| Year |
Citation |
Score |
| 2023 |
Ahangari M, Gentry AE, Hassan MF, Nguyen TH, Kendler KS, Bacanu SA, Peterson RE, Riley BP, Webb BT. Improving the discovery of rare variants associated with alcohol problems by leveraging machine learning phenotype prediction and functional information. Biorxiv : the Preprint Server For Biology. PMID 37745400 DOI: 10.1101/2023.09.11.557163 |
0.308 |
|
| 2023 |
Gedik H, Peterson RE, Riley BP, Vladimirov VI, Bacanu SA. Integrative Post-Genome-Wide Association Study Analyses Relevant to Psychiatric Disorders: Imputing Transcriptome and Proteome Signals. Complex Psychiatry. 9: 130-144. PMID 37588130 DOI: 10.1159/000530223 |
0.331 |
|
| 2023 |
Gedik H, Nguyen TH, Peterson RE, Chatzinakos C, Vladimirov VI, Riley BP, Bacanu SA. Identifying potential risk genes and pathways for neuropsychiatric and substance use disorders using intermediate molecular mediator information. Frontiers in Genetics. 14: 1191264. PMID 37415601 DOI: 10.3389/fgene.2023.1191264 |
0.335 |
|
| 2022 |
Ahangari M, Kirkpatrick R, Nguyen TH, Gillespie N, Kendler KS, Bacanu SA, Webb BT, Verrelli BC, Riley BP. Examining the source of increased bipolar disorder and major depressive disorder common risk variation burden in multiplex schizophrenia families. Schizophrenia (Heidelberg, Germany). 8: 106. PMID 36434002 DOI: 10.1038/s41537-022-00317-w |
0.311 |
|
| 2022 |
Ahangari M, Everest E, Nguyen TH, Verrelli BC, Webb BT, Bacanu SA, Tahir Turanli E, Riley BP. Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects. Brain, Behavior, and Immunity. 104: 183-190. PMID 35714915 DOI: 10.1016/j.bbi.2022.06.007 |
0.316 |
|
| 2022 |
Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Riley BP, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5 |
0.365 |
|
| 2021 |
Chatzinakos C, Lee D, Cai N, Vladimirov VI, Webb BT, Riley BP, Flint J, Kendler KS, Ressler KJ, Daskalakis NP, Bacanu SA. Increasing the resolution and precision of psychiatric genome-wide association studies by re-imputing summary statistics using a large, diverse reference panel. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 33576176 DOI: 10.1002/ajmg.b.32834 |
0.313 |
|
| 2020 |
Johnson EC, Demontis D, Thorgeirsson TE, Walters RK, Polimanti R, Hatoum AS, Sanchez-Roige S, Paul SE, Wendt FR, Clarke TK, Lai D, Reginsson GW, Zhou H, He J, Baranger DAA, ... ... Riley BP, et al. A large-scale genome-wide association study meta-analysis of cannabis use disorder. The Lancet. Psychiatry. PMID 33096046 DOI: 10.1016/S2215-0366(20)30339-4 |
0.733 |
|
| 2020 |
Chatzinakos C, Georgiadis F, Lee D, Cai N, Vladimirov VI, Docherty A, Webb BT, Riley BP, Flint J, Kendler KS, Daskalakis NP, Bacanu SA. TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32954640 DOI: 10.1002/Ajmg.B.32823 |
0.444 |
|
| 2020 |
Nguyen TH, Dobbyn A, Brown RC, Riley BP, Buxbaum JD, Pinto D, Purcell SM, Sullivan PF, He X, Stahl EA. mTADA is a framework for identifying risk genes from de novo mutations in multiple traits. Nature Communications. 11: 2929. PMID 32522981 DOI: 10.1038/S41467-020-16487-Z |
0.433 |
|
| 2020 |
Polimanti R, Walters RK, Johnson EC, McClintick JN, Adkins AE, Adkins DE, Bacanu SA, Bierut LJ, Bigdeli TB, Brown S, Bucholz KK, Copeland WE, Costello EJ, Degenhardt L, Farrer LA, ... ... Riley BP, et al. Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Molecular Psychiatry. PMID 32099098 DOI: 10.1038/S41380-020-0677-9 |
0.723 |
|
| 2020 |
Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Hübel C, Gordon S, Medland SE, Watson HJ, Gaspar HA, Bryois J, Hinney A, ... ... Riley BP, et al. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology. e12880. PMID 32064741 DOI: 10.1111/Adb.12880 |
0.736 |
|
| 2019 |
Chen J, Loukola A, Gillespie NA, Peterson R, Jia P, Riley B, Maes H, Dick DM, Kendler KS, Damaj MI, Miles MF, Zhao Z, Li MD, Vink JM, Minica CC, et al. Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. PMID 31294817 DOI: 10.1093/Ntr/Ntz099 |
0.304 |
|
| 2019 |
Mignogna KM, Bacanu SA, Riley BP, Wolen AR, Miles MF. Cross-species alcohol dependence-associated gene networks: Co-analysis of mouse brain gene expression and human genome-wide association data. Plos One. 14: e0202063. PMID 31017905 DOI: 10.1371/Journal.Pone.0202063 |
0.433 |
|
| 2019 |
Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J, Donohoe G, Gill M, Corvin A, et al. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30801977 DOI: 10.1002/Ajmg.B.32716 |
0.437 |
|
| 2019 |
Ahangari M, Gentry A, Kealhofer M, Sun C, Wormley B, Bacanu S, Webb BT, Kendler K, Riley B. S92Exome Variation In Ethanol Metabolizing Enzyme Genes In Irish Severe Alcohol Dependence (Ad) Cases European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.093 |
0.337 |
|
| 2019 |
Nguyen T, Charney A, He X, Kendler K, Sullivan P, Bacanu S, Riley B, Stahl E. 13 INTEGRATED ANALYSIS OF RARE VARIANTS AND SINGLE-CELL EXPRESSION DATA PROVIDES INSIGHTS INTO SCHIZOPHRENIA RISK European Neuropsychopharmacology. 29: S65-S66. DOI: 10.1016/J.Euroneuro.2019.07.154 |
0.367 |
|
| 2019 |
Riley B, Corvin A, Stefansson H, Kenny E, Morris D, Donohoe G, Waddington J, Webb B, Bacanu S, Gill M, Kendler K, Stefansson K. F122Whole Genome Sequencing Of Schizophrenia In Ireland European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.202 |
0.343 |
|
| 2019 |
Rietschel M, Riley B. Approaches To Genomic Studies Of Alcohol Dependence And Co-Morbid Disorders European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.07.029 |
0.395 |
|
| 2019 |
Alexander J, Bacanu S, Kendler K, Webb B, Riley B. Exome Sequencing In Severe Alcohol Use Disorder Cases European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.418 |
0.467 |
|
| 2019 |
Mignogna K, Riley B, Bacanu S, Wolen A, Miles M. Cross-Species Analysis Of Alcohol-Regulated And Dependence-Associated Gene Networks In The Ventral Tegmental Area European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.181 |
0.441 |
|
| 2018 |
Walters RK, Polimanti R, Johnson EC, McClintick JN, Adams MJ, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Chou YL, ... ... Riley BP, et al. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience. 21: 1656-1669. PMID 30482948 DOI: 10.1038/S41593-018-0275-1 |
0.766 |
|
| 2018 |
Xia H, Jahr FM, Kim NK, Xie L, Shabalin AA, Bryois J, Sweet DH, Kronfol MM, Palasuberniam P, McRae M, Riley BP, Sullivan PF, van den Oord EJ, McClay JL. Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk. Human Molecular Genetics. PMID 29905862 DOI: 10.1093/Hmg/Ddy222 |
0.373 |
|
| 2018 |
Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Riley BP, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3 |
0.403 |
|
| 2018 |
Savage JE, Salvatore JE, Aliev F, Edwards AC, Hickman M, Kendler KS, Macleod J, Latvala A, Loukola A, Kaprio J, Rose RJ, Chan G, Hesselbrock V, Webb BT, Adkins A, ... ... Riley BP, et al. Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population-Based and Clinically Ascertained Samples. Alcoholism, Clinical and Experimental Research. PMID 29405378 DOI: 10.1111/Acer.13589 |
0.743 |
|
| 2017 |
Farris SP, Riley BP, Williams RW, Mulligan MK, Miles MJ, Lopez MF, Hitzemann R, Iancu OD, Colville A, Walter NAR, Darakjian P, Oberbeck DL, Daunais JB, Zheng CL, Searles RP, et al. Cross-species molecular dissection across alcohol behavioral domains. Alcohol (Fayetteville, N.Y.). PMID 30213503 DOI: 10.1016/J.Alcohol.2017.11.036 |
0.428 |
|
| 2017 |
Docherty AR, Moscati A, Dick D, Savage JE, Salvatore JE, Cooke M, Aliev F, Moore AA, Edwards AC, Riley BP, Adkins DE, Peterson R, Webb BT, Bacanu SA, Kendler KS. Polygenic prediction of the phenome, across ancestry, in emerging adulthood. Psychological Medicine. 1-10. PMID 29173193 DOI: 10.1017/S0033291717003312 |
0.396 |
|
| 2017 |
Webb BT, Edwards AC, Wolen AR, Salvatore JE, Aliev F, Riley BP, Sun C, Williamson VS, Kitchens JN, Pedersen K, Adkins A, Cooke ME, Savage JE, Neale Z, Cho SB, et al. Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students. Frontiers in Genetics. 8: 30. PMID 28360924 DOI: 10.3389/Fgene.2017.00030 |
0.749 |
|
| 2017 |
Bigdeli TB, Ripke S, Peterson RE, Trzaskowski M, Bacanu SA, Abdellaoui A, Andlauer TF, Beekman AT, Berger K, Blackwood DH, Boomsma DI, Breen G, Buttenschøn HN, Byrne EM, Cichon S, ... ... Riley BP, et al. Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry. 7: e1074. PMID 28350396 DOI: 10.1038/Tp.2016.292 |
0.48 |
|
| 2017 |
Adkins AE, Hack LM, Bigdeli TB, Williamson VS, McMichael GO, Mamdani M, Edwards A, Aliev F, Chan RF, Bhandari P, Raabe RC, Alaimo JT, Blackwell GG, Moscati AA, Poland RS, ... ... Riley BP, et al. Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-response Behaviors in Model Organisms. Alcoholism, Clinical and Experimental Research. PMID 28226201 DOI: 10.1111/Acer.13362 |
0.735 |
|
| 2017 |
Cai N, Bigdeli TB, Kretzschmar WW, Li Y, Liang J, Hu J, Peterson RE, Bacanu S, Webb BT, Riley B, Li Q, Marchini J, Mott R, Kendler KS, Flint J. 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project. Scientific Data. 4: 170011. PMID 28195579 DOI: 10.1038/Sdata.2017.11 |
0.415 |
|
| 2017 |
Docherty A, Adkins D, Kendler K, Riley B, Corvin A, Fanous A, Bacanu S. 127. Pathway-Based Molecular Subtyping of Schizophrenia Accounting for Population Stratification and Sex Schizophrenia Bulletin. 43: S70-S70. DOI: 10.1093/Schbul/Sbx021.185 |
0.326 |
|
| 2017 |
Moscati A, Docherty A, Savage J, Salvatore J, Cooke M, Aliev F, Moore A, Peterson R, Edwards A, Riley B, Adkins D, Webb B, Dick D, Bacanu S, Kendler K. Genome-Wide Polygenic Atlas of the Phenome in Emerging Adulthood: Prediction of Behavioral and Health Outcomes European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.610 |
0.388 |
|
| 2017 |
Aliev F, Bin Cho S, Grotewiel M, Bettinger J, Mathies L, Riley B, Alexander J, Davies A, Webb T, Kendler K, Miles M, Dick D. Studies Of Alcohol Related Phenotypes Across Human, Mouse And Invertebrate Models European Neuropsychopharmacology. 27: S467. DOI: 10.1016/J.Euroneuro.2016.09.544 |
0.45 |
|
| 2017 |
Docherty A, Moscati A, Savage J, Salvatore J, Cooke M, Aliev F, Moore A, Peterson R, Edwards A, Riley B, Adkins D, Webb B, Dick D, Bacanu S, Kendler K. Genome-Wide Polygenic Atlas of The Phenome In Emerging Adulthood: Genetic Overlap of Risk Across Five Ancestries European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.440 |
0.467 |
|
| 2017 |
Bettinger J, Bowers M, Grotewiel M, Kendler K, Miles M, Vladimirov V, Webb B, Riley B. Cross-species convergence in the genetics of ethanol response and alcohol dependence Alcohol. 60: 213-214. DOI: 10.1016/J.Alcohol.2017.02.228 |
0.339 |
|
| 2016 |
Peterson RE, Cai N, Bigdeli TB, Li Y, Reimers M, Nikulova A, Webb BT, Bacanu SA, Riley BP, Flint J, Kendler KS. The Genetic Architecture of Major Depressive Disorder in Han Chinese Women. Jama Psychiatry. PMID 28002544 DOI: 10.1001/Jamapsychiatry.2016.3578 |
0.409 |
|
| 2016 |
Bigdeli TB, Lee D, Webb BT, Riley BP, Vladimirov VI, Fanous AH, Kendler KS, Bacanu SA. A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans. Bioinformatics (Oxford, England). PMID 27187203 DOI: 10.1093/Bioinformatics/Btw303 |
0.305 |
|
| 2015 |
Latendresse SJ, Henry DB, Aggen SH, Byck GR, Ashbeck AW, Bolland JM, Sun C, Riley BP, Mustanski B, Dick DM. Dimensionality and Genetic Correlates of Problem Behavior in Low-Income African American Adolescents. Journal of Clinical Child and Adolescent Psychology : the Official Journal For the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53. 1-16. PMID 26514393 DOI: 10.1080/15374416.2015.1070353 |
0.359 |
|
| 2015 |
Lee D, Williamson VS, Bigdeli TB, Riley BP, Webb BT, Fanous AH, Kendler KS, Vladimirov VI, Bacanu SA. JEPEGMIX: gene-level joint analysis of functional SNPs in cosmopolitan cohorts. Bioinformatics (Oxford, England). PMID 26428293 DOI: 10.1093/Bioinformatics/Btv567 |
0.384 |
|
| 2015 |
Mamdani M, Williamson V, McMichael GO, Blevins T, Aliev F, Adkins A, Hack L, Bigdeli T, D van der Vaart A, Web BT, Bacanu SA, Kalsi G, Kendler KS, Miles MF, ... ... Riley BP, et al. Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence. Plos One. 10: e0137671. PMID 26381263 DOI: 10.1371/Journal.Pone.0137671 |
0.706 |
|
| 2015 |
Edwards AC, Bigdeli TB, Docherty AR, Bacanu S, Lee D, de Candia TR, Moscati A, Thiselton DL, Maher BS, Wormley BK, Walsh D, O'Neill FA, Kendler KS, Riley BP, Fanous AH. Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes. Schizophrenia Bulletin. PMID 26316594 DOI: 10.1093/Schbul/Sbv119 |
0.462 |
|
| 2015 |
Albert D, Belsky DW, Crowley DM, Latendresse SJ, Aliev F, Riley B, Sun C, Dick DM, Dodge KA. Can genetics predict response to complex behavioral interventions? evidence from a genetic analysis of the Fast Track randomized control trial. Journal of Policy Analysis and Management : [the Journal of the Association For Public Policy Analysis and Management]. 34: 497-518. PMID 26106668 DOI: 10.1002/Pam.21811 |
0.339 |
|
| 2015 |
Lee D, Bigdeli TB, Williamson VS, Vladimirov VI, Riley BP, Fanous AH, Bacanu SA. DISTMIX: direct imputation of summary statistics for unmeasured SNPs from mixed ethnicity cohorts. Bioinformatics (Oxford, England). PMID 26059716 DOI: 10.1093/Bioinformatics/Btv348 |
0.369 |
|
| 2015 |
Docherty AR, Bigdeli TB, Edwards AC, Bacanu S, Lee D, Neale MC, Wormley BK, Walsh D, O'Neill FA, Riley BP, Kendler KS, Fanous AH. Genome-wide gene pathway analysis of psychotic illness symptom dimensions based on a new schizophrenia-specific model of the OPCRIT. Schizophrenia Research. 164: 181-6. PMID 25778617 DOI: 10.1016/J.Schres.2015.02.013 |
0.416 |
|
| 2015 |
Mathies LD, Blackwell GG, Austin MK, Edwards AC, Riley BP, Davies AG, Bettinger JC. SWI/SNF chromatin remodeling regulates alcohol response behaviors in Caenorhabditis elegans and is associated with alcohol dependence in humans. Proceedings of the National Academy of Sciences of the United States of America. 112: 3032-7. PMID 25713357 DOI: 10.1073/Pnas.1413451112 |
0.403 |
|
| 2015 |
Lee D, Williamson VS, Bigdeli TB, Riley BP, Fanous AH, Vladimirov VI, Bacanu SA. JEPEG: a summary statistics based tool for gene-level joint testing of functional variants. Bioinformatics (Oxford, England). 31: 1176-82. PMID 25505091 DOI: 10.1093/Bioinformatics/Btu816 |
0.41 |
|
| 2015 |
Cai N, Bigdeli TB, Kretzschmar W, Lei Y, Liang J, Song L, Hu J, Li Q, Jin W, Hu Z, Wang G, Wang L, Qian P, Liu Y, Jiang T, ... ... Riley B, et al. Sparse whole-genome sequencing identifies two loci for major depressive disorder Nature. 523: 588-591. DOI: 10.1038/Nature14659 |
0.393 |
|
| 2014 |
Dick DM, Nasim A, Edwards AC, Salvatore JE, Cho SB, Adkins A, Meyers J, Yan J, Cooke M, Clifford J, Goyal N, Halberstadt L, Ailstock K, Neale Z, Opalesky J, ... ... Riley B, et al. Spit for Science: launching a longitudinal study of genetic and environmental influences on substance use and emotional health at a large US university. Frontiers in Genetics. 5: 47. PMID 24639683 DOI: 10.3389/Fgene.2014.00047 |
0.714 |
|
| 2014 |
Heron EA, Cormican P, Donohoe G, O'Neill FA, Kendler KS, Riley BP, Gill M, Corvin AP, Morris DW. No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset. Schizophrenia Research. 154: 79-82. PMID 24560374 DOI: 10.1016/J.Schres.2014.01.038 |
0.446 |
|
| 2014 |
Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, ... ... Riley BP, et al. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics. 23: 3316-26. PMID 24474471 DOI: 10.1093/Hmg/Ddu025 |
0.446 |
|
| 2014 |
Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, ... ... Riley B, et al. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry. 19: 37-40. PMID 24217254 DOI: 10.1038/Mp.2013.156 |
0.397 |
|
| 2014 |
Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, ... ... Riley B, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics. 23: 1669-76. PMID 24163246 DOI: 10.1093/Hmg/Ddt540 |
0.442 |
|
| 2014 |
Schultz CC, Nenadic I, Riley B, Vladimirov VI, Wagner G, Koch K, Schachtzabel C, Mühleisen TW, Basmanav B, Nöthen MM, Deufel T, Kiehntopf M, Rietschel M, Reichenbach JR, Cichon S, et al. ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies. Schizophrenia Bulletin. 40: 532-41. PMID 24078172 DOI: 10.1093/Schbul/Sbt123 |
0.358 |
|
| 2014 |
Bigdeli TB, Bacanu SA, Webb BT, Walsh D, O'Neill FA, Fanous AH, Riley BP, Kendler KS. Molecular validation of the schizophrenia spectrum. Schizophrenia Bulletin. 40: 60-5. PMID 23970557 DOI: 10.1093/Schbul/Sbt122 |
0.426 |
|
| 2014 |
Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, ... ... Riley B, et al. Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 19: 108-14. PMID 23164818 DOI: 10.1038/Mp.2012.157 |
0.481 |
|
| 2014 |
Corvin A, Morris D, Pearson R, Cormican P, Kenny E, O'Neill F, Kendler K, Gill M, Riley B, Spencer C. 4:45 Pm Common And Rare Risk Variants Implicate Pak Signaling In The Molecular Etiology Of Schizophrenia Schizophrenia Research. 153. DOI: 10.1016/S0920-9964(14)70194-X |
0.366 |
|
| 2013 |
Lee D, Bigdeli TB, Riley BP, Fanous AH, Bacanu SA. DIST: direct imputation of summary statistics for unmeasured SNPs. Bioinformatics (Oxford, England). 29: 2925-7. PMID 23990413 DOI: 10.1093/Bioinformatics/Btt500 |
0.349 |
|
| 2013 |
Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, ... ... Riley BP, ... ... Riley BP, et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics. 45: 1150-9. PMID 23974872 DOI: 10.1038/Ng.2742 |
0.48 |
|
| 2013 |
Zhao Z, Webb BT, Jia P, Bigdeli TB, Maher BS, van den Oord E, Bergen SE, Amdur RL, O'Neill FA, Walsh D, Thiselton DL, Chen X, Pato CN, Riley BP, et al. Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. Plos One. 8: e67776. PMID 23922650 DOI: 10.1371/Journal.Pone.0067776 |
0.407 |
|
| 2013 |
Aberg KA, Liu Y, Bukszár J, McClay JL, Khachane AN, Andreassen OA, Blackwood D, Corvin A, Djurovic S, Gurling H, Ophoff R, Pato CN, Pato MT, Riley B, Webb T, et al. A comprehensive family-based replication study of schizophrenia genes. Jama Psychiatry. 70: 573-81. PMID 23894747 DOI: 10.1001/Jamapsychiatry.2013.288 |
0.425 |
|
| 2013 |
Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, ... ... Riley B, et al. Implication of a rare deletion at distal 16p11.2 in schizophrenia. Jama Psychiatry. 70: 253-60. PMID 23325106 DOI: 10.1001/2013.Jamapsychiatry.71 |
0.451 |
|
| 2013 |
Bigdeli TB, Fanous AH, Riley BP, Reimers M, Chen X, Kendler KS, Bacanu SA. On schizophrenia as a "disease of humanity". Schizophrenia Research. 143: 223-4. PMID 23182440 DOI: 10.1016/J.Schres.2012.10.036 |
0.383 |
|
| 2013 |
Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill FA, O'Neill T, Kendler KS, Sklar P, et al. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Molecular Psychiatry. 18: 708-12. PMID 22614287 DOI: 10.1038/Mp.2012.67 |
0.449 |
|
| 2012 |
Zhao Z, Guo AY, van den Oord EJ, Aliev F, Jia P, Edenberg HJ, Riley BP, Dick DM, Bettinger JC, Davies AG, Grotewiel MS, Schuckit MA, Agrawal A, Kramer J, Nurnberger JI, et al. Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study. Bmc Genomics. 13: S16. PMID 23282140 DOI: 10.1186/1471-2164-13-S8-S16 |
0.448 |
|
| 2012 |
Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, et al. Genome-wide association study of multiplex schizophrenia pedigrees. The American Journal of Psychiatry. 169: 963-73. PMID 22885689 DOI: 10.1176/Appi.Ajp.2012.11091423 |
0.471 |
|
| 2012 |
Webb BT, Guo AY, Maher BS, Zhao Z, van den Oord EJ, Kendler KS, Riley BP, Gillespie NA, Prescott CA, Middeldorp CM, Willemsen G, de Geus EJ, Hottenga JJ, Boomsma DI, Slagboom EP, et al. Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics : Ejhg. 20: 1078-84. PMID 22473089 DOI: 10.1038/Ejhg.2012.47 |
0.425 |
|
| 2012 |
Kendler KS, Chen X, Dick D, Maes H, Gillespie N, Neale MC, Riley B. Recent advances in the genetic epidemiology and molecular genetics of substance use disorders. Nature Neuroscience. 15: 181-9. PMID 22281715 DOI: 10.1038/Nn.3018 |
0.321 |
|
| 2012 |
Reimers MA, Riley BP, Kalsi G, Kertes DA, Kendler KS. Pathway based analysis of genotypes in relation to alcohol dependence. The Pharmacogenomics Journal. 12: 342-8. PMID 21468025 DOI: 10.1038/Tpj.2011.10 |
0.417 |
|
| 2011 |
Bigdeli TB, Maher BS, Zhao Z, Oord EJ, Thiselton DL, Sun J, Webb BT, Amdur RL, Wormley B, O'Neill FA, Walsh D, Riley BP, Kendler KS, Fanous AH. Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness. Plos One. 6: e21440. PMID 22220189 DOI: 10.1371/Journal.Pone.0021440 |
0.463 |
|
| 2011 |
Chen YC, Prescott CA, Walsh D, Patterson DG, Riley BP, Kendler KS, Kuo PH. Different phenotypic and genotypic presentations in alcohol dependence: age at onset matters. Journal of Studies On Alcohol and Drugs. 72: 752-62. PMID 21906503 DOI: 10.15288/Jsad.2011.72.752 |
0.403 |
|
| 2011 |
Dick DM, Latendresse SJ, Riley B. Incorporating genetics into your studies: a guide for social scientists. Frontiers in Psychiatry. 2: 17. PMID 21629842 DOI: 10.3389/Fpsyt.2011.00017 |
0.37 |
|
| 2011 |
Maher BS, Vladimirov VI, Latendresse SJ, Thiselton DL, McNamee R, Kang M, Bigdeli TB, Chen X, Riley BP, Hettema JM, Chilcoat H, Heidbreder C, Muglia P, Murrelle EL, Dick DM, et al. The AVPR1A gene and substance use disorders: association, replication, and functional evidence. Biological Psychiatry. 70: 519-27. PMID 21514569 DOI: 10.1016/J.Biopsych.2011.02.023 |
0.409 |
|
| 2011 |
Sun J, Wan C, Jia P, Fanous AH, Kendler KS, Riley BP, Zhao Z. Application of systems biology approach identifies and validates GRB2 as a risk gene for schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 125: 201-8. PMID 21195589 DOI: 10.1016/J.Schres.2010.12.002 |
0.426 |
|
| 2011 |
Kertes DA, Kalsi G, Prescott CA, Kuo PH, Patterson DG, Walsh D, Kendler KS, Riley BP. Neurotransmitter and neuromodulator genes associated with a history of depressive symptoms in individuals with alcohol dependence. Alcoholism, Clinical and Experimental Research. 35: 496-505. PMID 21143246 DOI: 10.1111/J.1530-0277.2010.01366.X |
0.378 |
|
| 2011 |
Hack LM, Kalsi G, Aliev F, Kuo PH, Prescott CA, Patterson DG, Walsh D, Dick DM, Riley BP, Kendler KS. Limited associations of dopamine system genes with alcohol dependence and related traits in the Irish Affected Sib Pair Study of Alcohol Dependence (IASPSAD). Alcoholism, Clinical and Experimental Research. 35: 376-85. PMID 21083670 DOI: 10.1111/J.1530-0277.2010.01353.X |
0.479 |
|
| 2011 |
Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, ... ... Riley B, et al. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry. 16: 429-41. PMID 20368704 DOI: 10.1038/Mp.2010.36 |
0.46 |
|
| 2010 |
Kim AH, Reimers M, Maher B, Williamson V, McMichael O, McClay JL, van den Oord EJ, Riley BP, Kendler KS, Vladimirov VI. MicroRNA expression profiling in the prefrontal cortex of individuals affected with schizophrenia and bipolar disorders. Schizophrenia Research. 124: 183-91. PMID 20675101 DOI: 10.1016/J.Schres.2010.07.002 |
0.322 |
|
| 2010 |
Sun J, Jia P, Fanous AH, van den Oord E, Chen X, Riley BP, Amdur RL, Kendler KS, Zhao Z. Schizophrenia gene networks and pathways and their applications for novel candidate gene selection. Plos One. 5: e11351. PMID 20613869 DOI: 10.1371/Journal.Pone.0011351 |
0.38 |
|
| 2010 |
Dick DM, Riley B, Kendler KS. Nature and nurture in neuropsychiatric genetics: where do we stand? Dialogues in Clinical Neuroscience. 12: 7-23. PMID 20373663 |
0.331 |
|
| 2010 |
Kalsi G, Kuo PH, Aliev F, Alexander J, McMichael O, Patterson DG, Walsh D, Zhao Z, Schuckit M, Nurnberger J, Edenberg H, Kramer J, Hesselbrock V, Tischfield JA, Vladimirov V, ... ... Riley BP, et al. A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts. Human Molecular Genetics. 19: 2497-506. PMID 20332099 DOI: 10.1093/Hmg/Ddq112 |
0.487 |
|
| 2010 |
Kuo PH, Neale MC, Walsh D, Patterson DG, Riley B, Prescott CA, Kendler KS. Genome-wide linkage scans for major depression in individuals with alcohol dependence. Journal of Psychiatric Research. 44: 616-9. PMID 20074746 DOI: 10.1016/J.Jpsychires.2009.12.005 |
0.414 |
|
| 2010 |
Maher BS, Reimers MA, Riley BP, Kendler KS. Allelic heterogeneity in genetic association meta-analysis: an application to DTNBP1 and schizophrenia. Human Heredity. 69: 71-9. PMID 19996605 DOI: 10.1159/000264445 |
0.446 |
|
| 2010 |
Riley B, Thiselton D, Maher BS, Bigdeli T, Wormley B, McMichael GO, Fanous AH, Vladimirov V, O'Neill FA, Walsh D, Kendler KS. Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. Molecular Psychiatry. 15: 29-37. PMID 19844207 DOI: 10.1038/Mp.2009.109 |
0.422 |
|
| 2010 |
Fanous AH, Zhao Z, van den Oord EJ, Maher BS, Thiselton DL, Bergen SE, Wormley B, Bigdeli T, Amdur RL, O'Neill FA, Walsh D, Kendler KS, Riley BP. Association study of SNAP25 and schizophrenia in Irish family and case-control samples. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 663-74. PMID 19806613 DOI: 10.1002/Ajmg.B.31037 |
0.431 |
|
| 2010 |
Bergen SE, Fanous AH, Kuo PH, Wormley BK, O'Neill FA, Walsh D, Riley BP, Kendler KS. No association of dysbindin with symptom factors of schizophrenia in an Irish case-control sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 700-5. PMID 19760674 DOI: 10.1002/Ajmg.B.31029 |
0.376 |
|
| 2010 |
Thiselton DL, Maher BS, Webb BT, Bigdeli TB, O'Neill FA, Walsh D, Kendler KS, Riley BP. Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 323-31. PMID 19475563 DOI: 10.1002/Ajmg.B.30982 |
0.452 |
|
| 2009 |
Riley B, Kuo PH, Maher BS, Fanous AH, Sun J, Wormley B, O'Neill FA, Walsh D, Zhao Z, Kendler KS. The dystrobrevin binding protein 1 (DTNBP1) gene is associated with schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 115: 245-53. PMID 19800201 DOI: 10.1016/J.Schres.2009.09.008 |
0.431 |
|
| 2009 |
Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14: 774-85. PMID 19349958 DOI: 10.1038/Mp.2008.135 |
0.415 |
|
| 2009 |
Papavassiliou P, York TP, Gursoy N, Hill G, Nicely LV, Sundaram U, McClain A, Aggen SH, Eaves L, Riley B, Jackson-Cook C. The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues. American Journal of Medical Genetics. Part A. 149: 573-83. PMID 19291777 DOI: 10.1002/Ajmg.A.32729 |
0.306 |
|
| 2009 |
Holmans PA, Riley B, Pulver AE, Owen MJ, Wildenauer DB, Gejman PV, Mowry BJ, Laurent C, Kendler KS, Nestadt G, Williams NM, Schwab SG, Sanders AR, Nertney D, Mallet J, et al. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Molecular Psychiatry. 14: 786-95. PMID 19223858 DOI: 10.1038/Mp.2009.11 |
0.408 |
|
| 2009 |
Kuo PH, Kalsi G, Prescott CA, Hodgkinson CA, Goldman D, Alexander J, van den Oord EJ, Chen X, Sullivan PF, Patterson DG, Walsh D, Kendler KS, Riley BP. Associations of glutamate decarboxylase genes with initial sensitivity and age-at-onset of alcohol dependence in the Irish Affected Sib Pair Study of Alcohol Dependence. Drug and Alcohol Dependence. 101: 80-7. PMID 19111404 DOI: 10.1016/J.Drugalcdep.2008.11.009 |
0.428 |
|
| 2009 |
Kalsi G, Prescott CA, Kendler KS, Riley BP. Unraveling the molecular mechanisms of alcohol dependence. Trends in Genetics : Tig. 25: 49-55. PMID 19010566 DOI: 10.1016/J.Tig.2008.10.005 |
0.429 |
|
| 2009 |
Vladimirov VI, Maher BS, Wormley B, O'Neill FA, Walsh D, Kendler KS, Riley BP. The trace amine associated receptor (TAAR6) gene is not associated with schizophrenia in the Irish Case-Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 107: 249-54. PMID 18973992 DOI: 10.1016/J.Schres.2008.09.030 |
0.408 |
|
| 2009 |
Prom-Wormley EC, Eaves LJ, Foley DL, Gardner CO, Archer KJ, Wormley BK, Maes HH, Riley BP, Silberg JL. Monoamine oxidase A and childhood adversity as risk factors for conduct disorder in females. Psychological Medicine. 39: 579-90. PMID 18752729 DOI: 10.1017/S0033291708004170 |
0.343 |
|
| 2009 |
Guo AY, Sun J, Riley BP, Thiselton DL, Kendler KS, Zhao Z. The dystrobrevin-binding protein 1 gene: features and networks. Molecular Psychiatry. 14: 18-29. PMID 18663367 DOI: 10.1038/Mp.2008.88 |
0.42 |
|
| 2008 |
Mazefsky CA, Goin-Kochel RP, Riley BP, Maes HH. Genetic and Environmental Influences on Symptom Domains in Twins and Siblings with Autism. Research in Autism Spectrum Disorders. 2: 320-331. PMID 19718281 DOI: 10.1016/J.Rasd.2007.08.002 |
0.363 |
|
| 2008 |
Maher BS, Riley BP, Kendler KS. Psychiatric genetics gets a boost. Nature Genetics. 40: 1042-4. PMID 19165917 DOI: 10.1038/Ng0908-1042 |
0.459 |
|
| 2008 |
Edwards TL, Wang X, Chen Q, Wormly B, Riley B, O'Neill FA, Walsh D, Ritchie MD, Kendler KS, Chen X. Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia. Schizophrenia Research. 106: 208-17. PMID 18804346 DOI: 10.1016/J.Schres.2008.07.022 |
0.415 |
|
| 2008 |
McClellan JM, Susser E, King MC, Rietschel M, Riley B, Zammit S. Forum: The interplay of genes and environment in psychiatric disorders. Current Opinion in Psychiatry. 21: 322-3. PMID 18520731 DOI: 10.1097/Yco.0B013E328306A77F |
0.334 |
|
| 2008 |
Hodgkinson CA, Yuan Q, Xu K, Shen PH, Heinz E, Lobos EA, Binder EB, Cubells J, Ehlers CL, Gelernter J, Mann J, Riley B, Roy A, Tabakoff B, Todd RD, et al. Addictions biology: haplotype-based analysis for 130 candidate genes on a single array. Alcohol and Alcoholism (Oxford, Oxfordshire). 43: 505-15. PMID 18477577 DOI: 10.1093/Alcalc/Agn032 |
0.426 |
|
| 2008 |
Sun J, Kuo PH, Riley BP, Kendler KS, Zhao Z. Candidate genes for schizophrenia: a survey of association studies and gene ranking. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1173-81. PMID 18361404 DOI: 10.1002/Ajmg.B.30743 |
0.42 |
|
| 2008 |
Kuo PH, Kalsi G, Prescott CA, Hodgkinson CA, Goldman D, van den Oord EJ, Alexander J, Jiang C, Sullivan PF, Patterson DG, Walsh D, Kendler KS, Riley BP. Association of ADH and ALDH genes with alcohol dependence in the Irish Affected Sib Pair Study of alcohol dependence (IASPSAD) sample. Alcoholism, Clinical and Experimental Research. 32: 785-95. PMID 18331377 DOI: 10.1111/J.1530-0277.2008.00642.X |
0.453 |
|
| 2008 |
Fanous AH, Neale MC, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS. Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families. Biological Psychiatry. 64: 121-7. PMID 18255048 DOI: 10.1016/J.Biopsych.2007.11.023 |
0.361 |
|
| 2008 |
Sullivan PF, Kuo PH, Webb BT, Neale MC, Vittum J, Furberg H, Walsh D, Patterson DG, Riley B, Prescott CA, Kendler KS. Genomewide linkage survey of nicotine dependence phenotypes. Drug and Alcohol Dependence. 93: 210-6. PMID 18023296 DOI: 10.1016/J.Drugalcdep.2007.09.015 |
0.433 |
|
| 2008 |
Goin-Kochel RP, Mazefsky CA, Riley BP. Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblings. Journal of Autism and Developmental Disorders. 38: 1019-27. PMID 17968643 DOI: 10.1007/S10803-007-0476-Z |
0.331 |
|
| 2008 |
Thiselton DL, Vladimirov VI, Kuo PH, McClay J, Wormley B, Fanous A, O'Neill FA, Walsh D, Van den Oord EJ, Kendler KS, Riley BP. AKT1 is associated with schizophrenia across multiple symptom dimensions in the Irish study of high density schizophrenia families. Biological Psychiatry. 63: 449-57. PMID 17825267 DOI: 10.1016/J.Biopsych.2007.06.005 |
0.359 |
|
| 2007 |
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Riley BP, et al. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry. 12: 1129-39, 1057. PMID 17667961 DOI: 10.1038/Sj.Mp.4002053 |
0.427 |
|
| 2007 |
Vladimirov V, Thiselton DL, Kuo PH, McClay J, Fanous A, Wormley B, Vittum J, Ribble R, Moher B, Van Den Oord E, O'Neill FA, Walsh D, Kendler KS, Riley BP. A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families Molecular Psychiatry. 12: 842-853. PMID 17505468 DOI: 10.1038/Sj.Mp.4001984 |
0.407 |
|
| 2007 |
Fanous AH, Neale MC, Gardner CO, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS. Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy. Molecular Psychiatry. 12: 958-65. PMID 17440434 DOI: 10.1038/Sj.Mp.4001996 |
0.431 |
|
| 2007 |
Kuo PH, Neale MC, Riley BP, Patterson DG, Walsh D, Prescott CA, Kendler KS. A genome-wide linkage analysis for the personality trait neuroticism in the Irish affected sib-pair study of alcohol dependence. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 463-8. PMID 17427203 DOI: 10.1002/Ajmg.B.30478 |
0.405 |
|
| 2007 |
Fanous AH, Neale MC, Webb BT, Straub RE, Amdur RL, O'Neill FA, Walsh D, Riley BP, Kendler KS. A genome-wide scan for modifier loci in schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 589-95. PMID 17262803 DOI: 10.1002/Ajmg.B.30442 |
0.429 |
|
| 2007 |
Iwata Y, Nakajima M, Yamada K, Nakamura K, Sekine Y, Tsuchiya KJ, Sugihara G, Matsuzaki H, Suda S, Suzuki K, Takei N, Mori N, Iwayama Y, Takao H, Yoshikawa T, ... Riley B, et al. Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia. Neuroscience Research. 57: 194-202. PMID 17113175 DOI: 10.1016/j.neures.2006.10.002 |
0.355 |
|
| 2006 |
Kendler KS, Kuo PH, Webb BT, Kalsi G, Neale MC, Sullivan PF, Walsh D, Patterson DG, Riley B, Prescott CA. A joint genomewide linkage analysis of symptoms of alcohol dependence and conduct disorder. Alcoholism, Clinical and Experimental Research. 30: 1972-7. PMID 17117961 DOI: 10.1111/J.1530-0277.2006.00243.X |
0.402 |
|
| 2006 |
Kuo PH, Neale MC, Riley BP, Webb BT, Sullivan PF, Vittum J, Patterson DG, Thiselton DL, van den Oord EJ, Walsh D, Kendler KS, Prescott CA. Identification of susceptibility loci for alcohol-related traits in the Irish Affected Sib Pair Study of Alcohol Dependence. Alcoholism, Clinical and Experimental Research. 30: 1807-16. PMID 17067344 DOI: 10.1111/J.1530-0277.2006.00217.X |
0.431 |
|
| 2006 |
Riley BP, Kalsi G, Kuo PH, Vladimirov V, Thiselton DL, Vittum J, Wormley B, Grotewiel MS, Patterson DG, Sullivan PF, van den Oord E, Walsh D, Kendler KS, Prescott CA. Alcohol dependence is associated with the ZNF699 gene, a human locus related to Drosophila hangover, in the Irish Affected Sib Pair Study of Alcohol Dependence (IASPSAD) sample. Molecular Psychiatry. 11: 1025-31. PMID 16940975 DOI: 10.1038/Sj.Mp.4001891 |
0.483 |
|
| 2006 |
Riley B, Kendler KS. Molecular genetic studies of schizophrenia. European Journal of Human Genetics : Ejhg. 14: 669-80. PMID 16721403 DOI: 10.1038/Sj.Ejhg.5201571 |
0.486 |
|
| 2006 |
Prescott CA, Sullivan PF, Kuo PH, Webb BT, Vittum J, Patterson DG, Thiselton DL, Myers JM, Devitt M, Halberstadt LJ, Robinson VP, Neale MC, van den Oord EJ, Walsh D, Riley BP, et al. Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4. Molecular Psychiatry. 11: 603-11. PMID 16534506 DOI: 10.1038/Sj.Mp.4001811 |
0.43 |
|
| 2006 |
FANOUS AH, van den OORD EJ, RILEY BP, AGGEN SH, NEALE MC, KENDLER KS, O’NEILL FA, WALSH D. Dr. Fanous and Colleagues Reply American Journal of Psychiatry. 163: 941-942. DOI: 10.1176/Ajp.2006.163.5.941 |
0.405 |
|
| 2005 |
Fanous AH, van den Oord EJ, Riley BP, Aggen SH, Neale MC, O'Neill FA, Walsh D, Kendler KS. Relationship between a high-risk haplotype in the DTNBP1 (dysbindin) gene and clinical features of schizophrenia. The American Journal of Psychiatry. 162: 1824-32. PMID 16199828 DOI: 10.1176/Appi.Ajp.162.10.1824 |
0.406 |
|
| 2005 |
Kendler KS, Kuhn JW, Vittum J, Prescott CA, Riley B. The interaction of stressful life events and a serotonin transporter polymorphism in the prediction of episodes of major depression: a replication. Archives of General Psychiatry. 62: 529-35. PMID 15867106 DOI: 10.1001/Archpsyc.62.5.529 |
0.353 |
|
| 2004 |
Foley DL, Eaves LJ, Wormley B, Silberg JL, Maes HH, Kuhn J, Riley B. Childhood adversity, monoamine oxidase a genotype, and risk for conduct disorder. Archives of General Psychiatry. 61: 738-44. PMID 15237086 DOI: 10.1001/Archpsyc.61.7.738 |
0.328 |
|
| 2004 |
Thiselton DL, Webb BT, Neale BM, Ribble RC, O'Neill FA, Walsh D, Riley BP, Kendler KS. No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF). Molecular Psychiatry. 9: 777-83; image 729. PMID 15197397 DOI: 10.1038/Sj.Mp.4001530 |
0.434 |
|
| 2004 |
Riley B. Linkage studies of schizophrenia. Neurotoxicity Research. 6: 17-34. PMID 15184102 DOI: 10.1007/Bf03033293 |
0.487 |
|
| 2004 |
Mowry BJ, Holmans PA, Pulver AE, Gejman PV, Riley B, Williams NM, Laurent C, Schwab SG, Wildenauer DB, Bauché S, Owen MJ, Wormley B, Sanders AR, Nestadt G, Liang KY, et al. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry. 9: 784-95. PMID 15007391 DOI: 10.1038/Sj.Mp.4001481 |
0.404 |
|
| 2003 |
van den Oord EJ, Sullivan PF, Jiang Y, Walsh D, O'Neill FA, Kendler KS, Riley BP. Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families. Molecular Psychiatry. 8: 499-510. PMID 12808430 DOI: 10.1038/sj.mp.4001263 |
0.329 |
|
| 2002 |
Riley B, Williamson M, Collier D, Wilkie H, Makoff A. A 3-Mb map of a large Segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14. Genomics. 79: 197-209. PMID 11829490 DOI: 10.1006/Geno.2002.6694 |
0.342 |
|
| 2001 |
McGuffin P, Riley B, Plomin R. Genomics and behavior. Toward behavioral genomics. Science (New York, N.Y.). 291: 1232-49. PMID 11233447 DOI: 10.1126/Science.1057264 |
0.378 |
|
| 2000 |
Riley BP, Makoff A, Mogudi-Carter M, Jenkins T, Williamson R, Collier D, Murray R. Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families. American Journal of Medical Genetics. 96: 196-201. PMID 10893497 DOI: 10.1002/(Sici)1096-8628(20000403)96:2<196::Aid-Ajmg15>3.0.Co;2-4 |
0.429 |
|
| 2000 |
Riley BP, McGuffin P. Linkage and associated studies of schizophrenia. American Journal of Medical Genetics. 97: 23-44. PMID 10813802 DOI: 10.1002/(Sici)1096-8628(200021)97:1<23::Aid-Ajmg5>3.0.Co;2-K |
0.453 |
|
| 2000 |
Riley B, Williamson R. Sane genetics for schizophrenia. Nature Medicine. 6: 253-255. PMID 10700219 DOI: 10.1038/73085 |
0.427 |
|
| 1999 |
Craddock N, Lendon C, Cichon S, Culverhouse R, Detera-Wadleigh S, Devon R, Faraone S, Foroud T, Gejman P, Leonard S, McInnis M, Owen MJ, Riley B, Armstrong C, Barden N, et al. Chromosome Workshop: chromosomes 11, 14, and 15. American Journal of Medical Genetics. 88: 244-254. PMID 10374739 DOI: 10.1002/(Sici)1096-8628(19990618)88:3<244::Aid-Ajmg7>3.0.Co;2-1 |
0.356 |
|
| 1998 |
Riley B, Mogudi-Carter M, Razali M, Sidek M, Isa M, Jenkins T, Williamson R, Collier D, Murray R. Replication of suggestive evidence linking the α7-nicotinic cholinergic receptor gene on chromosome 15gi3-q14 to schizophrenia in bantu and malay families Schizophrenia Research. 29: 130. DOI: 10.1016/S0920-9964(97)88628-8 |
0.334 |
|
| 1997 |
Riley BP, Williamson R. Non-parametric analysis of chromosome 6p24-22 marker data and schizophrenia in southern African Bantu-speaking families. Psychiatric Genetics. 7: 131-2. PMID 9323327 DOI: 10.1097/00041444-199723000-00008 |
0.351 |
|
| 1996 |
Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B, Maier W, Blackwood D, Muir W, Clair DS, Morris S, Moises HW, Yang L, Kristbjarnarson H, Helgason T, Wiese C, ... ... Riley BP, et al. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study American Journal of Medical Genetics. 67: 580-594. PMID 8950417 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<580::Aid-Ajmg11>3.0.Co;2-P |
0.362 |
|
| 1996 |
Riley B, Mogudi-Carter M, Jenkins T, Williamson R. No evidence for linkage of chromosome 22 markers to schizophrenia in Southern African Bantu‐speaking families American Journal of Medical Genetics. 67: 515-522. PMID 8950408 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<515::Aid-Ajmg2>3.0.Co;2-G |
0.42 |
|
| 1996 |
Riley BP, Tahir E, Mogudi-Carter M, Rajagopalan S, Fauré S, Weissenbach J, Jenkins T, Williamson R. Preliminary results from a linkage study of the N-methyl-D-aspartate (NMDA) receptor subunit genes in a sample of Southern African Bantu-speaking families multiply affected with schizophrenia Schizophrenia Research. 18: 167. DOI: 10.1016/0920-9964(96)85532-0 |
0.325 |
|
| 1993 |
Auburger G, Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C, Hillermann R, Lunkes A, Khati C, Stevanin G, et al. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1 Nature Genetics. 4: 295-299. PMID 8358438 DOI: 10.1038/Ng0793-295 |
0.341 |
|
| 1992 |
Buxton J, Shelbourne P, Davies J, Jones C, Tongeren TV, Aslanidis C, Jong Pd, Jansen G, Anvret M, Riley B. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature. 355: 547-548. PMID 1346924 DOI: 10.1038/355547A0 |
0.303 |
|
| 1992 |
Johnson KJ, Sander T, Hicks AA, van Marle A, Janz D, Mullan MJ, Riley BP, Darlison MG. Confirmation of the localization of the human GABAA receptor alpha 1-subunit gene (GABRA1) to distal 5q by linkage analysis. Genomics. 14: 745-8. PMID 1330891 DOI: 10.1016/S0888-7543(05)80178-8 |
0.346 |
|
| Show low-probability matches. |