| Year |
Citation |
Score |
| 2024 |
Yoo D, Rhie A, Hebbar P, Antonacci F, Logsdon GA, Solar SJ, Antipov D, Pickett BD, Safonova Y, Montinaro F, Luo Y, Malukiewicz J, Storer JM, Lin J, Sequeira AN, ... ... Schork NJ, et al. Complete sequencing of ape genomes. Biorxiv : the Preprint Server For Biology. PMID 39131277 DOI: 10.1101/2024.07.31.605654 |
0.51 |
|
| 2022 |
Bae H, Gurinovich A, Karagiannis TT, Song Z, Leshchyk A, Li M, Andersen SL, Arbeev K, Yashin A, Zmuda J, An P, Feitosa M, Giuliani C, Franceschi C, Garagnani P, ... ... Schork NJ, et al. A Genome-Wide Association Study of 2304 Extreme Longevity Cases Identifies Novel Longevity Variants. International Journal of Molecular Sciences. 24. PMID 36613555 DOI: 10.3390/ijms24010116 |
0.307 |
|
| 2020 |
Hodge RD, Miller JA, Novotny M, Kalmbach BE, Ting JT, Bakken TE, Aevermann BD, Barkan ER, Berkowitz-Cerasano ML, Cobbs C, Diez-Fuertes F, Ding SL, McCorrison J, Schork NJ, Shehata SI, et al. Transcriptomic evidence that von Economo neurons are regionally specialized extratelencephalic-projecting excitatory neurons. Nature Communications. 11: 1172. PMID 32127543 DOI: 10.1038/s41467-020-14952-3 |
0.582 |
|
| 2019 |
Deacon DC, Happe CL, Chen C, Tedeschi N, Manso AM, Li T, Dalton ND, Peng Q, Farah EN, Gu Y, Tenerelli KP, Tran VD, Chen J, Peterson KL, Schork NJ, et al. Combinatorial interactions of genetic variants in human cardiomyopathy. Nature Biomedical Engineering. 3: 147-157. PMID 30923642 DOI: 10.1038/S41551-019-0348-9 |
0.456 |
|
| 2019 |
Fan X, Wang H, Sun L, Zheng X, Yin X, Zuo X, Peng Q, Standish KA, Cheng H, Zhang Y, Wang Z, Xiao F, Yang S, Zhang X, Schork NJ. Fine mapping and subphenotyping implicates ADRA1B gene variants in psoriasis susceptibility in a Chinese population. Epigenomics. PMID 30785334 DOI: 10.2217/Epi-2018-0131 |
0.462 |
|
| 2019 |
Bergen A, Shih PB, Zeeland AS, Carland T, Bansal V, Magistretti P, Strobel C, Fichter M, Kaye W, Schork N. Whole Genome Sequence Analysis Of A Cousin Pair With Restricting Anorexia Nervosa European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.349 |
0.44 |
|
| 2018 |
Bakken TE, Hodge RD, Miller JA, Yao Z, Nguyen TN, Aevermann B, Barkan E, Bertagnolli D, Casper T, Dee N, Garren E, Goldy J, Graybuck LT, Kroll M, Lasken RS, ... ... Schork NJ, et al. Single-nucleus and single-cell transcriptomes compared in matched cortical cell types. Plos One. 13: e0209648. PMID 30586455 DOI: 10.1371/Journal.Pone.0209648 |
0.575 |
|
| 2018 |
Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, ... ... Schork NJ, et al. Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. PMID 30503783 DOI: 10.1016/J.Euroneuro.2018.10.005 |
0.319 |
|
| 2018 |
Breuer R, Mattheisen M, Frank J, Krumm B, Treutlein J, Kassem L, Strohmaier J, Herms S, Mühleisen TW, Degenhardt F, Cichon S, Nöthen MM, Karypis G, Kelsoe J, Greenwood T, ... ... Schork N, et al. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. International Journal of Bipolar Disorders. 6: 24. PMID 30415424 DOI: 10.1186/S40345-018-0132-X |
0.387 |
|
| 2018 |
Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T, Naderi E, Rose LM, Wu Y, Karlsson R, Barbalic M, Lin H, Pool R, ... ... Schork N, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics. 103: 691-706. PMID 30388399 DOI: 10.1016/J.Ajhg.2018.09.009 |
0.711 |
|
| 2018 |
Boldog E, Bakken TE, Hodge RD, Novotny M, Aevermann BD, Baka J, Bordé S, Close JL, Diez-Fuertes F, Ding SL, Faragó N, Kocsis ÁK, Kovács B, Maltzer Z, McCorrison JM, ... ... Schork NJ, et al. Transcriptomic and morphophysiological evidence for a specialized human cortical GABAergic cell type. Nature Neuroscience. PMID 30150662 DOI: 10.1038/S41593-018-0205-2 |
0.555 |
|
| 2018 |
Rangan AV, McGrouther CC, Kelsoe J, Schork N, Stahl E, Zhu Q, Krishnan A, Yao V, Troyanskaya O, Bilaloglu S, Raghavan P, Bergen S, Jureus A, Landen M. A loop-counting method for covariate-corrected low-rank biclustering of gene-expression and genome-wide association study data. Plos Computational Biology. 14: e1006105. PMID 29758032 DOI: 10.1371/Journal.Pcbi.1006105 |
0.321 |
|
| 2018 |
Caussy C, Hsu C, Lo MT, Liu A, Bettencourt R, Ajmera VH, Bassirian S, Hooker J, Sy E, Richards L, Schork N, Schnabl B, Brenner DA, Sirlin CB, Chen CH, et al. Novel link between gut-microbiome derived metabolite and shared gene-effects with hepatic steatosis and fibrosis in NAFLD. Hepatology (Baltimore, Md.). PMID 29572891 DOI: 10.1002/Hep.29892 |
0.315 |
|
| 2017 |
Boeldt DL, Cheung C, Ariniello L, Darst BF, Topol S, Schork NJ, Philis-Tsimikas A, Torkamani A, Fortmann AL, Bloss CS. Patient perspectives on whole-genome sequencing for undiagnosed diseases. Personalized Medicine. 14: 17-25. PMID 29749824 DOI: 10.2217/Pme-2016-0050 |
0.55 |
|
| 2017 |
Bakken T, Cowell L, Aevermann BD, Novotny M, Hodge R, Miller JA, Lee A, Chang I, McCorrison J, Pulendran B, Qian Y, Schork NJ, Lasken RS, Lein ES, Scheuermann RH. Cell type discovery and representation in the era of high-content single cell phenotyping. Bmc Bioinformatics. 18: 559. PMID 29322913 DOI: 10.1186/S12859-017-1977-1 |
0.545 |
|
| 2017 |
Jia P, Zhao Z, Hulgan T, Bush WS, Samuels DC, Bloss CS, Heaton RK, Ellis RJ, Schork N, Marra CM, Collier AC, Clifford DB, Gelman BB, Sacktor N, Morgello S, et al. Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28447399 DOI: 10.1002/Ajmg.B.32530 |
0.359 |
|
| 2017 |
Peng Q, Schork NJ, Wilhelmsen KC, Ehlers CL. Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28436151 DOI: 10.1002/Ajmg.B.32533 |
0.42 |
|
| 2017 |
Long T, Hicks M, Yu HC, Biggs WH, Kirkness EF, Menni C, Zierer J, Small KS, Mangino M, Messier H, Brewerton S, Turpaz Y, Perkins BA, Evans AM, Miller LA, ... ... Schork NJ, et al. Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites. Nature Genetics. PMID 28263315 DOI: 10.1038/Ng.3809 |
0.316 |
|
| 2016 |
Aevermann B, McCorrison J, Venepally P, Hodge R, Bakken T, Miller J, Novotny M, Tran DN, Diezfuertes F, Christiansen L, Zhang F, Steemers F, Lasken RS, Lein ED, Schork N, et al. PRODUCTION OF A PRELIMINARY QUALITY CONTROL PIPELINE FOR SINGLE NUCLEI RNA-SEQ AND ITS APPLICATION IN THE ANALYSIS OF CELL TYPE DIVERSITY OF POST-MORTEM HUMAN BRAIN NEOCORTEX. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 22: 564-575. PMID 27897007 |
0.555 |
|
| 2016 |
Peng Q, Schork A, Bartsch H, Lo MT, Panizzon MS, Westlye LT, Kremen WS, Jernigan TL, Le Hellard S, Steen VM, Espeseth T, Huentelman M, Håberg AK, ... ... Schork NJ, et al. Conservation of Distinct Genetically-Mediated Human Cortical Pattern. Plos Genetics. 12: e1006143. PMID 27459196 DOI: 10.1371/Journal.Pgen.1006143 |
0.434 |
|
| 2016 |
Kawakatsu T, Huang SC, Jupe F, Sasaki E, Schmitz RJ, Urich MA, Castanon R, Nery JR, Barragan C, He Y, Chen H, Dubin M, Lee CR, Wang C, Bemm F, ... ... Schork NJ, et al. Epigenomic Diversity in a Global Collection of Arabidopsis thaliana Accessions. Cell. 166: 492-505. PMID 27419873 DOI: 10.1016/J.Cell.2016.06.044 |
0.52 |
|
| 2016 |
Ehlers CL, Gizer IR, Bizon C, Slutske W, Peng Q, Schork NJ, Wilhelmsen KC. Single Nucleotide Polymorphisms in the REG-CTNNA2 region of chromosome 2 and NEIL3 associated with impulsivity in a Native American sample. Genes, Brain, and Behavior. PMID 27167163 DOI: 10.1111/Gbb.12297 |
0.483 |
|
| 2015 |
Chen CH, Peng Q, Schork AJ, Lo MT, Fan CC, Wang Y, Desikan RS, Bettella F, Hagler DJ, Westlye LT, Kremen WS, Jernigan TL, Hellard SL, ... ... Schork N, et al. Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications. 6: 7549. PMID 26189703 DOI: 10.1038/Ncomms8549 |
0.537 |
|
| 2015 |
Jernigan TL, Brown TT, Hagler DJ, Akshoomoff N, Bartsch H, Newman E, Thompson WK, Bloss CS, Murray SS, Schork N, Kennedy DN, Kuperman JM, McCabe C, Chung Y, Libiger O, et al. The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. Neuroimage. PMID 25937488 DOI: 10.1016/J.Neuroimage.2015.04.057 |
0.303 |
|
| 2015 |
Bloss CS, Zeeland AA, Topol SE, Darst BF, Boeldt DL, Erikson GA, Bethel KJ, Bjork RL, Friedman JR, Hwynn N, Patay BA, Pockros PJ, Scott ER, Simon RA, Williams GW, ... Schork NJ, et al. A genome sequencing program for novel undiagnosed diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25790160 DOI: 10.1038/Gim.2015.21 |
0.566 |
|
| 2015 |
Ament SA, Szelinger S, Glusman G, Ashworth J, Hou L, Akula N, Shekhtman T, Badner JA, Brunkow ME, Mauldin DE, Stittrich AB, Rouleau K, Detera-Wadleigh SD, Nurnberger JI, Edenberg HJ, ... ... Schork N, et al. Rare variants in neuronal excitability genes influence risk for bipolar disorder. Proceedings of the National Academy of Sciences of the United States of America. 112: 3576-81. PMID 25730879 DOI: 10.1073/Pnas.1424958112 |
0.386 |
|
| 2015 |
Pham PH, Shipman WJ, Erikson GA, Schork NJ, Torkamani A. Scripps Genome ADVISER: Annotation and Distributed Variant Interpretation SERver. Plos One. 10: e0116815. PMID 25706643 DOI: 10.1371/Journal.Pone.0116815 |
0.556 |
|
| 2015 |
Ehlers C, Peng Q, Gizer I, Bizon C, Schork N, Wilhelmsen K. SY25-2LOW COVERAGE WHOLE GENOME SEQUENCING FOR ALCOHOL AND OTHER SUBSTANCE USE- RELATED PHENOTYPES IN AN AMERICAN INDIAN SAMPLE Alcohol and Alcoholism. 50: i28.2-i28. DOI: 10.1093/Alcalc/Agv076.102 |
0.521 |
|
| 2014 |
Peng Q, Gizer IR, Libiger O, Bizon C, Wilhelmsen KC, Schork NJ, Ehlers CL. Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 673-83. PMID 25270064 DOI: 10.1002/Ajmg.B.32272 |
0.387 |
|
| 2014 |
Tewhey R, Gu B, Kelesidis T, Charlton C, Bobenchik A, Hindler J, Schork NJ, Humphries RM. Mechanisms of linezolid resistance among coagulase-negative staphylococci determined by whole-genome sequencing. Mbio. 5: e00894-14. PMID 24915435 DOI: 10.1128/Mbio.00894-14 |
0.643 |
|
| 2014 |
Bright AT, Manary MJ, Tewhey R, Arango EM, Wang T, Schork NJ, Yanow SK, Winzeler EA. A high resolution case study of a patient with recurrent Plasmodium vivax infections shows that relapses were caused by meiotic siblings. Plos Neglected Tropical Diseases. 8: e2882. PMID 24901334 DOI: 10.1371/Journal.Pntd.0002882 |
0.631 |
|
| 2014 |
Levey DF, Le-Niculescu H, Frank J, Ayalew M, Jain N, Kirlin B, Learman R, Winiger E, Rodd Z, Shekhar A, Schork N, Kiefer F, Kiefe F, Wodarz N, Müller-Myhsok B, et al. Genetic risk prediction and neurobiological understanding of alcoholism. Translational Psychiatry. 4: e391. PMID 24844177 DOI: 10.1038/Tp.2014.29 |
0.328 |
|
| 2014 |
Chen YZ, Friedman JR, Chen DH, Chan GC, Bloss CS, Hisama FM, Topol SE, Carson AR, Pham PH, Bonkowski ES, Scott ER, Lee JK, Zhang G, Oliveira G, Xu J, ... ... Schork NJ, et al. Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia. Annals of Neurology. 75: 542-9. PMID 24700542 DOI: 10.1002/Ana.24119 |
0.516 |
|
| 2014 |
Peng Q, Schork NJ. Utility of network integrity methods in therapeutic target identification. Frontiers in Genetics. 5: 12. PMID 24550933 DOI: 10.3389/Fgene.2014.00012 |
0.347 |
|
| 2014 |
Boraska V, Franklin CS, Floyd JA, Thornton LM, Huckins LM, Southam L, Rayner NW, Tachmazidou I, Klump KL, Treasure J, Lewis CM, Schmidt U, Tozzi F, Kiezebrink K, Hebebrand J, ... ... Schork NJ, et al. A genome-wide association study of anorexia nervosa. Molecular Psychiatry. 19: 1085-94. PMID 24514567 DOI: 10.1038/Mp.2013.187 |
0.384 |
|
| 2014 |
Zhang K, Huentelman MJ, Rao F, Sun EI, Corneveaux JJ, Schork AJ, Wei Z, Waalen J, Miramontes-Gonzalez JP, Hightower CM, Maihofer AX, Mahata M, Pastinen T, Ehret GB, ... Schork NJ, et al. Genetic implication of a novel thiamine transporter in human hypertension. Journal of the American College of Cardiology. 63: 1542-55. PMID 24509276 DOI: 10.1016/J.Jacc.2014.01.007 |
0.304 |
|
| 2014 |
Scott-Van Zeeland AA, Bloss CS, Tewhey R, Bansal V, Torkamani A, Libiger O, Duvvuri V, Wineinger N, Galvez L, Darst BF, Smith EN, Carson A, Pham P, Phillips T, Villarasa N, ... ... Schork NJ, et al. Evidence for the role of EPHX2 gene variants in anorexia nervosa. Molecular Psychiatry. 19: 724-32. PMID 23999524 DOI: 10.1038/Mp.2013.91 |
0.769 |
|
| 2014 |
Masternak M, Zhi X, Lamperska K, Golusinski P, Luczewski L, Schork N, Golusinski W. Genetic Biomarkers in Head and Neck Squamous Cell Carcinoma Otolaryngology–Head and Neck Surgery. 151: P167-P167. DOI: 10.1177/0194599814541629a94 |
0.307 |
|
| 2013 |
Paliwal A, Temkin AM, Kerkel K, Yale A, Yotova I, Drost N, Lax S, Nhan-Chang CL, Powell C, Borczuk A, Aviv A, Wapner R, Chen X, Nagy PL, Schork N, et al. Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation. Plos Genetics. 9: e1003622. PMID 24009515 DOI: 10.1371/Journal.Pgen.1003622 |
0.605 |
|
| 2013 |
Friese RS, Altshuler AE, Zhang K, Miramontes-Gonzalez JP, Hightower CM, Jirout ML, Salem RM, Gayen JR, Mahapatra NR, Biswas N, Cale M, Vaingankar SM, Kim HS, Courel M, Taupenot L, ... ... Schork NJ, et al. MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension. Human Molecular Genetics. 22: 3624-40. PMID 23674521 DOI: 10.1093/Hmg/Ddt213 |
0.782 |
|
| 2013 |
Schork AJ, Thompson WK, Pham P, Torkamani A, Roddey JC, Sullivan PF, Kelsoe JR, O'Donovan MC, Furberg H, Schork NJ, Andreassen OA, Dale AM. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. Plos Genetics. 9: e1003449. PMID 23637621 DOI: 10.1371/Journal.Pgen.1003449 |
0.619 |
|
| 2013 |
Darst BF, Madlensky L, Schork NJ, Topol EJ, Bloss CS. Perceptions of genetic counseling services in direct-to-consumer personal genomic testing. Clinical Genetics. 84: 335-9. PMID 23590221 DOI: 10.1111/Cge.12166 |
0.304 |
|
| 2013 |
Schmitz RJ, Schultz MD, Urich MA, Nery JR, Pelizzola M, Libiger O, Alix A, McCosh RB, Chen H, Schork NJ, Ecker JR. Patterns of population epigenomic diversity. Nature. 495: 193-8. PMID 23467092 DOI: 10.1038/Nature11968 |
0.485 |
|
| 2013 |
Gamazon ER, Badner JA, Cheng L, Zhang C, Zhang D, Cox NJ, Gershon ES, Kelsoe JR, Greenwood TA, Nievergelt CM, Chen C, McKinney R, Shilling PD, Schork NJ, Smith EN, et al. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Molecular Psychiatry. 18: 340-6. PMID 22212596 DOI: 10.1038/Mp.2011.174 |
0.302 |
|
| 2012 |
Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M. The Minnesota Center for Twin and Family Research genome-wide association study. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 15: 767-74. PMID 23363460 DOI: 10.1017/Thg.2012.62 |
0.345 |
|
| 2012 |
Butler AM, Yin X, Evans DS, Nalls MA, Smith EN, Tanaka T, Li G, Buxbaum SG, Whitsel EA, Alonso A, Arking DE, Benjamin EJ, Berenson GS, Bis JC, Chen W, ... ... Schork NJ, et al. Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circulation. Cardiovascular Genetics. 5: 639-46. PMID 23139255 DOI: 10.1161/Circgenetics.112.963991 |
0.304 |
|
| 2012 |
Torkamani A, Pham P, Libiger O, Bansal V, Zhang G, Scott-Van Zeeland AA, Tewhey R, Topol EJ, Schork NJ. Clinical implications of human population differences in genome-wide rates of functional genotypes. Frontiers in Genetics. 3: 211. PMID 23125845 DOI: 10.3389/Fgene.2012.00211 |
0.756 |
|
| 2012 |
Zapala MA, Schork NJ. Statistical properties of multivariate distance matrix regression for high-dimensional data analysis. Frontiers in Genetics. 3: 190. PMID 23060897 DOI: 10.3389/Fgene.2012.00190 |
0.656 |
|
| 2012 |
Verma-Gaur J, Torkamani A, Schaffer L, Head SR, Schork NJ, Feeney AJ. Noncoding transcription within the Igh distal V(H) region at PAIR elements affects the 3D structure of the Igh locus in pro-B cells. Proceedings of the National Academy of Sciences of the United States of America. 109: 17004-9. PMID 23027941 DOI: 10.1073/Pnas.1208398109 |
0.513 |
|
| 2012 |
Tewhey R, Cannavino CR, Leake JA, Bansal V, Topol EJ, Torkamani A, Bradley JS, Schork NJ. Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300. Bmc Genomics. 13: 508. PMID 23009684 DOI: 10.1186/1471-2164-13-508 |
0.728 |
|
| 2012 |
Mangino M, Hwang SJ, Spector TD, Hunt SC, Kimura M, Fitzpatrick AL, Christiansen L, Petersen I, Elbers CC, Harris T, Chen W, Srinivasan SR, Kark JD, Benetos A, El Shamieh S, ... ... Schork NJ, et al. Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Human Molecular Genetics. 21: 5385-94. PMID 23001564 DOI: 10.1093/Hmg/Dds382 |
0.302 |
|
| 2012 |
Humphries RM, Kelesidis T, Tewhey R, Rose WE, Schork N, Nizet V, Sakoulas G. Genotypic and phenotypic evaluation of the evolution of high-level daptomycin nonsusceptibility in vancomycin-resistant Enterococcus faecium. Antimicrobial Agents and Chemotherapy. 56: 6051-3. PMID 22948885 DOI: 10.1128/Aac.01318-12 |
0.676 |
|
| 2012 |
Mei H, Chen W, Mills K, He J, Srinivasan SR, Schork N, Murray S, Berenson GS. Influences of FTO gene on onset age of adult overweight. Human Genetics. 131: 1851-9. PMID 22842737 DOI: 10.1007/S00439-012-1204-0 |
0.315 |
|
| 2012 |
Bright AT, Tewhey R, Abeles S, Chuquiyauri R, Llanos-Cuentas A, Ferreira MU, Schork NJ, Vinetz JM, Winzeler EA. Whole genome sequencing analysis of Plasmodium vivax using whole genome capture. Bmc Genomics. 13: 262. PMID 22721170 DOI: 10.1186/1471-2164-13-262 |
0.67 |
|
| 2012 |
Chow ML, Pramparo T, Winn ME, Barnes CC, Li HR, Weiss L, Fan JB, Murray S, April C, Belinson H, Fu XD, Wynshaw-Boris A, Schork NJ, Courchesne E. Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. Plos Genetics. 8: e1002592. PMID 22457638 DOI: 10.1371/Journal.Pgen.1002592 |
0.694 |
|
| 2012 |
Chow ML, Winn ME, Li HR, April C, Wynshaw-Boris A, Fan JB, Fu XD, Courchesne E, Schork NJ. Preprocessing and Quality Control Strategies for Illumina DASL Assay-Based Brain Gene Expression Studies with Semi-Degraded Samples. Frontiers in Genetics. 3: 11. PMID 22375143 DOI: 10.3389/Fgene.2012.00011 |
0.658 |
|
| 2012 |
Mei H, Chen W, Jiang F, He J, Srinivasan S, Smith EN, Schork N, Murray S, Berenson GS. Longitudinal replication studies of GWAS risk SNPs influencing body mass index over the course of childhood and adulthood. Plos One. 7: e31470. PMID 22355368 DOI: 10.1371/Journal.Pone.0031470 |
0.35 |
|
| 2012 |
Bakken TE, Roddey JC, Djurovic S, Akshoomoff N, Amaral DG, Bloss CS, Casey BJ, Chang L, Ernst TM, Gruen JR, Jernigan TL, Kaufmann WE, Kenet T, Kennedy DN, Kuperman JM, ... ... Schork NJ, et al. Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Proceedings of the National Academy of Sciences of the United States of America. 109: 3985-90. PMID 22343285 DOI: 10.1073/Pnas.1105829109 |
0.621 |
|
| 2012 |
Aoki-Ota M, Torkamani A, Ota T, Schork N, Nemazee D. Skewed primary Igκ repertoire and V-J joining in C57BL/6 mice: implications for recombination accessibility and receptor editing. Journal of Immunology (Baltimore, Md. : 1950). 188: 2305-15. PMID 22287713 DOI: 10.4049/Jimmunol.1103484 |
0.568 |
|
| 2012 |
Torkamani A, Schork NJ. Background gene expression networks significantly enhance drug response prediction by transcriptional profiling. The Pharmacogenomics Journal. 12: 446-52. PMID 21826086 DOI: 10.1038/Tpj.2011.35 |
0.533 |
|
| 2012 |
Friedman AJ, Torkamani A, Verkhivker G, Schork NJ. From coding variant to structure and function insight Proteomics Research Journal. 3: 395-405. |
0.5 |
|
| 2011 |
Le-Niculescu H, Balaraman Y, Patel SD, Ayalew M, Gupta J, Kuczenski R, Shekhar A, Schork N, Geyer MA, Niculescu AB. Convergent functional genomics of anxiety disorders: translational identification of genes, biomarkers, pathways and mechanisms. Translational Psychiatry. 1: e9. PMID 22832404 DOI: 10.1038/Tp.2011.9 |
0.372 |
|
| 2011 |
Sebastiani P, Riva A, Montano M, Pham P, Torkamani A, Scherba E, Benson G, Milton JN, Baldwin CT, Andersen S, Schork NJ, Steinberg MH, Perls TT. Whole genome sequences of a male and female supercentenarian, ages greater than 114 years. Frontiers in Genetics. 2: 90. PMID 22303384 DOI: 10.3389/Fgene.2011.00090 |
0.591 |
|
| 2011 |
Schmitz RJ, Schultz MD, Lewsey MG, O'Malley RC, Urich MA, Libiger O, Schork NJ, Ecker JR. Transgenerational epigenetic instability is a source of novel methylation variants. Science (New York, N.Y.). 334: 369-73. PMID 21921155 DOI: 10.1126/Science.1212959 |
0.431 |
|
| 2011 |
Chow ML, Li HR, Winn ME, April C, Barnes CC, Wynshaw-Boris A, Fan JB, Fu XD, Courchesne E, Schork NJ. Genome-wide expression assay comparison across frozen and fixed postmortem brain tissue samples. Bmc Genomics. 12: 449. PMID 21906392 DOI: 10.1186/1471-2164-12-449 |
0.648 |
|
| 2011 |
Bakken TE, Dale AM, Schork NJ. A geographic cline of skull and brain morphology among individuals of European Ancestry. Human Heredity. 72: 35-44. PMID 21849792 DOI: 10.1159/000330168 |
0.63 |
|
| 2011 |
Torkamani A, Scott-Van Zeeland AA, Topol EJ, Schork NJ. Annotating individual human genomes. Genomics. 98: 233-41. PMID 21839162 DOI: 10.1016/J.Ygeno.2011.07.006 |
0.56 |
|
| 2011 |
Bakken TE, Bloss CS, Roddey JC, Joyner AH, Rimol LM, Djurovic S, Melle I, Sundet K, Agartz I, Andreassen OA, Dale AM, Schork NJ. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Archives of General Psychiatry. 68: 781-90. PMID 21810643 DOI: 10.1001/Archgenpsychiatry.2011.81 |
0.774 |
|
| 2011 |
Smith EN, Koller DL, Panganiban C, Szelinger S, Zhang P, Badner JA, Barrett TB, Berrettini WH, Bloss CS, Byerley W, Coryell W, Edenberg HJ, Foroud T, Gershon ES, Greenwood TA, ... ... Schork NJ, et al. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Plos Genetics. 7: e1002134. PMID 21738484 DOI: 10.1371/Journal.Pgen.1002134 |
0.33 |
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| 2011 |
Luo W, Schork NJ, Marschke KB, Ng SC, Hermann TW, Zhang J, Sanders JM, Tooker P, Malo N, Zapala MA, Dziewanowska ZE, Negro-Vilar A, Meglasson MD. Identification of polymorphisms associated with hypertriglyceridemia and prolonged survival induced by bexarotene in treating non-small cell lung cancer. Anticancer Research. 31: 2303-11. PMID 21737656 |
0.682 |
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| 2011 |
Degner SC, Verma-Gaur J, Wong TP, Bossen C, Iverson GM, Torkamani A, Vettermann C, Lin YC, Ju Z, Schulz D, Murre CS, Birshtein BK, Schork NJ, Schlissel MS, Riblet R, et al. CCCTC-binding factor (CTCF) and cohesin influence the genomic architecture of the Igh locus and antisense transcription in pro-B cells. Proceedings of the National Academy of Sciences of the United States of America. 108: 9566-71. PMID 21606361 DOI: 10.1073/Pnas.1019391108 |
0.512 |
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| 2011 |
Bansal V, Tewhey R, Leproust EM, Schork NJ. Efficient and cost effective population resequencing by pooling and in-solution hybridization. Plos One. 6: e18353. PMID 21479135 DOI: 10.1371/Journal.Pone.0018353 |
0.661 |
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| 2011 |
Cheng J, Torkamani A, Grover RK, Jones TM, Ruiz DI, Schork NJ, Quigley MM, Hall FW, Salomon DR, Lerner RA. Ectopic B-cell clusters that infiltrate transplanted human kidneys are clonal. Proceedings of the National Academy of Sciences of the United States of America. 108: 5560-5. PMID 21415369 DOI: 10.1073/Pnas.1101148108 |
0.504 |
|
| 2011 |
Tewhey R, Bansal V, Torkamani A, Topol EJ, Schork NJ. The importance of phase information for human genomics. Nature Reviews. Genetics. 12: 215-23. PMID 21301473 DOI: 10.1038/Nrg2950 |
0.735 |
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| 2011 |
Bansal V, Tewhey R, Topol EJ, Schork NJ. The next phase in human genetics. Nature Biotechnology. 29: 38-9. PMID 21221098 DOI: 10.1038/Nbt.1757 |
0.684 |
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| 2011 |
Bansal V, Libiger O, Torkamani A, Schork NJ. An application and empirical comparison of statistical analysis methods for associating rare variants to a complex phenotype. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 76-87. PMID 21121035 |
0.584 |
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| 2011 |
McLachlan S, Lee SM, Steele TM, Hawthorne PL, Zapala MA, Eskin E, Schork NJ, Anderson GJ, Vulpe CD. In silico QTL mapping of basal liver iron levels in inbred mouse strains. Physiological Genomics. 43: 136-47. PMID 21062905 DOI: 10.1152/Physiolgenomics.00025.2010 |
0.659 |
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| 2010 |
Kerkel K, Schupf N, Hatta K, Pang D, Salas M, Kratz A, Minden M, Murty V, Zigman WB, Mayeux RP, Jenkins EC, Torkamani A, Schork NJ, Silverman W, Croy BA, et al. Altered DNA methylation in leukocytes with trisomy 21. Plos Genetics. 6: e1001212. PMID 21124956 DOI: 10.1371/Journal.Pgen.1001212 |
0.541 |
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| 2010 |
Bhatia G, Bansal V, Harismendy O, Schork NJ, Topol EJ, Frazer K, Bafna V. A covering method for detecting genetic associations between rare variants and common phenotypes. Plos Computational Biology. 6: e1000954. PMID 20976246 DOI: 10.1371/Journal.Pcbi.1000954 |
0.329 |
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| 2010 |
Bansal V, Libiger O, Torkamani A, Schork NJ. Statistical analysis strategies for association studies involving rare variants. Nature Reviews. Genetics. 11: 773-85. PMID 20940738 DOI: 10.1038/Nrg2867 |
0.61 |
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| 2010 |
Lakatos A, Derbeneva O, Younes D, Keator D, Bakken T, Lvova M, Brandon M, Guffanti G, Reglodi D, Saykin A, Weiner M, Macciardi F, Schork N, Wallace DC, Potkin SG, et al. Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort. Neurobiology of Aging. 31: 1355-63. PMID 20538375 DOI: 10.1016/J.Neurobiolaging.2010.04.031 |
0.587 |
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| 2010 |
Winn ME, Zapala MA, Hovatta I, Risbrough VB, Lillie E, Schork NJ. The effects of globin on microarray-based gene expression analysis of mouse blood. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 268-75. PMID 20473674 DOI: 10.1007/S00335-010-9261-Y |
0.681 |
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| 2010 |
Pinheiro AP, Bulik CM, Thornton LM, Sullivan PF, Root TL, Bloss CS, Berrettini WH, Schork NJ, Kaye WH, Bergen AW, Magistretti P, Brandt H, Crawford S, Crow S, Fichter MM, et al. Association study of 182 candidate genes in anorexia nervosa. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1070-80. PMID 20468064 DOI: 10.1002/Ajmg.B.31082 |
0.308 |
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| 2010 |
Levy D, Neuhausen SL, Hunt SC, Kimura M, Hwang SJ, Chen W, Bis JC, Fitzpatrick AL, Smith E, Johnson AD, Gardner JP, Srinivasan SR, Schork N, Rotter JI, Herbig U, et al. Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. Proceedings of the National Academy of Sciences of the United States of America. 107: 9293-8. PMID 20421499 DOI: 10.1073/Pnas.0911494107 |
0.435 |
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| 2010 |
Jirout ML, Friese RS, Mahapatra NR, Mahata M, Taupenot L, Mahata SK, Kren V, ZÃdek V, Fischer J, Maatz H, Ziegler MG, Pravenec M, Hubner N, Aitman TJ, Schork NJ, et al. Genetic regulation of catecholamine synthesis, storage and secretion in the spontaneously hypertensive rat. Human Molecular Genetics. 19: 2567-80. PMID 20378607 DOI: 10.1093/Hmg/Ddq135 |
0.772 |
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| 2010 |
Torkamani A, Dean B, Schork NJ, Thomas EA. Coexpression network analysis of neural tissue reveals perturbations in developmental processes in schizophrenia. Genome Research. 20: 403-12. PMID 20197298 DOI: 10.1101/Gr.101956.109 |
0.532 |
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| 2010 |
Bansal V, Harismendy O, Tewhey R, Murray SS, Schork NJ, Topol EJ, Frazer KA. Accurate detection and genotyping of SNPs utilizing population sequencing data. Genome Research. 20: 537-45. PMID 20150320 DOI: 10.1101/Gr.100040.109 |
0.675 |
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| 2010 |
Rimol LM, Agartz I, Djurovic S, Brown AA, Roddey JC, Kähler AK, Mattingsdal M, Athanasiu L, Joyner AH, Schork NJ, Halgren E, Sundet K, Melle I, Dale AM, Andreassen OA, et al. Sex-dependent association of common variants of microcephaly genes with brain structure. Proceedings of the National Academy of Sciences of the United States of America. 107: 384-8. PMID 20080800 DOI: 10.1073/Pnas.0908454107 |
0.788 |
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| 2010 |
Lahiry P, Torkamani A, Schork NJ, Hegele RA. Kinase mutations in human disease: interpreting genotype-phenotype relationships. Nature Reviews. Genetics. 11: 60-74. PMID 20019687 DOI: 10.1038/Nrg2707 |
0.535 |
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| 2010 |
Freimer N, McCarthy M, Schork N. Leena Peltonen-Palotie: the human side of genetics Human Molecular Genetics. 19: 3303-3305. DOI: 10.1093/HMG/DDQ255 |
0.31 |
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| 2009 |
Dixit A, Yi L, Gowthaman R, Torkamani A, Schork NJ, Verkhivker GM. Sequence and structure signatures of cancer mutation hotspots in protein kinases. Plos One. 4: e7485. PMID 19834613 DOI: 10.1371/Journal.Pone.0007485 |
0.525 |
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| 2009 |
Joyner AH, J CR, Bloss CS, Bakken TE, Rimol LM, Melle I, Agartz I, Djurovic S, Topol EJ, Schork NJ, Andreassen OA, Dale AM. A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations. Proceedings of the National Academy of Sciences of the United States of America. 106: 15483-8. PMID 19717458 DOI: 10.1073/Pnas.0901866106 |
0.779 |
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| 2009 |
Torkamani A, Schork NJ. Pathway and network analysis with high-density allelic association data. Methods in Molecular Biology (Clifton, N.J.). 563: 289-301. PMID 19597792 DOI: 10.1007/978-1-60761-175-2_16 |
0.606 |
|
| 2009 |
Torkamani A, Schork NJ. Identification of rare cancer driver mutations by network reconstruction. Genome Research. 19: 1570-8. PMID 19574499 DOI: 10.1101/Gr.092833.109 |
0.525 |
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| 2009 |
Torkamani A, Schork NJ. Prestige centrality-based functional outlier detection in gene expression analysis. Bioinformatics (Oxford, England). 25: 2222-8. PMID 19549629 DOI: 10.1093/Bioinformatics/Btp388 |
0.548 |
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| 2009 |
Pawlikowska L, Hu D, Huntsman S, Sung A, Chu C, Chen J, Joyner AH, Schork NJ, Hsueh WC, Reiner AP, Psaty BM, Atzmon G, Barzilai N, Cummings SR, Browner WS, et al. Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity. Aging Cell. 8: 460-72. PMID 19489743 DOI: 10.1111/J.1474-9726.2009.00493.X |
0.776 |
|
| 2009 |
Dixit A, Torkamani A, Schork NJ, Verkhivker G. Computational modeling of structurally conserved cancer mutations in the RET and MET kinases: the impact on protein structure, dynamics, and stability. Biophysical Journal. 96: 858-74. PMID 19186126 DOI: 10.1016/J.Bpj.2008.10.041 |
0.502 |
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| 2009 |
Zhang D, Cheng L, Qian Y, Alliey-Rodriguez N, Kelsoe JR, Greenwood T, Nievergelt C, Barrett TB, McKinney R, Schork N, Smith EN, Bloss C, Nurnberger J, Edenberg HJ, Foroud T, et al. Singleton deletions throughout the genome increase risk of bipolar disorder. Molecular Psychiatry. 14: 376-80. PMID 19114987 DOI: 10.1038/Mp.2008.144 |
0.365 |
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| 2009 |
Torkamani A, Verkhivker G, Schork NJ. Cancer driver mutations in protein kinase genes. Cancer Letters. 281: 117-27. PMID 19081671 DOI: 10.1016/J.Canlet.2008.11.008 |
0.539 |
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| 2009 |
Johnson AD, Gong Y, Wang D, Langaee TY, Shin J, Cooper-Dehoff RM, Schork NJ, Binkley P, Pepine CJ, Johnson JA, Sadee W. Promoter polymorphisms in ACE (angiotensin I-converting enzyme) associated with clinical outcomes in hypertension. Clinical Pharmacology and Therapeutics. 85: 36-44. PMID 18946466 DOI: 10.1038/Clpt.2008.194 |
0.353 |
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| 2008 |
Mossé YP, Laudenslager M, Longo L, Cole KA, Wood A, Attiyeh EF, Laquaglia MJ, Sennett R, Lynch JE, Perri P, Laureys G, Speleman F, Kim C, Hou C, Hakonarson H, ... ... Schork NJ, et al. Identification of ALK as a major familial neuroblastoma predisposition gene. Nature. 455: 930-5. PMID 18724359 DOI: 10.1038/Nature07261 |
0.538 |
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| 2008 |
Torkamani A, Topol EJ, Schork NJ. Pathway analysis of seven common diseases assessed by genome-wide association. Genomics. 92: 265-72. PMID 18722519 DOI: 10.1016/J.Ygeno.2008.07.011 |
0.594 |
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| 2008 |
Torkamani A, Kannan N, Taylor SS, Schork NJ. Congenital disease SNPs target lineage specific structural elements in protein kinases. Proceedings of the National Academy of Sciences of the United States of America. 105: 9011-6. PMID 18579784 DOI: 10.1073/Pnas.0802403105 |
0.565 |
|
| 2008 |
Torkamani A, Schork NJ. Predicting functional regulatory polymorphisms. Bioinformatics (Oxford, England). 24: 1787-92. PMID 18562267 DOI: 10.1093/Bioinformatics/Btn311 |
0.575 |
|
| 2008 |
Torkamani A, Schork NJ. Prediction of cancer driver mutations in protein kinases. Cancer Research. 68: 1675-82. PMID 18339846 DOI: 10.1158/0008-5472.Can-07-5283 |
0.513 |
|
| 2008 |
Zhou D, Wang J, Zapala MA, Xue J, Schork NJ, Haddad GG. Gene expression in mouse brain following chronic hypoxia: role of sarcospan in glial cell death. Physiological Genomics. 32: 370-9. PMID 18056785 DOI: 10.1152/Physiolgenomics.00147.2007 |
0.677 |
|
| 2007 |
Torkamani A, Schork NJ. Accurate prediction of deleterious protein kinase polymorphisms. Bioinformatics (Oxford, England). 23: 2918-25. PMID 17855419 DOI: 10.1093/Bioinformatics/Btm437 |
0.58 |
|
| 2007 |
Mosley CA, Taupenot L, Biswas N, Taulane JP, Olson NH, Vaingankar SM, Wen G, Schork NJ, Ziegler MG, Mahata SK, O'Connor DT. Biogenesis of the secretory granule: chromogranin A coiled-coil structure results in unusual physical properties and suggests a mechanism for granule core condensation. Biochemistry. 46: 10999-1012. PMID 17718510 DOI: 10.1021/Bi700704R |
0.682 |
|
| 2007 |
Greenhall JA, Zapala MA, Cáceres M, Libiger O, Barlow C, Schork NJ, Lockhart DJ. Detecting genetic variation in microarray expression data. Genome Research. 17: 1228-35. PMID 17609390 DOI: 10.1101/Gr.6307307 |
0.708 |
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| 2007 |
Torkamani A, Schork NJ. Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family. Genomics. 90: 49-58. PMID 17498919 DOI: 10.1016/J.Ygeno.2007.03.006 |
0.572 |
|
| 2007 |
Wessel J, Zapala MA, Schork NJ. Accommodating pathway information in expression quantitative trait locus analysis. Genomics. 90: 132-42. PMID 17493783 DOI: 10.1016/J.Ygeno.2007.03.003 |
0.707 |
|
| 2007 |
Gu CC, Hunt SC, Kardia S, Turner ST, Chakravarti A, Schork N, Olshen R, Curb D, Jaquish C, Boerwinkle E, Rao DC. An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP). Human Genetics. 121: 577-90. PMID 17372766 DOI: 10.1007/S00439-007-0349-8 |
0.371 |
|
| 2007 |
Hovatta I, Zapala MA, Broide RS, Schadt EE, Libiger O, Schork NJ, Lockhart DJ, Barlow C. DNA variation and brain region-specific expression profiles exhibit different relationships between inbred mouse strains: implications for eQTL mapping studies. Genome Biology. 8: R25. PMID 17324278 DOI: 10.1186/Gb-2007-8-2-R25 |
0.685 |
|
| 2006 |
Zapala MA, Schork NJ. Multivariate regression analysis of distance matrices for testing associations between gene expression patterns and related variables. Proceedings of the National Academy of Sciences of the United States of America. 103: 19430-5. PMID 17146048 DOI: 10.1073/Pnas.0609333103 |
0.681 |
|
| 2005 |
Stein MB, Fallin MD, Schork NJ, Gelernter J. COMT polymorphisms and anxiety-related personality traits. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 30: 2092-102. PMID 15956988 DOI: 10.1038/sj.npp.1300787 |
0.529 |
|
| 2005 |
Jorgenson E, Tang H, Gadde M, Province M, Leppert M, Kardia S, Schork N, Cooper R, Rao DC, Boerwinkle E, Risch N. Ethnicity and human genetic linkage maps. American Journal of Human Genetics. 76: 276-90. PMID 15627237 DOI: 10.1086/427926 |
0.352 |
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| 2004 |
Conti LH, Jirout M, Breen L, Vanella JJ, Schork NJ, Printz MP. Identification of quantitative trait Loci for anxiety and locomotion phenotypes in rat recombinant inbred strains. Behavior Genetics. 34: 93-103. PMID 14739700 DOI: 10.1023/B:Bege.0000009479.02183.1F |
0.779 |
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| 2003 |
Jirout M, Krenová D, Kren V, Breen L, Pravenec M, Schork NJ, Printz MP. A new framework marker-based linkage map and SDPs for the rat HXB/BXH strain set. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 537-46. PMID 12925886 DOI: 10.1007/S00335-003-2266-Z |
0.773 |
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| 2002 |
Schork NJ, Gardner JP, Zhang L, Fallin D, Thiel B, Jakubowski H, Aviv A. Genomic association/linkage of sodium lithium countertransport in CEPH pedigrees. Hypertension. 40: 619-28. PMID 12411453 DOI: 10.1161/01.HYP.0000037131.41957.A8 |
0.304 |
|
| 2001 |
Schork NJ. Genome partitioning and whole-genome analysis. Advances in Genetics. 42: 299-322. PMID 11037329 DOI: 10.1016/S0065-2660(01)42030-X |
0.305 |
|
| 1999 |
Xu X, Yang J, Rogus J, Chen C, Schork N, Xu X. Mapping of a Blood Pressure Quantitative Trait Locus to Chromosome 15q in a Chinese Population Human Molecular Genetics. 8: 2551-2555. PMID 10556304 DOI: 10.1093/Hmg/8.13.2551 |
0.346 |
|
| 1999 |
Drazen JM, Yandava CN, Dubé L, Szczerback N, Hippensteel R, Pillari A, Israel E, Schork N, Silverman ES, Katz DA, Drajesk J. Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment Nature Genetics. 22: 168-170. PMID 10369259 DOI: 10.1038/9680 |
0.313 |
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| 1999 |
Niu T, Chen C, Yang J, Wang B, Wang Z, Schork N, Fang Z, Xu X. Blood pressure and the T174M and M235T polymorphisms of the angiotensinogen gene Annals of Epidemiology. 9: 245-253. PMID 10332930 DOI: 10.1016/S1047-2797(98)00060-X |
0.336 |
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