe |
A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder. American journal of human genetics 2014 Dec 95 (6): 744-53. Duan Jubao, Shi Jianxin, Fiorentino Alessia, Leites Catherine, Chen Xiangning, Moy Winton, Chen Jingchun, Alexandrov Boian S, Usheva Anny, He Deli, Freda Jessica, O'Brien Niamh L, , , McQuillin Andrew, Sanders Alan R, Gershon Elliot S, DeLisi Lynn E, Bishop Alan R, Gurling Hugh M D, Pato Michele T, Levinson Douglas F, Kendler Kenneth S, Pato Carlos N, Gejman Pablo |
Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk. Schizophrenia bulletin 2015 Sep . Kos Mark Z, Carless Melanie A, Peralta Juan, Blackburn August, Almeida Marcio, Roalf David, Pogue-Geile Michael F, Prasad Konasale, Gur Ruben C, Nimgaonkar Vishwajit, Curran Joanne E, Duggirala Ravi, Glahn David C, Blangero John, Gur Raquel E, Almasy Lau |
Selection in the dopamine receptor 2 gene: a candidate SNP study. PeerJ 2015 3 e1149. Göllner Tobias, Fieder Mart |
Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational psychiatry 2015 5 e607. Rees E, Kirov G, Walters J T, Richards A L, Howrigan D, Kavanagh D H, Pocklington A J, Fromer M, Ruderfer D M, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, Johnson J S, Roussos P, Barker D D, Banks E, Milanova V, Rose S A, Chambert K, Mahajan M, Scolnick E M, Moran J L, Tsuang M T, Glatt S J, Chen W J, Hwu H-G, , Neale B M, Palotie A, Sklar P, Purcell S M, McCarroll S A, Holmans P, Owen M J, O'Donovan M |
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jul . Leonenko Ganna, Richards Alexander L, Walters James T, Pocklington Andrew, Chambert Kimberly, Al Eissa Mariam M, Sharp Sally I, O'Brien Niamh L, Curtis David, Bass Nicholas J, McQuillin Andrew, Hultman Christina, Moran Jennifer L, McCarroll Steven A, Sklar Pamela, Neale Benjamin M, Holmans Peter A, Owen Michael J, Sullivan Patrick F, O'Donovan Michael |
Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia. Schizophrenia research 2017 Feb . John Jibin, Kukshal Prachi, Bhatia Triptish, Chowdari K V, Nimgaonkar V L, Deshpande S N, Thelma B |
Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis. Schizophrenia bulletin 2018 2 45 (1): 256-263. John Jibin, Sharma Aditya, Kukshal Prachi, Bhatia Triptish, Nimgaonkar Vishwajit L, Deshpande Smita N, Thelma B |
Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study. Schizophrenia research 2018 12 206 75-81. John Jibin, Kukshal Prachi, Sharma Aditya, Bhatia Triptish, Nimgaonkar V L, Deshpande S N, Thelma B |
Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study. Molecular psychiatry 2020 Jul . Thygesen Johan H, Presman Amelia, Harju-Seppänen Jasmine, Irizar Haritz, Jones Rebecca, Kuchenbaecker Karoline, Lin Kuang, Alizadeh Behrooz Z, Austin-Zimmerman Isabelle, Bartels-Velthuis Agna, Bhat Anjali, Bruggeman Richard, Cahn Wiepke, Calafato Stella, Crespo-Facorro Benedicto, de Haan Liewe, de Zwarte Sonja M C, Di Forti Marta, Díez-Revuelta Álvaro, Hall Jeremy, Hall Mei-Hua, Iyegbe Conrad, Jablensky Assen, Kahn Rene, Kalaydjieva Luba, Kravariti Eugenia, Lawrie Stephen, Luykx Jurjen J, Mata Igancio, McDonald Colm, McIntosh Andrew M, McQuillin Andrew, Muir Rebecca, Ophoff Roel, Picchioni Marco, Prata Diana P, Ranlund Siri, Rujescu Dan, Rutten Bart P F, Schulze Katja, Shaikh Madiha, Schirmbeck Frederike, Simons Claudia J P, Toulopoulou Timothea, van Amelsvoort Therese, van Haren Neeltje, van Os Jim, van Winkel Ruud, Vassos Evangelos, Walshe Muriel, Weisbrod Matthias, Zartaloudi Eirini, Bell Vaughan, Powell John, Lewis Cathryn M, Murray Robin M, Bramon Elvi |
Reproducible Genetic Risk Loci for Anxiety: Results From ~200,000 Participants in the Million Veteran Program.
The American journal of psychiatry 2020 03 177 (3): 223-232. Levey Daniel F, Gelernter Joel, Polimanti Renato, Zhou Hang, Cheng Zhongshan, Aslan Mihaela, Quaden Rachel, Concato John, Radhakrishnan Krishnan, Bryois Julien, Sullivan Patrick F, , Stein Murray |
Chromosomal region 1q24.1 is associated with increased risk of schizophrenia in Pakistani population. Gene 2020 1 734 144390. Fatima Warda, Riaz Sabeen, Aiman Shahzad Muhammad, Naz Zara, Mahmood Saqib, Hasnain Shahi |
Association between C-Maf-inducing protein gene rs2287112 polymorphism and schizophrenia. PeerJ 2021 9 9 e11907. Fu Yingli, Ren Xiaojun, Bai Wei, Yu Qiong, Sun Yaoyao, Yu Yaqin, Zhou |
Association of Variants in COMT, RASSF1 and GPM6A with the Risk of Paranoid Schizophrenia Patients in Prof HB Saanin Psychiatric Hospital, West Sumatra, Indonesia. The Malaysian journal of medical sciences : MJMS 2022 Apr 29 (2): 31-42. Yunaini Luluk, Khairat Edwi |
Mitochondrial genetic variants associated with bipolar disorder and Schizophrenia in a Japanese population. International journal of bipolar disorders 2023 7 11 (1): 26. Ryobu Tachi, Kazutaka Ohi, Daisuke Nishizawa, Midori Soda, Daisuke Fujikane, Junko Hasegawa, Ayumi Kuramitsu, Kentaro Takai, Yukimasa Muto, Shunsuke Sugiyama, Kiyoyuki Kitaichi, Ryota Hashimoto, Kazutaka Ikeda, Toshiki Shioi |
Common and rare variant associations with latent traits underlying depression, bipolar disorder, and schizophrenia. Translational psychiatry 2023 2 13 (1): 46. Dattani Saloni, Sham Pak C, Jermy Bradley S, Coleman Jonathan R I, Howard David M, Lewis Cathryn |
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- Page last updated:Apr 16, 2024
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