| Year |
Citation |
Score |
| 2019 |
Panigrahi S, Zhu J, Sabatti C. Selection-adjusted inference: an application to confidence intervals for cis-eQTL effect sizes. Biostatistics (Oxford, England). PMID 31301173 DOI: 10.1093/biostatistics/kxz024 |
0.4 |
|
| 2019 |
Zhu J, Zhao Q, Katsevich E, Sabatti C. Exploratory Gene Ontology Analysis with Interactive Visualization. Scientific Reports. 9: 7793. PMID 31127124 DOI: 10.1038/s41598-019-42178-x |
0.4 |
|
| 2018 |
Neal JT, Li X, Zhu J, Giangarra V, Grzeskowiak CL, Ju J, Liu IH, Chiou SH, Salahudeen AA, Smith AR, Deutsch BC, Liao L, Zemek AJ, Zhao F, Karlsson K, ... ... Sabatti C, et al. Organoid Modeling of the Tumor Immune Microenvironment. Cell. 175: 1972-1988.e16. PMID 30550791 DOI: 10.1016/j.cell.2018.11.021 |
0.4 |
|
| 2018 |
Mooney JA, Huber CD, Service S, Sul JH, Marsden CD, Zhang Z, Sabatti C, Ruiz-Linares A, Bedoya G, Freimer N, Lohmueller KE. Understanding the Hidden Complexity of Latin American Population Isolates. American Journal of Human Genetics. 103: 707-726. PMID 30401458 DOI: 10.1016/j.ajhg.2018.09.013 |
0.48 |
|
| 2018 |
Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, ... ... Sabatti C, et al. Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. PMID 29549319 DOI: 10.1038/s41593-018-0102-8 |
0.36 |
|
| 2017 |
Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, ... ... Sabatti C, et al. Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nature Neuroscience. 20: 1661-1668. PMID 29184211 DOI: 10.1038/s41593-017-0017-9 |
0.36 |
|
| 2016 |
Peterson CB, Service SK, Jasinska AJ, Gao F, Zelaya I, Teshiba TM, Bearden CE, Cantor RM, Reus VI, Macaya G, López-Jaramillo C, Bogomolov M, Benjamini Y, Eskin E, Coppola G, ... ... Sabatti C, et al. Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder. Plos Genetics. 12: e1006046. PMID 27176483 DOI: 10.1371/journal.pgen.1006046 |
0.48 |
|
| 2015 |
Pagani L, St Clair PA, Teshiba TM, Service SK, Fears SC, Araya C, Araya X, Bejarano J, Ramirez M, Castrillón G, Gomez-Makhinson J, Lopez MC, Montoya G, Montoya CP, Aldana I, ... ... Sabatti C, et al. Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder. Proceedings of the National Academy of Sciences of the United States of America. PMID 26712028 DOI: 10.1073/pnas.1513525113 |
0.48 |
|
| 2015 |
Bogdan M, van den Berg E, Sabatti C, Su W, Candès EJ. SLOPE-ADAPTIVE VARIABLE SELECTION VIA CONVEX OPTIMIZATION. The Annals of Applied Statistics. 9: 1103-1140. PMID 26709357 DOI: 10.1214/15-AOAS842 |
0.48 |
|
| 2015 |
Peterson CB, Bogomolov M, Benjamini Y, Sabatti C. Many Phenotypes Without Many False Discoveries: Error Controlling Strategies for Multitrait Association Studies. Genetic Epidemiology. PMID 26626037 DOI: 10.1002/gepi.21942 |
0.48 |
|
| 2015 |
Banda Y, Kvale MN, Hoffmann TJ, Hesselson SE, Ranatunga D, Tang H, Sabatti C, Croen LA, Dispensa BP, Henderson M, Iribarren C, Jorgenson E, Kushi LH, Ludwig D, Olberg D, et al. Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics. PMID 26092716 DOI: 10.1534/genetics.115.178616 |
0.48 |
|
| 2015 |
Fears SC, Schür R, Sjouwerman R, Service SK, Araya C, Araya X, Bejarano J, Knowles E, Gomez-Makhinson J, Lopez MC, Aldana I, Teshiba TM, Abaryan Z, Al-Sharif NB, Navarro L, ... ... Sabatti C, et al. Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder. Brain : a Journal of Neurology. 138: 2087-102. PMID 25943422 DOI: 10.1093/brain/awv106 |
0.48 |
|
| 2014 |
Fears SC, Service SK, Kremeyer B, Araya C, Araya X, Bejarano J, Ramirez M, Castrillón G, Gomez-Franco J, Lopez MC, Montoya G, Montoya P, Aldana I, Teshiba TM, Abaryan Z, ... ... Sabatti C, et al. Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. Jama Psychiatry. 71: 375-87. PMID 24522887 DOI: 10.1001/jamapsychiatry.2013.4100 |
0.48 |
|
| 2014 |
Service SK, Teslovich TM, Fuchsberger C, Ramensky V, Yajnik P, Koboldt DC, Larson DE, Zhang Q, Lin L, Welch R, Ding L, McLellan MD, O'Laughlin M, Fronick C, Fulton LL, ... ... Sabatti C, et al. Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. Plos Genetics. 10: e1004147. PMID 24497850 DOI: 10.1371/journal.pgen.1004147 |
0.48 |
|
| 2013 |
Buizer-Voskamp JE, Blauw HM, Boks MP, van Eijk KR, Veldink JH, Hennekam EA, Vorstman JA, Mulder F, Tiemeier H, Uitterlinden AG, Kiemeney LA, van den Berg LH, Kahn RS, Sabatti C, Ophoff RA. Increased paternal age and the influence on burden of genomic copy number variation in the general population. Human Genetics. 132: 443-50. PMID 23315237 DOI: 10.1007/s00439-012-1261-4 |
0.48 |
|
| 2012 |
Zhang Z, Lange K, Sabatti C. Reconstructing DNA copy number by joint segmentation of multiple sequences. Bmc Bioinformatics. 13: 205. PMID 22897923 DOI: 10.1186/1471-2105-13-205 |
0.48 |
|
| 2012 |
Service SK, Verweij KJ, Lahti J, Congdon E, Ekelund J, Hintsanen M, Räikkönen K, Lehtimäki T, Kähönen M, Widen E, Taanila A, Veijola J, Heath AC, Madden PA, Montgomery GW, ... Sabatti C, et al. A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales. Translational Psychiatry. 2: e116. PMID 22832960 DOI: 10.1038/tp.2012.37 |
0.48 |
|
| 2011 |
Visnyei K, Onodera H, Damoiseaux R, Saigusa K, Petrosyan S, De Vries D, Ferrari D, Saxe J, Panosyan EH, Masterman-Smith M, Mottahedeh J, Bradley KA, Huang J, Sabatti C, Nakano I, et al. A molecular screening approach to identify and characterize inhibitors of glioblastoma stem cells. Molecular Cancer Therapeutics. 10: 1818-28. PMID 21859839 DOI: 10.1158/1535-7163.MCT-11-0268 |
0.48 |
|
| 2011 |
Pietiläinen OPH, Rehnström K, Jakkula E, Service SK, Congdon E, Tilgmann C, Hartikainen AL, Taanila A, Heikura U, Paunio T, Ripatti S, Jarvelin MR, Isohanni M, Sabatti C, Palotie A, et al. Phenotype mining in CNV carriers from a population cohort Human Molecular Genetics. 20: 2686-2695. PMID 21505072 DOI: 10.1093/hmg/ddr162 |
0.48 |
|
| 2011 |
Buizer-Voskamp JE, Muntjewerff JW, Strengman E, Sabatti C, Stefansson H, Vorstman JA, Ophoff RA. Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients. Biological Psychiatry. 70: 655-62. PMID 21489405 DOI: 10.1016/j.biopsych.2011.02.015 |
0.48 |
|
| 2011 |
Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM. Family-based genetic association study of DLGAP3 in Tourette Syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 108-14. PMID 21184590 DOI: 10.1002/ajmg.b.31134 |
0.48 |
|
| 2010 |
James GM, Sabatti C, Zhou N, Zhu J. Sparse Regulatory Networks. The Annals of Applied Statistics. 4: 663-686. PMID 21625366 DOI: 10.1214/10-AOAS350 |
0.48 |
|
| 2010 |
Zhang Z, Lange K, Ophoff R, Sabatti C. RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. The Annals of Applied Statistics. 4: 1749-1773. PMID 21572975 DOI: 10.1214/10-AOAS357 |
0.48 |
|
| 2010 |
Kang HM, Sul JH, Service SK, Zaitlen NA, Kong SY, Freimer NB, Sabatti C, Eskin E. Variance component model to account for sample structure in genome-wide association studies. Nature Genetics. 42: 348-54. PMID 20208533 DOI: 10.1038/ng.548 |
0.48 |
|
| 2010 |
Knight S, Coon H, Johnson M, Leppert MF, Camp NJ, McMahon WM, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Santangelo S, Stewart SE, Scharf J, ... ... Sabatti C, et al. Linkage analysis of Tourette syndrome in a large Utah pedigree American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 656-662. PMID 19777563 DOI: 10.1002/ajmg.b.31035 |
0.48 |
|
| 2010 |
Ghiani CA, Starcevic M, Rodriguez-Fernandez IA, Nazarian R, Cheli VT, Chan LN, Malvar JS, de Vellis J, Sabatti C, Dell'Angelica EC. The dysbindin-containing complex (BLOC-1) in brain: developmental regulation, interaction with SNARE proteins and role in neurite outgrowth. Molecular Psychiatry. 15: 115, 204-15. PMID 19546860 DOI: 10.1038/mp.2009.58 |
0.48 |
|
| 2009 |
Hattori D, Chen Y, Matthews BJ, Salwinski L, Sabatti C, Grueber WB, Zipursky SL. Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoforms. Nature. 461: 644-8. PMID 19794492 DOI: 10.1038/nature08431 |
0.48 |
|
| 2009 |
Wang H, Veldink JH, Blauw H, van den Berg LH, Ophoff RA, Sabatti C. Markov Models for inferring copy number variations from genotype data on Illumina platforms. Human Heredity. 68: 1-22. PMID 19339782 DOI: 10.1159/000210445 |
0.48 |
|
| 2009 |
Jasinska AJ, Service S, Jawaheer D, DeYoung J, Levinson M, Zhang Z, Kremeyer B, Muller H, Aldana I, Garcia J, Restrepo G, Lopez C, Palacio C, Duque C, Parra M, ... ... Sabatti C, et al. A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 998-1006. PMID 19319892 DOI: 10.1002/ajmg.b.30956 |
0.48 |
|
| 2009 |
Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, ... ... Sabatti C, et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics. 41: 47-55. PMID 19060911 DOI: 10.1038/ng.269 |
0.48 |
|
| 2009 |
Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, et al. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nature Genetics. 41: 35-46. PMID 19060910 DOI: 10.1038/ng.271 |
0.48 |
|
| 2009 |
Rujescu D, Ingason A, Cichon S, Pietiläinen OP, Barnes MR, Toulopoulou T, Picchioni M, Vassos E, Ettinger U, Bramon E, Murray R, Ruggeri M, Tosato S, Bonetto C, Steinberg S, ... ... Sabatti C, et al. Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics. 18: 988-96. PMID 18945720 DOI: 10.1093/hmg/ddn351 |
0.48 |
|
| 2008 |
Sabatti C, Lange K. Bayesian Gaussian Mixture Models for High-Density Genotyping Arrays. Journal of the American Statistical Association. 103: 89-100. PMID 21572926 DOI: 10.1198/016214507000000338. |
0.48 |
|
| 2008 |
Vrijenhoek T, Buizer-Voskamp JE, van der Stelt I, Strengman E, Sabatti C, Geurts van Kessel A, Brunner HG, Ophoff RA, Veltman JA. Recurrent CNVs disrupt three candidate genes in schizophrenia patients. American Journal of Human Genetics. 83: 504-10. PMID 18940311 DOI: 10.1016/j.ajhg.2008.09.011 |
0.48 |
|
| 2008 |
Stefansson H, Rujescu D, Cichon S, Pietiläinen OP, Ingason A, Steinberg S, Fossdal R, Sigurdsson E, Sigmundsson T, Buizer-Voskamp JE, Hansen T, Jakobsen KD, Muglia P, Francks C, Matthews PM, ... ... Sabatti C, et al. Large recurrent microdeletions associated with schizophrenia. Nature. 455: 232-6. PMID 18668039 DOI: 10.1038/nature07229 |
0.48 |
|
| 2008 |
Cha YH, Brodsky J, Ishiyama G, Sabatti C, Baloh RW. Clinical features and associated syndromes of mal de debarquement. Journal of Neurology. 255: 1038-44. PMID 18500497 DOI: 10.1007/s00415-008-0837-3 |
0.48 |
|
| 2008 |
Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. Neurology. 70: 1495-6. PMID 18413575 DOI: 10.1212/01.wnl.0000296833.25484.bb |
0.48 |
|
| 2008 |
Service S, Molina J, DeYoung J, Jawaheer D, Aldana I, Vu T, Araya C, Araya X, Bejarano J, Fournier E, Ramirez M, Mathews CA, Davanzo P, Macaya G, Sandkuijl L, ... Sabatti C, et al. Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder (American Journal of Medical Genetics, Part B: Neuropsychiatrics Genetics) American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147: 540. DOI: 10.1002/ajmg.b.30438 |
0.48 |
|
| 2007 |
Sabatti C. Avoiding false discoveries in association studies. Methods in Molecular Biology (Clifton, N.J.). 376: 195-211. PMID 17984547 DOI: 10.1007/978-1-59745-389-9_14 |
0.48 |
|
| 2007 |
Cha YH, Brodsky J, Ishiyama G, Sabatti C, Baloh RW. The relevance of migraine in patients with Ménière's disease Acta Oto-Laryngologica. 127: 1241-1245. PMID 17851970 DOI: 10.1080/00016480701242469 |
0.48 |
|
| 2007 |
Ayers KL, Sabatti C, Lange K. A dictionary model for haplotyping, genotype calling, and association testing. Genetic Epidemiology. 31: 672-83. PMID 17487885 DOI: 10.1002/gepi.20232 |
0.48 |
|
| 2007 |
Service S, Sabatti C, Freimer N, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, Van Duijn C, et al. Tag SNPs chosen from HapMap perform well in several population isolates Genetic Epidemiology. 31: 189-194. PMID 17323370 DOI: 10.1002/gepi.20201 |
0.48 |
|
| 2007 |
Pauls D, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Scharf JM, Santangelo S, Stewart SE, Platko J, Pauls DL, Cox NJ, Robertson MM, Service S, ... ... Sabatti C, et al. Genome scan for tourette disorder in affected-sibling-pair and multigenerational families American Journal of Human Genetics. 80: 265-272. PMID 17304708 DOI: 10.1086/511052 |
0.48 |
|
| 2007 |
Freimer NB, Sabatti C. Human genetics: variants in common diseases. Nature. 445: 828-30. PMID 17293879 DOI: 10.1038/nature05568 |
0.48 |
|
| 2006 |
Chen Y, Lin CH, Sabatti C. Volume measures for linkage disequilibrium. Bmc Genetics. 7: 54. PMID 17112381 DOI: 10.1186/1471-2156-7-54 |
0.48 |
|
| 2006 |
Wang H, Lin CH, Service S, Chen Y, Freimer N, Sabatti C. Linkage disequilibrium and haplotype homozygosity in population samples genotyped at a high marker density. Human Heredity. 62: 175-89. PMID 17077642 DOI: 10.1159/000096599 |
0.48 |
|
| 2006 |
Keen-Kim D, Mathews CA, Reus VI, Lowe TL, Herrera LD, Budman CL, Gross-Tsur V, Pulver AE, Bruun RD, Erenberg G, Naarden A, Sabatti C, Freimer NB. Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Human Molecular Genetics. 15: 3324-8. PMID 17035247 DOI: 10.1093/hmg/ddl408 |
0.48 |
|
| 2006 |
Herzberg I, Jasinska A, GarcÃa J, Jawaheer D, Service S, Kremeyer B, Duque C, Parra MV, Vega J, Ortiz D, Carvajal L, Polanco G, Restrepo GJ, López C, Palacio C, ... ... Sabatti C, et al. Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34. Human Molecular Genetics. 15: 3146-53. PMID 16984960 DOI: 10.1093/hmg/ddl254 |
0.48 |
|
| 2006 |
Ayers KL, Sabatti C, Lange K. Reconstructing ancestral haplotypes with a dictionary model. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 13: 767-85. PMID 16706724 DOI: 10.1089/cmb.2006.13.767 |
0.48 |
|
| 2006 |
Service S, Molina J, Deyoung J, Jawaheer D, Aldana I, Vu T, Araya C, Araya X, Bejarano J, Fournier E, Ramirez M, Mathews CA, Davanzo P, Macaya G, Sandkuijl L, ... Sabatti C, et al. Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 367-73. PMID 16652356 DOI: 10.1002/ajmg.b.30323 |
0.48 |
|
| 2006 |
Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, ... ... Sabatti C, et al. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nature Genetics. 38: 556-60. PMID 16582909 DOI: 10.1038/ng1770 |
0.48 |
|
| 2006 |
Sabatti C, James GM. Bayesian sparse hidden components analysis for transcription regulation networks. Bioinformatics (Oxford, England). 22: 739-46. PMID 16368767 DOI: 10.1093/bioinformatics/btk017 |
0.48 |
|
| 2006 |
Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Human Molecular Genetics. 15: 251-8. PMID 16330481 DOI: 10.1093/hmg/ddi441 |
0.48 |
|
| 2006 |
Sabatti C, Satten GA, Allen AS, Epstein MP, Chatterjee N, Spinka C, Chen J, Carroll RJ, Tzeng JY, Roeder K, Li H, Lin DY, Zeng D. Journal of the American Statistical Association: Comment Journal of the American Statistical Association. 101: 104-118. DOI: 10.1198/016214505000000817 |
0.48 |
|
| 2006 |
Sabatti C, Lange K. Genomewide Motif Identification Using a Dictionary Model Genomics and Proteomics Engineering in Medicine and Biology. 157-172. DOI: 10.1002/9780470052198.ch6 |
0.48 |
|
| 2005 |
Boscolo R, Sabatti C, Liao JC, Roychowdhury VP. A generalized framework for network component analysis. Ieee/Acm Transactions On Computational Biology and Bioinformatics / Ieee, Acm. 2: 289-301. PMID 17044167 DOI: 10.1109/TCBB.2005.47 |
0.48 |
|
| 2005 |
Erickson S, Sabatti C. Empirical bayes estimation of a sparse vector of gene expression changes. Statistical Applications in Genetics and Molecular Biology. 4: Article22. PMID 16646840 DOI: 10.2202/1544-6115.1132 |
1 |
|
| 2005 |
Falcón-Pérez JM, Nazarian R, Sabatti C, Dell'Angelica EC. Distribution and dynamics of Lamp1-containing endocytic organelles in fibroblasts deficient in BLOC-3. Journal of Cell Science. 118: 5243-55. PMID 16249233 DOI: 10.1242/jcs.02633 |
0.48 |
|
| 2005 |
Riley R, Lee C, Sabatti C, Eisenberg D. Inferring protein domain interactions from databases of interacting proteins. Genome Biology. 6: R89. PMID 16207360 DOI: 10.1186/gb-2005-6-10-r89 |
0.48 |
|
| 2005 |
Freimer NB, Sabatti C. Guidelines for association studies in Human Molecular Genetics. Human Molecular Genetics. 14: 2481-3. PMID 16037069 DOI: 10.1093/hmg/ddi251 |
0.48 |
|
| 2005 |
Sabatti C, Rohlin L, Lange K, Liao JC. Vocabulon: a dictionary model approach for reconstruction and localization of transcription factor binding sites. Bioinformatics (Oxford, England). 21: 922-31. PMID 15509602 DOI: 10.1093/bioinformatics/bti083 |
0.48 |
|
| 2005 |
Fan J, Peng H, Huang T, Sabatti C, Craig BA, Huang J, Zhang CH, Zhang H, Kosorok MR, Shuangge M, Tibshirani R, Ren Y. Semilinear high-dimensional model for normalization of microarray data: A theoretical analysis and partial consistency Journal of the American Statistical Association. 100: 781-813. DOI: 10.1198/016214504000001781 |
0.48 |
|
| 2004 |
Sabatti C, Rohlin L. A Bayesian approach to expression network component analysis. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 4: 2933-6. PMID 17270892 DOI: 10.1109/IEMBS.2004.1403833 |
0.48 |
|
| 2004 |
Jen JC, Wang H, Lee H, Sabatti C, Trent R, Hannigan I, Brantberg K, Halmagyi GM, Nelson SF, Baloh RW. Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy Neurology. 63: 2376-2379. PMID 15623703 |
0.48 |
|
| 2004 |
Lee H, Wang H, Jen JC, Sabatti C, Baloh RW, Nelson SF. A novel mutation in KCNA1 causes episodic ataxia without myokymia. Human Mutation. 24: 536. PMID 15532032 DOI: 10.1002/humu.9295 |
0.48 |
|
| 2004 |
Freimer N, Sabatti C. The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology. Nature Genetics. 36: 1045-51. PMID 15454942 DOI: 10.1038/ng1433 |
0.48 |
|
| 2004 |
Kao KC, Yang YL, Boscolo R, Sabatti C, Roychowdhury V, Liao JC. Transcriptome-based determination of multiple transcription regulator activities in Escherichia coli by using network component analysis. Proceedings of the National Academy of Sciences of the United States of America. 101: 641-6. PMID 14694202 DOI: 10.1073/pnas.0305287101 |
0.48 |
|
| 2004 |
Sabatti C. Interplay in the computational analysis of genomic regulatory sequences and microarray expression data Current Genomics. 5: 439-442. DOI: 10.2174/1389202043349084 |
0.48 |
|
| 2003 |
Liao JC, Boscolo R, Yang YL, Tran LM, Sabatti C, Roychowdhury VP. Network component analysis: reconstruction of regulatory signals in biological systems. Proceedings of the National Academy of Sciences of the United States of America. 100: 15522-7. PMID 14673099 DOI: 10.1073/pnas.2136632100 |
0.48 |
|
| 2003 |
Yang RC, Sabatti C, Risch N. Gametic and zygotic associations [2] (multiple letters) Genetics. 165: 447-452. PMID 14575045 |
0.48 |
|
| 2003 |
Karsten SL, Kudo LC, Jackson R, Sabatti C, Kornblum HI, Geschwind DH. Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks. Developmental Biology. 261: 165-82. PMID 12941627 DOI: 10.1016/S0012-1606(03)00274-4 |
0.48 |
|
| 2003 |
Sabatti C, Service S, Freimer N. False discovery rate in linkage and association genome screens for complex disorders. Genetics. 164: 829-33. PMID 12807801 |
0.48 |
|
| 2003 |
Freimer N, Sabatti C. The human phenome project. Nature Genetics. 34: 15-21. PMID 12721547 DOI: 10.1038/ng0503-15 |
0.48 |
|
| 2003 |
Sabatti C, Rohlin L, Liao J. Dictionary model for the analysis of E. Coli promoter regions Annual International Conference of the Ieee Engineering in Medicine and Biology - Proceedings. 4: 3711-3714. |
0.48 |
|
| 2002 |
Jen J, Coulin CJ, Bosley TM, Salih MAM, Sabatti C, Nelson SF, Baloh RW. Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25 Neurology. 59: 432-435. PMID 12177379 |
0.48 |
|
| 2002 |
Sabatti C, Rohlin L, Oh MK, Liao JC. Co-expression pattern from DNA microarray experiments as a tool for operon prediction. Nucleic Acids Research. 30: 2886-93. PMID 12087173 |
0.48 |
|
| 2002 |
Sabatti C, Risch N. Homozygosity and linkage disequilibrium. Genetics. 160: 1707-19. PMID 11973323 |
0.48 |
|
| 2002 |
Sabatti C, Karsten SL, Geschwind DH. Thresholding rules for recovering a sparse signal from microarray experiments. Mathematical Biosciences. 176: 17-34. PMID 11867081 DOI: 10.1016/S0025-5564(01)00102-X |
0.48 |
|
| 2002 |
Karsten SL, Van Deerlin VM, Sabatti C, Gill LH, Geschwind DH. An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis. Nucleic Acids Research. 30: E4. PMID 11788730 |
0.48 |
|
| 2002 |
Sabatti C. Statistical issues in microarray analysis Current Genomics. 3: 7-12. DOI: 10.2174/1389202023350679 |
0.48 |
|
| 2002 |
Sabatti C. Measuring dependency with volume tests American Statistician. 56: 191-195. DOI: 10.1198/000313002128 |
0.48 |
|
| 2001 |
Pastinen T, Perola M, Ignatius J, Sabatti C, Tainola P, Levander M, Syvänen AC, Peltonen L. Dissecting a population genome for targeted screening of disease mutations Human Molecular Genetics. 10: 2961-2972. PMID 11751678 |
0.48 |
|
| 2001 |
Liu JS, Sabatti C, Teng J, Keats BJB, Risch N. Bayesian analysis of haplotypes for linkage disequilibrium mapping Genome Research. 11: 1716-1724. PMID 11591648 DOI: 10.1101/gr.194801 |
0.48 |
|
| 2000 |
Bressman SB, Sabatti C, Raymond D, de Leon D, Klein C, Kramer PL, Brin MF, Fahn S, Breakefield X, Ozelius LJ, Risch NJ. The DYT1 phenotype and guidelines for diagnostic testing. Neurology. 54: 1746-52. PMID 10802779 |
0.48 |
|
| 2000 |
Liu JS, Sabatti C. Generalised Gibbs sampler and multigrid Monte Carlo for Bayesian computation Biometrika. 87: 353-369. |
0.48 |
|
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