| Year |
Citation |
Score |
| 2023 |
Siecinski SK, Giamberardino SN, Spanos M, Hauser AC, Gibson JR, Chandrasekhar T, Trelles MDP, Rockhill CM, Palumbo ML, Cundiff AW, Montgomery A, Siper P, Minjarez M, Nowinski LA, Marler S, ... ... Gregory SG, et al. Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder. Autism Research : Official Journal of the International Society For Autism Research. PMID 36609850 DOI: 10.1002/aur.2884 |
0.323 |
|
| 2019 |
Kousa YA, Zhu H, Fakhouri WD, Lei Y, Kinoshita A, Roushangar RR, Patel NK, Agopian AJ, Yang W, Leslie EJ, Busch TD, Mansour TA, Li X, Smith AL, Li EB, ... ... Gregory S, et al. The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation. Human Molecular Genetics. PMID 30689861 DOI: 10.1093/Hmg/Ddz010 |
0.415 |
|
| 2018 |
Towers AJ, Tremblay MW, Chung L, Li XL, Bey AL, Zhang W, Cao X, Wang X, Wang P, Duffney LJ, Siecinski SK, Xu S, Kim Y, Kong X, Gregory S, et al. Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders. Jci Insight. 3. PMID 30518695 DOI: 10.1172/Jci.Insight.120592 |
0.318 |
|
| 2018 |
Armstrong AJ, Gupta S, Healy P, Kemeny G, Leith LB, Zalutsky M, Spritzer C, Davies C, Ware K, Somarelli J, Wood K, Glover W, Hsu SD, Gerber D, Rothwell C, ... ... Gregory S, et al. Genomic and phenotypic evidence for prostate cancer osteomimicry in circulating tumor cells from men with metastatic castration resistant prostate cancer (mCRPC) treated with radium-223. Journal of Clinical Oncology. 36: 160-160. DOI: 10.1200/Jco.2018.36.6_Suppl.160 |
0.315 |
|
| 2017 |
Afshari NA, Igo RP, Morris NJ, Stambolian D, Sharma S, Pulagam VL, Dunn S, Stamler JF, Truitt BJ, Rimmler J, Kuot A, Croasdale CR, Qin X, Burdon KP, Riazuddin SA, ... ... Gregory SG, et al. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications. 8: 14898. PMID 28358029 DOI: 10.1038/Ncomms14898 |
0.755 |
|
| 2016 |
Zeng Y, Nie C, Min J, Liu X, Li M, Chen H, Xu H, Wang M, Ni T, Li Y, Yan H, Zhang JP, Song C, Chi LQ, Wang HM, ... ... Gregory S, et al. Novel loci and pathways significantly associated with longevity. Scientific Reports. 6: 21243. PMID 26912274 DOI: 10.1038/Srep21243 |
0.413 |
|
| 2015 |
Kraus WE, Muoio DM, Stevens R, Craig D, Bain JR, Grass E, Haynes C, Kwee L, Qin X, Slentz DH, Krupp D, Muehlbauer M, Hauser ER, Gregory SG, Newgard CB, et al. Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Plos Genetics. 11: e1005553. PMID 26540294 DOI: 10.1371/Journal.Pgen.1005553 |
0.71 |
|
| 2015 |
Shah AA, Gregory SG, Krupp D, Feng S, Dorogi A, Haynes C, Grass E, Lin SS, Hauser ER, Kraus WE, Shah SH, Hughes GC. Epigenetic Profiling Identifies Novel Genes for Ascending Aortic Aneurysm Formation with Bicuspid Aortic Valves. The Heart Surgery Forum. 18: E134-9. PMID 26334848 DOI: 10.1532/Hsf.1247 |
0.682 |
|
| 2015 |
Lock EF, Soldano KL, Garrett ME, Cope H, Markunas CA, Fuchs H, Grant G, Dunson DB, Gregory SG, Ashley-Koch AE. Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. Bmc Genomics. 16: 11. PMID 25609184 DOI: 10.1186/S12864-014-1211-8 |
0.724 |
|
| 2014 |
Krupp DR, Soldano KL, Garrett ME, Cope H, Ashley-Koch AE, Gregory SG. Missing genetic risk in neural tube defects: can exome sequencing yield an insight? Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 642-6. PMID 25044326 DOI: 10.1002/bdra.23276 |
0.708 |
|
| 2014 |
Markunas CA, Lock E, Soldano K, Cope H, Ding CK, Enterline DS, Grant G, Fuchs H, Ashley-Koch AE, Gregory SG. Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics. Bmc Medical Genomics. 7: 39. PMID 24962150 DOI: 10.1186/1755-8794-7-39 |
0.719 |
|
| 2014 |
Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG. Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 55: 4577-84. PMID 24917144 DOI: 10.1167/Iovs.13-13517 |
0.728 |
|
| 2014 |
Markunas CA, Enterline DS, Dunlap K, Soldano K, Cope H, Stajich J, Grant G, Fuchs H, Gregory SG, Ashley-Koch AE. Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation. Annals of Human Genetics. 78: 1-12. PMID 24359474 DOI: 10.1111/Ahg.12041 |
0.754 |
|
| 2014 |
Li J, Beaver J, Bitting RL, Gregory S, Armstrong AJ. Genomic analysis of circulating tumor cells (CTCs) from men with metastatic castration resistant prostate cancer (mCRPC) in the context of enzalutamide therapy. Journal of Clinical Oncology. 32: 5042-5042. DOI: 10.1200/Jco.2014.32.4_Suppl.65 |
0.312 |
|
| 2013 |
Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG. Genetic screen of African Americans with Fuchs endothelial corneal dystrophy. Molecular Vision. 19: 2508-16. PMID 24348007 |
0.733 |
|
| 2013 |
Soldano KL, Garrett ME, Cope HL, Rusnak JM, Ellis NJ, Dunlap KL, Speer MC, Gregory SG, Ashley-Koch AE. Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype. Birth Defects Research. Part B, Developmental and Reproductive Toxicology. 98: 365-73. PMID 24323870 DOI: 10.1002/Bdrb.21079 |
0.336 |
|
| 2013 |
Nolan D, Kraus WE, Hauser E, Li YJ, Thompson DK, Johnson J, Chen HC, Nelson S, Haynes C, Gregory SG, Kraus VB, Shah SH. Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family. Plos One. 8: e71779. PMID 23936524 DOI: 10.1371/Journal.Pone.0071779 |
0.355 |
|
| 2013 |
Connelly JJ, Cherepanova OA, Doss JF, Karaoli T, Lillard TS, Markunas CA, Nelson S, Wang T, Ellis PD, Langford CF, Haynes C, Seo DM, Goldschmidt-Clermont PJ, Shah SH, Kraus WE, ... ... Gregory SG, et al. Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis. Human Molecular Genetics. 22: 5107-20. PMID 23912340 DOI: 10.1093/Hmg/Ddt365 |
0.739 |
|
| 2013 |
Markunas CA, Soldano K, Dunlap K, Cope H, Asiimwe E, Stajich J, Enterline D, Grant G, Fuchs H, Gregory SG, Ashley-Koch AE. Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates. Plos One. 8: e61521. PMID 23620759 DOI: 10.1371/Journal.Pone.0061521 |
0.759 |
|
| 2012 |
Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG. Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE). Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 683-92. PMID 22806986 DOI: 10.1002/Bdra.23040 |
0.677 |
|
| 2012 |
Markunas CA, Tubbs RS, Moftakhar R, Ashley-Koch AE, Gregory SG, Oakes WJ, Speer MC, Iskandar BJ. Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations. Journal of Neurosurgery. Pediatrics. 9: 372-8. PMID 22462700 DOI: 10.3171/2011.12.PEDS11113 |
0.708 |
|
| 2012 |
Lin N, Di C, Bortoff K, Fu J, Truszkowski P, Killela P, Duncan C, McLendon R, Bigner D, Gregory S, Adamson DC. Deletion or epigenetic silencing of AJAP1 on 1p36 in glioblastoma. Molecular Cancer Research : McR. 10: 208-17. PMID 22241217 DOI: 10.1158/1541-7786.Mcr-10-0109 |
0.348 |
|
| 2011 |
Li YJ, Minear MA, Rimmler J, Zhao B, Balajonda E, Hauser MA, Allingham RR, Eghrari AO, Riazuddin SA, Katsanis N, Gottsch JD, Gregory SG, Klintworth GK, Afshari NA. Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Plos One. 6: e18044. PMID 21533127 DOI: 10.1371/Journal.Pone.0018044 |
0.762 |
|
| 2011 |
Minear MA, Crosslin DR, Sutton BS, Connelly JJ, Nelson SC, Gadson-Watson S, Wang T, Seo D, Vance JM, Sketch MH, Haynes C, Goldschmidt-Clermont PJ, Shah SH, Kraus WE, Hauser ER, ... Gregory SG, et al. Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. Human Genetics. 129: 641-54. PMID 21298289 DOI: 10.1007/S00439-011-0959-Z |
0.729 |
|
| 2010 |
Duncan CG, Killela PJ, Payne CA, Lampson B, Chen WC, Liu J, Solomon D, Waldman T, Towers AJ, Gregory SG, McDonald KL, McLendon RE, Bigner DD, Yan H. Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genes. Oncotarget. 1: 265-77. PMID 21113414 DOI: 10.18632/Oncotarget.137 |
0.306 |
|
| 2010 |
Fraser HI, Dendrou CA, Healy B, Rainbow DB, Howlett S, Smink LJ, Gregory S, Steward CA, Todd JA, Peterson LB, Wicker LS. Nonobese diabetic congenic strain analysis of autoimmune diabetes reveals genetic complexity of the Idd18 locus and identifies Vav3 as a candidate gene. Journal of Immunology (Baltimore, Md. : 1950). 184: 5075-84. PMID 20363978 DOI: 10.4049/Jimmunol.0903734 |
0.389 |
|
| 2010 |
Chen HC, Kraus VB, Li YJ, Nelson S, Haynes C, Johnson J, Stabler T, Hauser ER, Gregory SG, Kraus WE, Shah SH. Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family. Arthritis and Rheumatism. 62: 781-90. PMID 20187133 DOI: 10.1002/Art.27288 |
0.328 |
|
| 2010 |
Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN, Eghrari AO, Minear MA, Li YJ, Klintworth GK, Afshari N, Gregory SG, Gottsch JD, Katsanis N. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. American Journal of Human Genetics. 86: 45-53. PMID 20036349 DOI: 10.1016/J.Ajhg.2009.12.001 |
0.749 |
|
| 2009 |
Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA, Lintas C, Abramson RK, Wright HH, Ellis P, Langford CF, Worley G, Delong GR, Murphy SK, Cuccaro ML, et al. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. Bmc Medicine. 7: 62. PMID 19845972 DOI: 10.1186/1741-7015-7-62 |
0.727 |
|
| 2009 |
Crosslin DR, Shah SH, Nelson SC, Haynes CS, Connelly JJ, Gadson S, Goldschmidt-Clermont PJ, Vance JM, Rose J, Granger CB, Seo D, Gregory SG, Kraus WE, Hauser ER. Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis. Human Genetics. 125: 217-29. PMID 19130089 DOI: 10.1007/S00439-008-0619-0 |
0.344 |
|
| 2009 |
Afshari NA, Li YJ, Pericak-Vance MA, Gregory S, Klintworth GK. Genome-wide linkage scan in fuchs endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 50: 1093-7. PMID 18502986 DOI: 10.1167/Iovs.08-1839 |
0.464 |
|
| 2008 |
Deak KL, Siegel DG, George TM, Gregory S, Ashley-Koch A, Speer MC. Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 662-9. PMID 18937341 DOI: 10.1002/Bdra.20511 |
0.352 |
|
| 2008 |
Kennerly E, Ballmann A, Martin S, Wolfinger R, Gregory S, Stoskopf M, Gibson G. A gene expression signature of confinement in peripheral blood of red wolves (Canis rufus). Molecular Ecology. 17: 2782-91. PMID 18466232 DOI: 10.1111/J.1365-294X.2008.03775.X |
0.314 |
|
| 2008 |
Stamm DS, Siegel DG, Mehltretter L, Connelly JJ, Trott A, Ellis N, Zismann V, Stephan DA, George TM, Vekemans M, Ashley-Koch A, Gilbert JR, Gregory SG, Speer MC. Refinement of 2q and 7p loci in a large multiplex NTD family. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 441-52. PMID 18452155 DOI: 10.1002/Bdra.20462 |
0.31 |
|
| 2008 |
Sutton BS, Crosslin DR, Shah SH, Nelson SC, Bassil A, Hale AB, Haynes C, Goldschmidt-Clermont PJ, Vance JM, Seo D, Kraus WE, Gregory SG, Hauser ER. Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets. Human Molecular Genetics. 17: 1318-28. PMID 18204052 DOI: 10.1093/Hmg/Ddn020 |
0.306 |
|
| 2007 |
McCauley JL, Kenealy SJ, Margulies EH, Schnetz-Boutaud N, Gregory SG, Hauser SL, Oksenberg JR, Pericak-Vance MA, Haines JL, Mortlock DP. SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach. Bmc Genomics. 8: 266. PMID 17683615 DOI: 10.1186/1471-2164-8-266 |
0.318 |
|
| 2007 |
Gregory SG, Schmidt S, Seth P, Oksenberg JR, Hart J, Prokop A, Caillier SJ, Ban M, Goris A, Barcellos LF, Lincoln R, McCauley JL, Sawcer SJ, Compston DA, Dubois B, et al. Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Nature Genetics. 39: 1083-91. PMID 17660817 DOI: 10.1038/Ng2103 |
0.335 |
|
| 2007 |
Motsinger AA, Brassat D, Caillier SJ, Erlich HA, Walker K, Steiner LL, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes. Neurogenetics. 8: 11-20. PMID 17024427 DOI: 10.1007/S10048-006-0058-9 |
0.389 |
|
| 2006 |
de Bakker PI, McVean G, Sabeti PC, Miretti MM, Green T, Marchini J, Ke X, Monsuur AJ, Whittaker P, Delgado M, Morrison J, Richardson A, Walsh EC, Gao X, Galver L, ... ... Gregory S, et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nature Genetics. 38: 1166-72. PMID 16998491 DOI: 10.1038/Ng1885 |
0.383 |
|
| 2006 |
Natrajan R, Williams RD, Hing SN, Mackay A, Reis-Filho JS, Fenwick K, Iravani M, Valgeirsson H, Grigoriadis A, Langford CF, Dovey O, Gregory SG, Weber BL, Ashworth A, Grundy PE, et al. Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse Journal of Pathology. 210: 49-58. PMID 16823893 DOI: 10.1002/Path.2021 |
0.314 |
|
| 2006 |
Brassat D, Motsinger AA, Caillier SJ, Erlich HA, Walker K, Steiner LL, Cree BA, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans. Genes and Immunity. 7: 310-5. PMID 16625214 DOI: 10.1038/Sj.Gene.6364299 |
0.393 |
|
| 2005 |
Xu H, Gregory SG, Hauser ER, Stenger JE, Pericak-Vance MA, Vance JM, Züchner S, Hauser MA. SNPselector: a web tool for selecting SNPs for genetic association studies. Bioinformatics (Oxford, England). 21: 4181-6. PMID 16179360 DOI: 10.1093/Bioinformatics/Bti682 |
0.301 |
|
| 2005 |
Wicker LS, Moule CL, Fraser H, Penha-Goncalves C, Rainbow D, Garner VE, Chamberlain G, Hunter K, Howlett S, Clark J, Gonzalez-Munoz A, Cumiskey AM, Tiffen P, Howson J, Healy B, ... ... Gregory S, et al. Natural genetic variants influencing type 1 diabetes in humans and in the NOD mouse. Novartis Foundation Symposium. 267: 57-65; discussion 65. PMID 15999801 DOI: 10.1002/047002139X.Ch6 |
0.376 |
|
| 2005 |
Natrajan R, Williams R, Hing S, Little S, Mackay A, Reis-Filho J, Fenwick K, Iravani M, Valgeirsson H, Grigoriadis A, Langford C, Dovey O, Gregory S, Weber B, Ashworth A, et al. P43: Genomic changes in favourable histology Wilms tumours analysed by genome-wide 1 Mb-spaced and chromosome 1 tiling-path array CGH European Journal of Medical Genetics. 48: 507-508. DOI: 10.1016/J.Ejmg.2005.10.082 |
0.331 |
|
| 2004 |
Mallon AM, Wilming L, Weekes J, Gilbert JG, Ashurst J, Peyrefitte S, Matthews L, Cadman M, McKeone R, Sellick CA, Arkell R, Botcherby MR, Strivens MA, Campbell RD, Gregory S, et al. Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouse. Genome Research. 14: 1888-901. PMID 15364904 DOI: 10.1101/Gr.2478604 |
0.426 |
|
| 2004 |
Wicker LS, Chamberlain G, Hunter K, Rainbow D, Howlett S, Tiffen P, Clark J, Gonzalez-Munoz A, Cumiskey AM, Rosa RL, Howson JM, Smink LJ, Kingsnorth A, Lyons PA, Gregory S, et al. Fine mapping, gene content, comparative sequencing, and expression analyses support Ctla4 and Nramp1 as candidates for Idd5.1 and Idd5.2 in the nonobese diabetic mouse. Journal of Immunology (Baltimore, Md. : 1950). 173: 164-73. PMID 15210771 DOI: 10.4049/Jimmunol.173.1.164 |
0.406 |
|
| 2003 |
Penha-Gonçalves C, Moule C, Smink LJ, Howson J, Gregory S, Rogers J, Lyons PA, Suttie JJ, Lord CJ, Peterson LB, Todd JA, Wicker LS. Identification of a structurally distinct CD101 molecule encoded in the 950-kb Idd10 region of NOD mice. Diabetes. 52: 1551-6. PMID 12765969 DOI: 10.2337/Diabetes.52.6.1551 |
0.318 |
|
| 2003 |
Ueda H, Howson JM, Esposito L, Heward J, Snook H, Chamberlain G, Rainbow DB, Hunter KM, Smith AN, Di Genova G, Herr MH, Dahlman I, Payne F, Smyth D, Lowe C, ... ... Gregory S, et al. Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature. 423: 506-11. PMID 12724780 DOI: 10.1038/Nature01621 |
0.411 |
|
| 2002 |
Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, ... ... Gregory S, et al. Initial sequencing and comparative analysis of the mouse genome. Nature. 420: 520-62. PMID 12466850 DOI: 10.1038/Nature01262 |
0.349 |
|
| 2002 |
Parvari R, Hershkovitz E, Grossman N, Gorodischer R, Loeys B, Zecic A, Mortier G, Gregory S, Sharony R, Kambouris M, Sakati N, Meyer BF, Al Aqeel AI, Al Humaidan AK, Al Zanhrani F, et al. Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. Nature Genetics. 32: 448-52. PMID 12389028 DOI: 10.1038/Ng1012 |
0.344 |
|
| 2001 |
Stover C, Endo Y, Takahashi M, Lynch N, Constantinescu C, Vorup-Jensen T, Thiel S, Friedl H, Hankeln T, Hall R, Gregory S, Fujita T, Schwaeble W. The human gene for mannan binding lectin-associated serine protease-2 (MASP-2), the effector component of the lectin route of complement activation, is part of a tightly linked gene cluster on chromosome 1p36.2-3 Genes and Immunity. 2: 119-127. PMID 11426320 DOI: 10.1038/Sj.Gene.6363745 |
0.346 |
|
| 2001 |
Doudney K, Murdoch JN, Paternotte C, Bentley L, Gregory S, Copp AJ, Stanier P. Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23. Genomics. 72: 180-92. PMID 11401431 DOI: 10.1006/Geno.2000.6463 |
0.352 |
|
| 2001 |
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, ... ... Gregory S, et al. Initial sequencing and analysis of the human genome. Nature. 409: 860-921. PMID 11237011 DOI: 10.1038/35057062 |
0.311 |
|
| 2001 |
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, Fitzhugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, ... ... Gregory S, et al. Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) Nature. 412: 565-566. DOI: 10.1038/35087627 |
0.304 |
|
| 2001 |
Gregory S, Gilbert J. UNIT 1.3 Strategies for Genotype Generation Current Protocols in Human Genetics. DOI: 10.1002/0471142905.Hg0103S20 |
0.426 |
|
| 2000 |
Shackleton S, Lloyd DJ, Jackson SN, Evans R, Niermeijer MF, Singh BM, Schmidt H, Brabant G, Kumar S, Durrington PN, Gregory S, O'Rahilly S, Trembath RC. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nature Genetics. 24: 153-6. PMID 10655060 DOI: 10.1038/72807 |
0.357 |
|
| 1999 |
Gregory S, Gilbert J. Strategies for Genotype Generation Current Protocols in Human Genetics. 20. PMID 18428371 DOI: 10.1002/0471142905.Hg0103S47 |
0.416 |
|
| 1999 |
Labay V, Raz T, Baron D, Mandel H, Williams H, Barrett T, Szargel R, McDonald L, Shalata A, Nosaka K, Gregory S, Cohen N. Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Nature Genetics. 22: 300-4. PMID 10391221 DOI: 10.1038/10372 |
0.397 |
|
| 1996 |
Vosse Evd, Bergen A, Meershoek E, Oosterwijk J, Gregory S, Bakker B, Weissenbach J, Coffey A, vanOmmen G, DenDunnen J. An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS. European Journal of Human Genetics. 4: 101-104. PMID 8744027 DOI: 10.1159/000472177 |
0.401 |
|
| 1995 |
Fantes JA, Oghene K, Boyle S, Danes S, Fletcher JM, Bruford EA, Williamson K, Seawright A, Schedl A, Hanson I, Zehetner G, Bhogal R, Lehrach H, Gregory S, Williams J, et al. A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1 Genomics. 25: 447-461. PMID 7789978 DOI: 10.1016/0888-7543(95)80045-N |
0.349 |
|
| 1994 |
Redeker E, Hoovers JM, Alders M, van Moorsel CJ, Ivens AC, Gregory S, Kalikin L, Bliek J, de Galan L, van den Bogaard R. An integrated physical map of 210 markers assigned to the short arm of human chromosome 11. Genomics. 21: 538-50. PMID 7959730 DOI: 10.1006/Geno.1994.1312 |
0.321 |
|
| 1992 |
Heding IJJP, Ivens AC, Wilson J, Strivens M, Gregory S, Hoovers JMN, Mannens M, Redeker B, Porteous D, Heyningen Vv, Little PFR. The generation of ordered sets of cosmid DNA clones from human chromosome region 11p Genomics. 13: 89-94. PMID 1577496 DOI: 10.1016/0888-7543(92)90206-8 |
0.303 |
|
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