| Year |
Citation |
Score |
| 2022 |
Highland HM, Wojcik GL, Graff M, Nishimura KK, Hodonsky CJ, Baldassari AR, Cote AC, Cheng I, Gignoux CR, Tao R, Li Y, Boerwinkle E, Fornage M, Haessler J, Hindorff LA, ... ... Matise TC, et al. Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits. American Journal of Human Genetics. PMID 35263625 DOI: 10.1016/j.ajhg.2022.02.013 |
0.303 |
|
| 2020 |
Abel HJ, Larson DE, Regier AA, Chiang C, Das I, Kanchi KL, Layer RM, Neale BM, Salerno WJ, Reeves C, Buyske S, Matise TC, Muzny DM, Zody MC, et al. Mapping and characterization of structural variation in 17,795 human genomes. Nature. PMID 32460305 DOI: 10.1038/s41586-020-2371-0 |
0.312 |
|
| 2020 |
Hu Y, Graff M, Haessler J, Buyske S, Bien SA, Tao R, Highland HM, Nishimura KK, Zubair N, Lu Y, Verbanck M, Hilliard AT, Klarin D, Damrauer SM, Ho YL, ... ... Matise TC, et al. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Plos Genetics. 16: e1008684. PMID 32226016 DOI: 10.1371/journal.pgen.1008684 |
0.369 |
|
| 2020 |
Highland HM, Downie C, Dimos SF, Graff M, Polfus LM, Darst BF, Baldassari ARM, Sitlani C, Howard AG, Kooperberg CL, Loos R, Matise T, Mottl AK, North KE, Avery CL. 198-LB: Pleiotropy Analysis of Adiposity, Glycemic, and Renal Traits in the Population Architecture Using Genomics in Epidemiology (PAGE) Consortium Diabetes. 69. DOI: 10.2337/Db20-198-Lb |
0.346 |
|
| 2019 |
Pendergrass SA, Buyske S, Jeff JM, Frase A, Dudek S, Bradford Y, Ambite JL, Avery CL, Buzkova P, Deelman E, Fesinmeyer MD, Haiman C, Heiss G, Hindorff LA, Hsu CN, ... ... Matise TC, et al. A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans. Plos One. 14: e0226771. PMID 31891604 DOI: 10.1371/Journal.Pone.0226771 |
0.468 |
|
| 2019 |
Wojcik GL, Graff M, Nishimura KK, Tao R, Haessler J, Gignoux CR, Highland HM, Patel YM, Sorokin EP, Avery CL, Belbin GM, Bien SA, Cheng I, Cullina S, Hodonsky CJ, ... ... Matise TC, et al. Genetic analyses of diverse populations improves discovery for complex traits. Nature. PMID 31217584 DOI: 10.1038/S41586-019-1310-4 |
0.425 |
|
| 2019 |
Lin BM, Nadkarni GN, Tao R, Graff M, Fornage M, Buyske S, Matise TC, Highland HM, Wilkens LR, Carlson CS, Park SL, Setiawan VW, Ambite JL, Heiss G, Boerwinkle E, et al. Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study. Frontiers in Genetics. 10: 494. PMID 31178898 DOI: 10.3389/Fgene.2019.00494 |
0.383 |
|
| 2019 |
Bien SA, Wojcik GL, Hodonsky CJ, Gignoux CR, Cheng I, Matise TC, Peters U, Kenny EE, North KE. The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE. Annual Review of Genomics and Human Genetics. PMID 30978304 DOI: 10.1146/Annurev-Genom-091416-035517 |
0.428 |
|
| 2019 |
Posey JE, O'Donnell-Luria AH, Chong JX, Harel T, Jhangiani SN, Coban Akdemir ZH, Buyske S, Pehlivan D, Carvalho CMB, Baxter S, Sobreira N, Liu P, Wu N, Rosenfeld JA, Kumar S, ... ... Matise TC, et al. Insights into genetics, human biology and disease gleaned from family based genomic studies. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30655598 DOI: 10.1038/S41436-018-0408-7 |
0.434 |
|
| 2018 |
Regier AA, Farjoun Y, Larson DE, Krasheninina O, Kang HM, Howrigan DP, Chen BJ, Kher M, Banks E, Ames DC, English AC, Li H, Xing J, Zhang Y, Matise T, et al. Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. Nature Communications. 9: 4038. PMID 30279509 DOI: 10.1038/S41467-018-06159-4 |
0.378 |
|
| 2018 |
Fernández-Rhodes L, Malinowski JR, Wang Y, Tao R, Pankratz N, Jeff JM, Yoneyama S, Carty CL, Setiawan VW, Le Marchand L, Haiman C, Corbett S, Demerath E, Heiss G, Gross M, ... ... Matise T, et al. The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis. Plos One. 13: e0200486. PMID 30044860 DOI: 10.1371/Journal.Pone.0200486 |
0.417 |
|
| 2017 |
Gong J, Nishimura KK, Fernandez-Rhodes L, Haessler J, Bien S, Graff M, Lim U, Lu Y, Gross M, Fornage M, Yoneyama S, Isasi CR, Buzkova P, Daviglus M, Lin DY, ... ... Matise TC, et al. Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI. International Journal of Obesity (2005). PMID 29381148 DOI: 10.1038/Ijo.2017.304 |
0.35 |
|
| 2017 |
Bien SA, Pankow JS, Haessler J, Lu Y, Pankratz N, Rohde RR, Tamuno A, Carlson CS, Schumacher FR, Bůžková P, Daviglus ML, Lim U, Fornage M, Fernandez-Rhodes L, Avilés-Santa L, ... ... Matise TC, et al. Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID 29038867 DOI: 10.1007/S00125-017-4476-Z |
0.469 |
|
| 2017 |
Bien SA, Pankow JS, Haessler J, Lu YN, Pankratz N, Rohde RR, Tamuno A, Carlson CS, Schumacher FR, Bůžková P, Daviglus ML, Lim U, Fornage M, Fernandez-Rhodes L, Avilés-Santa L, ... ... Matise TC, et al. Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID 28905132 DOI: 10.1007/S00125-017-4405-1 |
0.462 |
|
| 2017 |
Fernández-Rhodes L, Gong J, Haessler J, Franceschini N, Graff M, Nishimura KK, Wang Y, Highland HM, Yoneyama S, Bush WS, Goodloe R, Ritchie MD, Crawford D, Gross M, Fornage M, ... ... Matise TC, et al. Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci. Human Genetics. PMID 28391526 DOI: 10.1007/S00439-017-1787-6 |
0.482 |
|
| 2016 |
Bien SA, Wojcik GL, Zubair N, Gignoux CR, Martin AR, Kocarnik JM, Martin LW, Buyske S, Haessler J, Walker RW, Cheng I, Graff M, Xia L, Franceschini N, Matise T, et al. Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array. Plos One. 11: e0167758. PMID 27973554 DOI: 10.1371/Journal.Pone.0167758 |
0.441 |
|
| 2016 |
Yoneyama S, Yao J, Guo X, Fernandez-Rhodes L, Lim U, Boston J, Buzková P, Carlson CS, Cheng I, Cochran B, Cooper R, Ehret G, Fornage M, Gong J, Gross M, ... ... Matise TC, et al. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations. International Journal of Obesity (2005). PMID 27867202 DOI: 10.1038/Ijo.2016.207 |
0.415 |
|
| 2015 |
Kocarnik JM, Park SL, Han J, Dumitrescu L, Cheng I, Wilkens LR, Schumacher FR, Kolonel L, Carlson CS, Crawford DC, Goodloe RJ, Dilks HH, Baker P, Richardson D, Matise TC, et al. Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study. Plos One. 10: e0120491. PMID 25789475 DOI: 10.1371/Journal.Pone.0120491 |
0.372 |
|
| 2015 |
Li BI, Matteson PG, Ababon MF, Nato AQ, Lin Y, Nanda V, Matise TC, Millonig JH. The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation. Developmental Biology. 402: 17-31. PMID 25753732 DOI: 10.1016/J.Ydbio.2015.02.007 |
0.702 |
|
| 2015 |
Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH, Fischer K, Justice AE, Workalemahu T, Wu JM, Buchkovich ML, Heard-Costa NL, Roman TS, ... ... Matise TC, et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 518: 187-96. PMID 25673412 DOI: 10.1038/Nature14132 |
0.351 |
|
| 2014 |
Musolf A, Nato AQ, Londono D, Zhou L, Matise TC, Gordon D. Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. Bmc Proceedings. 8: S81. PMID 25519410 DOI: 10.1186/1753-6561-8-S1-S81 |
0.749 |
|
| 2014 |
Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J, Kutalik Z, Amin N, Buchkovich ML, Croteau-Chonka DC, Day FR, Duan Y, ... ... Matise TC, et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics. 46: 1173-86. PMID 25282103 DOI: 10.1038/Ng.3097 |
0.404 |
|
| 2014 |
Restrepo NA, Spencer KL, Goodloe R, Garrett TA, Heiss G, Bůžková P, Jorgensen N, Jensen RA, Matise TC, Hindorff LA, Klein BE, Klein R, Wong TY, Cheng CY, Cornes BK, et al. Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study. Investigative Ophthalmology & Visual Science. 55: 6839-50. PMID 25205864 DOI: 10.1167/Iovs.14-14246 |
0.344 |
|
| 2014 |
Park SL, Caberto CP, Lin Y, Goodloe RJ, Dumitrescu L, Love SA, Matise TC, Hindorff LA, Fowke JH, Schumacher FR, Beebe-Dimmer J, Chen C, Hou L, Thomas F, Deelman E, et al. Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 23: 2568-78. PMID 25139936 DOI: 10.1158/1055-9965.Epi-14-0129 |
0.342 |
|
| 2014 |
Lim U, Kocarnik JM, Bush WS, Matise TC, Caberto C, Park SL, Carlson CS, Deelman E, Duggan D, Fesinmeyer M, Haiman CA, Henderson BE, Hindorff LA, Kolonel LN, Peters U, et al. Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium. Plos One. 9: e89791. PMID 24598796 DOI: 10.1371/Journal.Pone.0089791 |
0.366 |
|
| 2013 |
Gong J, Schumacher F, Lim U, Hindorff LA, Haessler J, Buyske S, Carlson CS, Rosse S, Bůžková P, Fornage M, Gross M, Pankratz N, Pankow JS, Schreiner PJ, Cooper R, ... ... Matise TC, et al. Fine Mapping and Identification of BMI Loci in African Americans. American Journal of Human Genetics. 93: 661-71. PMID 24094743 DOI: 10.1016/J.Ajhg.2013.08.012 |
0.498 |
|
| 2013 |
Carlson CS, Matise TC, North KE, Haiman CA, Fesinmeyer MD, Buyske S, Schumacher FR, Peters U, Franceschini N, Ritchie MD, Duggan DJ, Spencer KL, Dumitrescu L, Eaton CB, Thomas F, et al. Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study. Plos Biology. 11: e1001661. PMID 24068893 DOI: 10.1371/Journal.Pbio.1001661 |
0.402 |
|
| 2013 |
Duan Q, Liu EY, Auer PL, Zhang G, Lange EM, Jun G, Bizon C, Jiao S, Buyske S, Franceschini N, Carlson CS, Hsu L, Reiner AP, Peters U, Haessler J, ... ... Matise TC, et al. Imputation of coding variants in African Americans: better performance using data from the exome sequencing project. Bioinformatics (Oxford, England). 29: 2744-9. PMID 23956302 DOI: 10.1093/Bioinformatics/Btt477 |
0.331 |
|
| 2013 |
Fesinmeyer MD, North KE, Ritchie MD, Lim U, Franceschini N, Wilkens LR, Gross MD, Bůžková P, Glenn K, Quibrera PM, Fernández-Rhodes L, Li Q, Fowke JH, Li R, Carlson CS, ... ... Matise TC, et al. Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study. Obesity (Silver Spring, Md.). 21: 835-46. PMID 23712987 DOI: 10.1002/Oby.20268 |
0.359 |
|
| 2013 |
Zhang L, Buzkova P, Wassel CL, Roman MJ, North KE, Crawford DC, Boston J, Brown-Gentry KD, Cole SA, Deelman E, Goodloe R, Wilson S, Heiss G, Jenny NS, Jorgensen NW, ... Matise TC, et al. Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study. Atherosclerosis. 228: 390-9. PMID 23587283 DOI: 10.1016/J.Atherosclerosis.2013.02.038 |
0.73 |
|
| 2013 |
Wu Y, Waite LL, Jackson AU, Sheu WH, Buyske S, Absher D, Arnett DK, Boerwinkle E, Bonnycastle LL, Carty CL, Cheng I, Cochran B, Croteau-Chonka DC, Dumitrescu L, Eaton CB, ... ... Matise TC, et al. Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. Plos Genetics. 9: e1003379. PMID 23555291 DOI: 10.1371/Journal.Pgen.1003379 |
0.433 |
|
| 2013 |
Zhang L, Spencer KL, Voruganti VS, Jorgensen NW, Fornage M, Best LG, Brown-Gentry KD, Cole SA, Crawford DC, Deelman E, Franceschini N, Gaffo AL, Glenn KR, Heiss G, Jenny NS, ... ... Matise TC, et al. Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study. American Journal of Epidemiology. 177: 923-32. PMID 23552988 DOI: 10.1093/Aje/Kws330 |
0.303 |
|
| 2013 |
Carty CL, Spencer KL, Setiawan VW, Fernandez-Rhodes L, Malinowski J, Buyske S, Young A, Jorgensen NW, Cheng I, Carlson CS, Brown-Gentry K, Goodloe R, Park A, Parikh NI, Henderson B, ... ... Matise TC, et al. Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study. Human Reproduction (Oxford, England). 28: 1695-706. PMID 23508249 DOI: 10.1093/Humrep/Det071 |
0.396 |
|
| 2013 |
Londono D, Chen KM, Musolf A, Wang R, Shen T, Brandon J, Herring JA, Wise CA, Zou H, Jin M, Yu L, Finch SJ, Matise TC, Gordon D. A novel method for analyzing genetic association with longitudinal phenotypes. Statistical Applications in Genetics and Molecular Biology. 12: 241-61. PMID 23502345 DOI: 10.1515/Sagmb-2012-0070 |
0.432 |
|
| 2013 |
Spencer KL, Malinowski J, Carty CL, Franceschini N, Fernández-Rhodes L, Young A, Cheng I, Ritchie MD, Haiman CA, Wilkens L, Chunyuanwu, Matise TC, Carlson CS, Brennan K, Park A, et al. Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study. Plos One. 8: e55258. PMID 23424626 DOI: 10.1371/Journal.Pone.0055258 |
0.412 |
|
| 2013 |
Pendergrass SA, Brown-Gentry K, Dudek S, Frase A, Torstenson ES, Goodloe R, Ambite JL, Avery CL, Buyske S, Bůžková P, Deelman E, Fesinmeyer MD, Haiman CA, Heiss G, Hindorff LA, ... ... Matise TC, et al. Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network. Plos Genetics. 9: e1003087. PMID 23382687 DOI: 10.1371/Journal.Pgen.1003087 |
0.457 |
|
| 2013 |
Peters U, North KE, Sethupathy P, Buyske S, Haessler J, Jiao S, Fesinmeyer MD, Jackson RD, Kuller LH, Rajkovic A, Lim U, Cheng I, Schumacher F, Wilkens L, Li R, ... ... Matise TC, et al. A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. Plos Genetics. 9: e1003171. PMID 23341774 DOI: 10.1371/Journal.Pgen.1003171 |
0.478 |
|
| 2012 |
Kim W, Londono D, Zhou L, Xing J, Nato AQ, Musolf A, Matise TC, Finch SJ, Gordon D. Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error. Human Heredity. 74: 172-83. PMID 23594495 DOI: 10.1159/000346824 |
0.729 |
|
| 2012 |
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, Carlson C, Carty C, Crawford DC, Haessler J, Hindorff LA, Marchand LL, Manolio TA, Matise T, Wang W, Kooperberg C, et al. Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative. Genetic Epidemiology. 36: 107-17. PMID 22851474 DOI: 10.1002/Gepi.21603 |
0.404 |
|
| 2012 |
Buyske S, Wu Y, Carty CL, Cheng I, Assimes TL, Dumitrescu L, Hindorff LA, Mitchell S, Ambite JL, Boerwinkle E, Buzkova P, Carlson CS, Cochran B, Duggan D, Eaton CB, ... ... Matise TC, et al. Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. Plos One. 7: e35651. PMID 22539988 DOI: 10.1371/Journal.Pone.0035651 |
0.47 |
|
| 2012 |
Carty CL, Buzková P, Fornage M, Franceschini N, Cole S, Heiss G, Hindorff LA, Howard BV, Mann S, Martin LW, Zhang Y, Matise TC, Prentice R, Reiner AP, Kooperberg C. Associations between incident ischemic stroke events and stroke and cardiovascular disease-related genome-wide association studies single nucleotide polymorphisms in the Population Architecture Using Genomics and Epidemiology study. Circulation. Cardiovascular Genetics. 5: 210-6. PMID 22403240 DOI: 10.1161/Circgenetics.111.962191 |
0.347 |
|
| 2012 |
Perdry H, Müller-Myhsok B, Clerget-Darpoux F, Génin E, Sahbatou M, Kim W, Londono D, Kazma R, Cardin NJ, Witte JS, Asimit JL, Zeggini E, Jouan L, Gauthier J, Dion PA, ... ... Matise TC, et al. Contents Vol. 74, 2012 Human Heredity. 74. DOI: 10.1159/000346894 |
0.666 |
|
| 2012 |
Fesinmeyer MD, Lin Y, Biggs ML, Bush WS, Butler AM, Buyske S, Caberto CP, Carty CL, Cote ML, Crawford DC, Dumitrescu L, Fowke JH, Giovino GA, Haiman CA, Heiss G, ... ... Matise TC, et al. Abstract 1662: Pleiotropic effects on lung cancer of genetic susceptibility variants identified for other malignancies: The Population Architecture using Genomics and Epidemiology Study Cancer Research. 72: 1662-1662. DOI: 10.1158/1538-7445.Am2012-1662 |
0.357 |
|
| 2012 |
Fesinmeyer MD, North KE, Ritchie MD, Lim U, Franceschini N, Wilkens LR, Gross MD, Bůžková P, Glenn K, Quibrera PM, Fernández-Rhodes L, Li Q, Fowke JH, Li R, Carlson CS, ... ... Matise TC, et al. Genetic Risk Factors for BMI and Obesity in an Ethnically Diverse Population: Results From the Population Architecture Using Genomics and Epidemiology (PAGE) Study Obesity. DOI: 10.1038/Oby.2012.158 |
0.344 |
|
| 2011 |
Matise TC, Ambite JL, Buyske S, Carlson CS, Cole SA, Crawford DC, Haiman CA, Heiss G, Kooperberg C, Marchand LL, Manolio TA, North KE, Peters U, Ritchie MD, Hindorff LA, et al. The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. American Journal of Epidemiology. 174: 849-59. PMID 21836165 DOI: 10.1093/Aje/Kwr160 |
0.466 |
|
| 2011 |
Pendergrass SA, Brown-Gentry K, Dudek SM, Torstenson ES, Ambite JL, Avery CL, Buyske S, Cai C, Fesinmeyer MD, Haiman C, Heiss G, Hindorff LA, Hsu CN, Jackson RD, Kooperberg C, ... ... Matise TC, et al. The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery. Genetic Epidemiology. 35: 410-22. PMID 21594894 DOI: 10.1002/Gepi.20589 |
0.417 |
|
| 2011 |
He C, Weeks DE, Buyske S, Abecasis GR, Stewart WC, Matise TC. Enhanced genetic maps from family-based disease studies: population-specific comparisons. Bmc Medical Genetics. 12: 15. PMID 21247494 DOI: 10.1186/1471-2350-12-15 |
0.763 |
|
| 2010 |
Clark AG, Wang X, Matise T. Contrasting methods of quantifying fine structure of human recombination Annual Review of Genomics and Human Genetics. 11: 45-64. PMID 20690817 DOI: 10.1146/Annurev-Genom-082908-150031 |
0.503 |
|
| 2009 |
Buyske S, Yang G, Matise TC, Gordon D. When a case is not a case: effects of phenotype misclassification on power and sample size requirements for the transmission disequilibrium test with affected child trios. Human Heredity. 67: 287-92. PMID 19172087 DOI: 10.1159/000194981 |
0.359 |
|
| 2007 |
Matise TC, Chen F, Chen W, De La Vega FM, Hansen M, He C, Hyland FC, Kennedy GC, Kong X, Murray SS, Ziegle JS, Stewart WC, Buyske S. A second-generation combined linkage physical map of the human genome. Genome Research. 17: 1783-6. PMID 17989245 DOI: 10.1101/Gr.7156307 |
0.741 |
|
| 2006 |
Buyske S, Bates ME, Gharani N, Matise TC, Tischfield JA, Manowitz P. Cognitive traits link to human chromosomal regions. Behavior Genetics. 36: 65-76. PMID 16341908 DOI: 10.1007/S10519-005-9008-9 |
0.336 |
|
| 2005 |
Grahn RA, Lemesch BM, Millon LV, Matise T, Rogers QR, Morris JG, Fretwell N, Bailey SJ, Batt RM, Lyons LA. Localizing the X-linked orange colour phenotype using feline resource families. Animal Genetics. 36: 67-70. PMID 15670134 DOI: 10.1111/J.1365-2052.2005.01239.X |
0.366 |
|
| 2005 |
Kong X, Matise TC. MAP-O-MAT: internet-based linkage mapping Bioinformatics. 21: 557-559. PMID 15374870 DOI: 10.1093/Bioinformatics/Bti024 |
0.449 |
|
| 2004 |
Kong X, Murphy K, Raj T, He C, White PS, Matise TC. A combined linkage-physical map of the human genome. American Journal of Human Genetics. 75: 1143-8. PMID 15486828 DOI: 10.1086/426405 |
0.76 |
|
| 2003 |
Majewski J, Schultz DW, Weleber RG, Schain MB, Edwards AO, Matise TC, Acott TS, Ott J, Klein ML. Age-related macular degeneration--a genome scan in extended families. American Journal of Human Genetics. 73: 540-50. PMID 12900797 DOI: 10.1086/377701 |
0.38 |
|
| 2003 |
Clark AG, Nielsen R, Signorovitch J, Matise TC, Glanowski S, Heil J, Winn-Deen ES, Holden AL, Lai E. Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome. American Journal of Human Genetics. 73: 285-300. PMID 12844287 DOI: 10.1086/377138 |
0.456 |
|
| 2003 |
Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. American Journal of Human Genetics. 73: 271-84. PMID 12844283 DOI: 10.1086/377137 |
0.744 |
|
| 2002 |
DeWan AT, Parrado AR, Matise TC, Leal SM. Map error reduction: using genetic and sequence-based physical maps to order closely linked markers. Human Heredity. 54: 34-44. PMID 12446985 DOI: 10.1159/000066697 |
0.483 |
|
| 2002 |
Matise TC, Porter CJ, Buyske S, Cuttichia AJ, Sulman EP, White PS. Systematic evaluation of map quality: human chromosome 22. American Journal of Human Genetics. 70: 1398-410. PMID 11992248 DOI: 10.1086/340605 |
0.424 |
|
| 2002 |
Chowdhary BP, Raudsepp T, Honeycutt D, Owens EK, Piumi F, Guérin G, Matise TC, Kata SR, Womack JE, Skow LC. Construction of a 5000(rad) whole-genome radiation hybrid panel in the horse and generation of a comprehensive and comparative map for ECA11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 89-94. PMID 11889556 DOI: 10.1007/S00335-001-2089-8 |
0.445 |
|
| 2002 |
DeWan AT, Parrado AR, Matise TC, Leal SM. The map problem: a comparison of genetic and sequence-based physical maps. American Journal of Human Genetics. 70: 101-7. PMID 11706388 DOI: 10.1086/324774 |
0.491 |
|
| 2001 |
Puca AA, Daly MJ, Brewster SJ, Matise TC, Barrett J, Shea-Drinkwater M, Kang S, Joyce E, Nicoli J, Benson E, Kunkel LM, Perls T. A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4. Proceedings of the National Academy of Sciences of the United States of America. 98: 10505-8. PMID 11526246 DOI: 10.1073/Pnas.181337598 |
0.421 |
|
| 2001 |
White PS, Thompson PM, Seifried BA, Sulman EP, Jensen SJ, Guo C, Maris JM, Hogarty MD, Allen C, Biegel JA, Matise TC, Gregory SG, Reynolds CP, Brodeur GM. Detailed molecular analysis of 1p36 in neuroblastoma. Medical and Pediatric Oncology. 36: 37-41. PMID 11464901 DOI: 10.1002/1096-911X(20010101)36:1<37::Aid-Mpo1010>3.0.Co;2-L |
0.342 |
|
| 2001 |
White PS, Matise TC. Genomic mapping and mapping databases. Methods of Biochemical Analysis. 43: 111-153. PMID 11449722 DOI: 10.1002/0471223921.Ch6 |
0.451 |
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| 2000 |
Faraone SV, Meyer J, Matise T, Svrakic D, Pepple J, Malaspina D, Suarez B, Hampe C, Chan G, Aelony A, Friedman JH, Kaufmann C, Cloninger CR, Tsuang MT. Suggestive linkage of chromosome 10p to schizophrenia is not due to transmission ratio distortion. American Journal of Medical Genetics. 88: 607-8. PMID 10581477 DOI: 10.1002/(Sici)1096-8628(19991215)88:6<607::Aid-Ajmg6>3.0.Co;2-Q |
0.334 |
|
| 1999 |
White PS, Forus A, Matise TC, Schutte BC, Spieker N, Stanier P, Vance JM, Gregory SG. Report of the fifth international workshop on human chromosome 1 mapping 1999 Cytogenetics and Cell Genetics. 87: 143-171. PMID 10702659 DOI: 10.1159/000015458 |
0.37 |
|
| 1999 |
Marinov M, Matise TC, Lathrop GM, Weeks DE. A comparison of two algorithms, MultiMap and gene mapping system, for automated construction of genetic linkage maps. Genetic Epidemiology. 17: S649-54. PMID 10597508 DOI: 10.1002/Gepi.13701707106 |
0.408 |
|
| 1999 |
White PS, Sulman EP, Porter CJ, Matise TC. A comprehensive view of human chromosome 1. Genome Research. 9: 978-88. PMID 10523526 DOI: 10.1101/Gr.9.10.978 |
0.424 |
|
| 1999 |
Steen RG, Kwitek-Black AE, Glenn C, Gullings-Handley J, Etten WV, Atkinson OS, Appel D, Twigger S, Muir M, Mull T, Granados M, Kissebah M, Russo K, Crane R, Popp M, ... ... Matise T, et al. A high-density integrated genetic linkage and radiation hybrid map of the laboratory rat. Genome Research. 9. DOI: 10.1101/Gr.9.6.Ap1 |
0.497 |
|
| 1998 |
Deloukas P, Schuler GD, Gyapay G, Beasley EM, Soderlund C, Rodriguez-Tomé P, Hui L, Matise TC, McKusick KB, Beckmann JS, Bentolila S, Bihoreau M, Birren BB, Browne J, Butler A, et al. A physical map of 30,000 human genes. Science (New York, N.Y.). 282: 744-6. PMID 9784132 DOI: 10.1126/Science.282.5389.744 |
0.47 |
|
| 1998 |
Klein ML, Schultz DW, Edwards A, Matise TC, Rust K, Berselli CB, Trzupek K, Weleber RG, Ott J, Wirtz MK, Acott TS. Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q. Archives of Ophthalmology (Chicago, Ill. : 1960). 116: 1082-8. PMID 9715689 DOI: 10.1001/Archopht.116.8.1082 |
0.356 |
|
| 1998 |
Faraone SV, Matise T, Svrakic D, Pepple J, Malaspina D, Suarez B, Hampe C, Zambuto CT, Schmitt K, Meyer J, Markel P, Lee H, Harkavy Friedman J, Kaufmann C, Cloninger CR, et al. Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium. American Journal of Medical Genetics. 81: 290-5. PMID 9674973 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<290::Aid-Ajmg3>3.0.Co;2-Y |
0.346 |
|
| 1998 |
Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD, Meyer J, Zambuto CT, Schmitt K, Matise TC, Friedman JMH, Hampe C, Lee H, Shore D, Wynne D, et al. NIMH genetics initiative millennium Schizophrenia consortium: Linkage analysis of African-American pedigrees American Journal of Medical Genetics - Neuropsychiatric Genetics. 81: 282-289. PMID 9674972 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<282::Aid-Ajmg2>3.0.Co;2-W |
0.364 |
|
| 1998 |
Cloninger CR, Kaufmann CA, Faraone SV, Malaspina D, Svrakic DM, Harkavy-Friedman J, Suarez BK, Matise TC, Shore D, Lee H, Hampe CL, Wynne D, Drain C, Markel PD, Zambuto CT, et al. Genome-wide search for Schizophrenia susceptibility loci: The NIMH genetics initiative and millennium consortium American Journal of Medical Genetics - Neuropsychiatric Genetics. 81: 275-281. PMID 9674971 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<275::Aid-Ajmg1>3.0.Co;2-T |
0.386 |
|
| 1998 |
Brown DM, Matise TC, Koike G, Simon JS, Winer ES, Zangen S, McLaughlin MG, Shiozawa M, Atkinson OS, Hudson JR, Chakravarti A, Lander ES, Jacob HJ. An integrated genetic linkage map of the laboratory rat. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 521-30. PMID 9657848 DOI: 10.1007/S003359900812 |
0.472 |
|
| 1997 |
Jensen SJ, Sulman EP, Maris JM, Matise TC, Vojta PJ, Barrett JC, Brodeur GM, White PS. An integrated transcript map of human chromosome 1p35-p36. Genomics. 42: 126-36. PMID 9177782 DOI: 10.1006/Geno.1997.4714 |
0.503 |
|
| 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, ... ... Matise TC, 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 |
0.306 |
|
| 1996 |
Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, ... ... Matise TC, et al. A gene map of the human genome. Science (New York, N.Y.). 274: 540-6. PMID 8849440 DOI: 10.1126/Science.274.5287.540 |
0.487 |
|
| 1996 |
Weith A, Brodeur GM, Bruns GAP, Matise TC, Mischke D, Nizetic D, Seldin MF, Roy NV, Vance JM. Report of the second international workshop on human chromosome 1 mapping 1995. Cytogenetic and Genome Research. 72: 113-154. DOI: 10.1159/000134173 |
0.37 |
|
| 1995 |
Matise TC. Genome scanning for complex disease genes using the transmission/disequilibrium test and haplotype-based haplotype relative risk Genetic Epidemiology. 12: 641-645. PMID 8787987 DOI: 10.1002/Gepi.1370120620 |
0.437 |
|
| 1995 |
Kobayashi H, Baumbach L, Matise TC, Schiavi A, Greenberg F, Hoffman E. A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3–q11.2 Human Molecular Genetics. 4: 1213-1216. PMID 8528211 DOI: 10.1093/Hmg/4.7.1213 |
0.332 |
|
| 1995 |
Kobayashi H, Matise TC, Perlin MW, Marks HG, Hoffman EP. Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods. Human Genetics. 95: 483-90. PMID 7759066 DOI: 10.1007/Bf00223857 |
0.481 |
|
| 1995 |
Matise TC, Schroeder MD, Chiarulli DM, Weeks DE. Parallel computation of genetic likelihoods using CRI-MAP, PVM, and a network of distributed workstations Human Heredity. 45: 103-116. PMID 7750973 DOI: 10.1159/000154268 |
0.453 |
|
| 1995 |
Shaw SH, Farr JEW, Thiel BA, Matise TC, Weissenbach J, Chakaravarti A, Richard CW. A Radiation Hybrid Map of 95 STSs Spanning Human Chromosome 13q Genomics. 27: 502-510. PMID 7558033 DOI: 10.1006/Geno.1995.1083 |
0.428 |
|
| 1994 |
Attwood J, Chiano M, Collins A, Donis-Keller H, Dracopoli N, Fountain J, Falk C, Goudie D, Gusella J, Haines J, Armour JAL, Jeffreys AJ, Kwiatkowski D, Lathrop M, Matise T, et al. CEPH Consortium Map of Chromosome 9 Genomics. 19: 203-214. PMID 8188250 DOI: 10.1006/Geno.1994.1049 |
0.455 |
|
| 1994 |
Matise TC, Perlin M, Chakravarti A. Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. Nature Genetics. 6: 384-90. PMID 8054979 DOI: 10.1038/Ng0494-384 |
0.496 |
|
| 1994 |
Puffenberger EG, Kauffman ER, Bolk S, Matise TC, Washington SS, Angrist M, Weissenbach J, Garver KL, Mascari M, Ladda R. Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. Human Molecular Genetics. 3: 1217-25. PMID 7987295 DOI: 10.1093/Hmg/3.8.1217 |
0.441 |
|
| 1994 |
Finegold DN, Armitage MM, Galiani M, Matise TC, Pandian MR, Perry YM, Deka R, Ferrell RE. Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13. Pediatric Research. 36: 414-7. PMID 7808841 DOI: 10.1203/00006450-199409000-00024 |
0.354 |
|
| 1994 |
Dracopoli NC, Bruns GAP, Brodeur GM, Landes GM, Matise TC, Seldin MF, Vance JM, Weith A. Report of the first international workshop on human chomosome 1 mapping 1994 Cytogenetic and Genome Research. 67: 143-174. DOI: 10.1159/000133816 |
0.369 |
|
| 1994 |
Matise TC, Perlin M, Chakravarti A. Erratum: Corrigendum: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map Nature Genetics. 7: 215-215. DOI: 10.1038/Ng0694-215B |
0.501 |
|
| 1993 |
Angrist M, Kauffman E, Slaugenhaupt SA, Matise TC, Puffenberger EG, Washington SS, Lipson A, Cass DT, Reyna T, Weeks DE. A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. Nature Genetics. 4: 351-6. PMID 8401581 DOI: 10.1038/Ng0893-351 |
0.331 |
|
| 1993 |
McInnis MG, Chakravarti A, Blaschak J, Petersen MB, Sharma V, Avramopoulos D, Blouin JL, König U, Brahe C, Matise TC. A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM. Genomics. 16: 562-71. PMID 8325627 DOI: 10.1006/Geno.1993.1231 |
0.466 |
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