| Year |
Citation |
Score |
| 2024 |
He Z, Chu B, Yang J, Gu J, Chen Z, Liu L, Morrison T, Belloy ME, Qi X, Hejazi N, Mathur M, Le Guen Y, Tang H, Hastie T, Ionita-Laza I, ... Sabatti C, et al. In silico identification of putative causal genetic variants. Biorxiv : the Preprint Server For Biology. PMID 38464202 DOI: 10.1101/2024.02.28.582621 |
0.306 |
|
| 2021 |
Sesia M, Bates S, Candès E, Marchini J, Sabatti C. False discovery rate control in genome-wide association studies with population structure. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34580220 DOI: 10.1073/pnas.2105841118 |
0.307 |
|
| 2020 |
Bates S, Sesia M, Sabatti C, Candès E. Causal inference in genetic trio studies. Proceedings of the National Academy of Sciences of the United States of America. PMID 32948695 DOI: 10.1073/Pnas.2007743117 |
0.363 |
|
| 2020 |
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, Al-Sharif NB, ... ... Sabatti C, et al. Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder. Molecular Psychiatry. PMID 32606377 DOI: 10.1038/S41380-020-0805-6 |
0.355 |
|
| 2020 |
Sesia M, Katsevich E, Bates S, Candès E, Sabatti C. Publisher Correction: Multi-resolution localization of causal variants across the genome. Nature Communications. 11: 1799. PMID 32265451 DOI: 10.1038/S41467-020-15690-2 |
0.305 |
|
| 2020 |
Sesia M, Katsevich E, Bates S, Candès E, Sabatti C. Multi-resolution localization of causal variants across the genome. Nature Communications. 11: 1093. PMID 32107378 DOI: 10.1038/S41467-020-14791-2 |
0.405 |
|
| 2020 |
Sul JH, Service SK, Huang AY, Ramensky V, Hwang SG, Teshiba TM, Park Y, Ori APS, Zhang Z, Mullins N, Olde Loohuis LM, Fears SC, Araya C, Araya X, Spesny M, ... ... Sabatti C, et al. Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates. Translational Psychiatry. 10: 74. PMID 32094344 DOI: 10.1038/S41398-020-0758-1 |
0.578 |
|
| 2019 |
Katsevich E, Sabatti C. MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS. The Annals of Applied Statistics. 13: 1-33. PMID 31687060 DOI: 10.1214/18-Aoas1185 |
0.333 |
|
| 2019 |
Locke AE, Steinberg KM, Chiang CWK, Service SK, Havulinna AS, Stell L, Pirinen M, Abel HJ, Chiang CC, Fulton RS, Jackson AU, Kang CJ, Kanchi KL, Koboldt DC, Larson DE, ... ... Sabatti C, et al. Exome sequencing of Finnish isolates enhances rare-variant association power. Nature. PMID 31367044 DOI: 10.1038/S41586-019-1457-Z |
0.376 |
|
| 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 |
0.389 |
|
| 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, ... ... Sabatti C, et al. Genetic analyses of diverse populations improves discovery for complex traits. Nature. PMID 31217584 DOI: 10.1038/S41586-019-1310-4 |
0.379 |
|
| 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 |
0.337 |
|
| 2019 |
Loohuis LO, Jensen S, Teshiba T, Umanes MM, Vargas C, Escobar J, Reus V, Sabatti C, Bearden C, Lopez-Jaramillo C, Freimer N. The Relationship Between Genome-Wide Significant Gwas Loci And Psychiatric Phenotypes In A Colombian Population Isolate European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.079 |
0.373 |
|
| 2018 |
Sesia M, Sabatti C, Candès EJ. Gene hunting with hidden Markov model knockoffs. Biometrika. 106: 1-18. PMID 30799875 DOI: 10.1093/Biomet/Asy033 |
0.335 |
|
| 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 |
0.534 |
|
| 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 |
0.335 |
|
| 2017 |
Jasinska AJ, Zelaya I, Service SK, Peterson CB, Cantor RM, Choi OW, DeYoung J, Eskin E, Fairbanks LA, Fears S, Furterer AE, Huang YS, Ramensky V, Schmitt CA, Svardal H, ... ... Sabatti C, et al. Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate. Nature Genetics. PMID 29083405 DOI: 10.1038/Ng.3959 |
0.38 |
|
| 2016 |
Brzyski D, Peterson C, Sobczyk P, Candes E, Bogdan M, Sabatti C. Controlling the Rate of GWAS False Discoveries. Genetics. PMID 27784720 DOI: 10.1534/Genetics.116.193987 |
0.389 |
|
| 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 |
0.437 |
|
| 2016 |
Stell L, Sabatti C. Genetic Variant Selection: Learning Across Traits and Sites. Genetics. 202: 439-55. PMID 26680660 DOI: 10.1534/Genetics.115.184572 |
0.348 |
|
| 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 |
0.354 |
|
| 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 |
0.382 |
|
| 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 |
0.325 |
|
| 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 |
0.301 |
|
| 2015 |
Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Sabatti C, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306 |
0.339 |
|
| 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 |
0.39 |
|
| 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 |
0.42 |
|
| 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 |
0.352 |
|
| 2013 |
Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Sabatti C, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69 |
0.409 |
|
| 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 |
0.562 |
|
| 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 |
0.404 |
|
| 2012 |
Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... ... Sabatti C, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
0.307 |
|
| 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 |
0.417 |
|
| 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 |
0.33 |
|
| 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 |
0.52 |
|
| 2010 |
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, ... ... Sabatti C, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 466: 707-13. PMID 20686565 DOI: 10.1038/Nature09270 |
0.323 |
|
| 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 |
0.396 |
|
| 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 |
0.359 |
|
| 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 |
0.54 |
|
| 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 |
0.303 |
|
| 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 |
0.352 |
|
| 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 |
0.311 |
|
| 2009 |
Sabatti C, Lalanne C. Applied Statistical Genetics with R for Population-Based Association Studies Journal of Statistical Software. 31: 1-5. DOI: 10.18637/Jss.V031.B02 |
0.321 |
|
| 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 |
0.348 |
|
| 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 |
0.352 |
|
| 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 |
0.351 |
|
| 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 |
0.328 |
|
| 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 |
0.35 |
|
| 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 |
0.339 |
|
| 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 |
0.347 |
|
| 2007 |
Freimer NB, Sabatti C. Human genetics: variants in common diseases. Nature. 445: 828-30. PMID 17293879 DOI: 10.1038/Nature05568 |
0.33 |
|
| 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 |
0.38 |
|
| 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 |
0.379 |
|
| 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 |
0.395 |
|
| 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 |
0.304 |
|
| 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 |
0.389 |
|
| 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 |
0.379 |
|
| 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 |
0.378 |
|
| 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 |
0.306 |
|
| 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 |
0.519 |
|
| 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 |
0.305 |
|
| 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 DOI: 10.1212/01.Wnl.0000149498.79541.49 |
0.329 |
|
| 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 |
0.391 |
|
| 2003 |
Freimer N, Sabatti C. The human phenome project. Nature Genetics. 34: 15-21. PMID 12721547 DOI: 10.1038/Ng0503-15 |
0.335 |
|
| 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 DOI: 10.1093/Nar/Gkf388 |
0.305 |
|
| 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 DOI: 10.1093/Hmg/10.26.2961 |
0.328 |
|
| 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 |
0.32 |
|
| 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 DOI: 10.1212/Wnl.54.9.1746 |
0.314 |
|
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