| Year |
Citation |
Score |
| 2022 |
Pacheco A, Issaian A, Davis J, Anderson N, Nemkov T, Paukovich N, Henen MA, Vögeli B, Sikela JM, Hansen K. Proteolytic activation of human-specific Olduvai domains by the furin protease. International Journal of Biological Macromolecules. PMID 36581038 DOI: 10.1016/j.ijbiomac.2022.12.260 |
0.432 |
|
| 2022 |
Paukovich N, Henen MA, Hussain A, Issaian A, Sikela JM, Hansen KC, Vögeli B. Solution NMR backbone assignments of disordered Olduvai protein domain CON1 employing Hα-detected experiments. Biomolecular Nmr Assignments. PMID 35098449 DOI: 10.1007/s12104-022-10068-5 |
0.308 |
|
| 2019 |
Heft IE, Mostovoy Y, Levy-Sakin M, Ma W, Stevens AJ, Pastor S, McCaffrey J, Boffelli D, Martin DI, Xiao M, Kennedy MA, Kwok PY, Sikela JM. The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome. Genetics. PMID 31754017 DOI: 10.1534/Genetics.119.302782 |
0.539 |
|
| 2019 |
Issaian A, Schmitt L, Born A, Nichols PJ, Sikela J, Hansen K, Vögeli B, Henen MA. Solution NMR backbone assignment reveals interaction-free tumbling of human lineage-specific Olduvai protein domains. Biomolecular Nmr Assignments. PMID 31264103 DOI: 10.1007/S12104-019-09902-0 |
0.386 |
|
| 2019 |
Fiddes IT, Pollen AA, Davis JM, Sikela JM. Paired involvement of human-specific Olduvai domains and NOTCH2NL genes in human brain evolution. Human Genetics. PMID 31087184 DOI: 10.1007/S00439-019-02018-4 |
0.513 |
|
| 2019 |
Issaian A, Hansen K, Vogeli B, Sikela J, Henen M. Human Lineage Specific 1 domain, NBPF15 Journal of Back and Musculoskeletal Rehabilitation. DOI: 10.13018/Bmr27569 |
0.383 |
|
| 2018 |
Sikela JM, Searles Quick VB. Genomic trade-offs: are autism and schizophrenia the steep price of the human brain? Human Genetics. 137: 1-13. PMID 29335774 DOI: 10.1007/s00439-017-1865-9 |
0.488 |
|
| 2017 |
Astling DP, Heft IE, Jones KL, Sikela JM. High resolution measurement of DUF1220 domain copy number from whole genome sequence data. Bmc Genomics. 18: 614. PMID 28807002 DOI: 10.1186/S12864-017-3976-Z |
0.468 |
|
| 2015 |
Sikela JM. Human evolutionary genomics and the search for the genes that made us human. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 479-81. PMID 25592606 |
0.432 |
|
| 2015 |
Keeney JG, O'Bleness MS, Anderson N, Davis JM, Arevalo N, Busquet N, Chick W, Rozman J, Hölter SM, Garrett L, Horsch M, Beckers J, Wurst W, Klingenspor M, ... ... Sikela JM, et al. Generation of mice lacking DUF1220 protein domains: effects on fecundity and hyperactivity. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 26: 33-42. PMID 25308000 DOI: 10.1007/S00335-014-9545-8 |
0.363 |
|
| 2015 |
Davis JM, Searles VB, Anderson N, Keeney J, Raznahan A, Horwood LJ, Fergusson DM, Kennedy MA, Giedd J, Sikela JM. DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores. Human Genetics. 134: 67-75. PMID 25287832 DOI: 10.1007/S00439-014-1489-2 |
0.345 |
|
| 2014 |
Carbone L, Harris RA, Gnerre S, Veeramah KR, Lorente-Galdos B, Huddleston J, Meyer TJ, Herrero J, Roos C, Aken B, Anaclerio F, Archidiacono N, Baker C, Barrell D, Batzer MA, ... ... Sikela JM, et al. Gibbon genome and the fast karyotype evolution of small apes. Nature. 513: 195-201. PMID 25209798 DOI: 10.1038/Nature13679 |
0.757 |
|
| 2014 |
Sikela JM. Finding and mapping new genes faster than ever: revisited. Genetics. 197: 1063-7. PMID 25104804 DOI: 10.1534/genetics.114.165373 |
0.357 |
|
| 2014 |
Keeney JG, Dumas L, Sikela JM. The case for DUF1220 domain dosage as a primary contributor to anthropoid brain expansion. Frontiers in Human Neuroscience. 8: 427. PMID 25009482 DOI: 10.3389/Fnhum.2014.00427 |
0.733 |
|
| 2014 |
Keeney JG, Davis JM, Siegenthaler J, Post MD, Nielsen BS, Hopkins WD, Sikela JM. DUF1220 protein domains drive proliferation in human neural stem cells and are associated with increased cortical volume in anthropoid primates. Brain Structure & Function. PMID 24957859 DOI: 10.1007/S00429-014-0814-9 |
0.411 |
|
| 2014 |
O'Bleness M, Searles VB, Dickens CM, Astling D, Albracht D, Mak AC, Lai YY, Lin C, Chu C, Graves T, Kwok PY, Wilson RK, Sikela JM. Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome. Bmc Genomics. 15: 387. PMID 24885025 DOI: 10.1186/1471-2164-15-387 |
0.463 |
|
| 2014 |
Davis JM, Searles VB, Anderson N, Keeney J, Dumas L, Sikela JM. DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism. Plos Genetics. 10: e1004241. PMID 24651471 DOI: 10.1371/Journal.Pgen.1004241 |
0.721 |
|
| 2014 |
Dumas L, Dickens CM, Anderson N, Davis J, Bennett B, Radcliffe RA, Sikela JM. Exome sequencing and arrayCGH detection of gene sequence and copy number variation between ILS and ISS mouse strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 25: 235-43. PMID 24553828 DOI: 10.1007/S00335-014-9502-6 |
0.741 |
|
| 2012 |
O'Bleness M, Searles VB, Varki A, Gagneux P, Sikela JM. Evolution of genetic and genomic features unique to the human lineage. Nature Reviews. Genetics. 13: 853-66. PMID 23154808 DOI: 10.1038/Nrg3336 |
0.383 |
|
| 2012 |
O'Bleness MS, Dickens CM, Dumas LJ, Kehrer-Sawatzki H, Wyckoff GJ, Sikela JM. Evolutionary history and genome organization of DUF1220 protein domains. G3 (Bethesda, Md.). 2: 977-86. PMID 22973535 DOI: 10.1534/G3.112.003061 |
0.805 |
|
| 2012 |
Dumas LJ, O'Bleness MS, Davis JM, Dickens CM, Anderson N, Keeney JG, Jackson J, Sikela M, Raznahan A, Giedd J, Rapoport J, Nagamani SS, Erez A, Brunetti-Pierri N, Sugalski R, ... ... Sikela JM, et al. DUF1220-domain copy number implicated in human brain-size pathology and evolution. American Journal of Human Genetics. 91: 444-54. PMID 22901949 DOI: 10.1016/J.Ajhg.2012.07.016 |
0.753 |
|
| 2010 |
Karimpour-Fard A, Dumas L, Phang T, Sikela JM, Hunter LE. A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation. Human Genomics. 4: 421-7. PMID 20846932 DOI: 10.1186/1479-7364-4-6-421 |
0.716 |
|
| 2010 |
Coors ME, Glover JJ, Juengst ET, Sikela JM. The ethics of using transgenic non-human primates to study what makes us human. Nature Reviews. Genetics. 11: 658-62. PMID 20717156 DOI: 10.1038/nrg2864 |
0.323 |
|
| 2009 |
Dumas L, Sikela JM. DUF1220 domains, cognitive disease, and human brain evolution. Cold Spring Harbor Symposia On Quantitative Biology. 74: 375-82. PMID 19850849 DOI: 10.1101/Sqb.2009.74.025 |
0.751 |
|
| 2007 |
Babcock M, Yatsenko S, Hopkins J, Brenton M, Cao Q, de Jong P, Stankiewicz P, Lupski JR, Sikela JM, Morrow BE. Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome. Human Molecular Genetics. 16: 2560-71. PMID 17675367 DOI: 10.1093/Hmg/Ddm197 |
0.439 |
|
| 2007 |
Dumas L, Kim YH, Karimpour-Fard A, Cox M, Hopkins J, Pollack JR, Sikela JM. Gene copy number variation spanning 60 million years of human and primate evolution. Genome Research. 17: 1266-77. PMID 17666543 DOI: 10.1101/Gr.6557307 |
0.783 |
|
| 2007 |
Gibbs RA, Rogers J, Katze MG, Bumgarner R, Weinstock GM, Mardis ER, Remington KA, Strausberg RL, Venter JC, Wilson RK, Batzer MA, Bustamante CD, Eichler EE, Hahn MW, ... ... Sikela JM, et al. Evolutionary and biomedical insights from the rhesus macaque genome. Science (New York, N.Y.). 316: 222-34. PMID 17431167 DOI: 10.1126/Science.1139247 |
0.753 |
|
| 2006 |
Popesco MC, Maclaren EJ, Hopkins J, Dumas L, Cox M, Meltesen L, McGavran L, Wyckoff GJ, Sikela JM. Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains. Science (New York, N.Y.). 313: 1304-7. PMID 16946073 DOI: 10.1126/Science.1127980 |
0.725 |
|
| 2006 |
Sikela JM. The jewels of our genome: the search for the genomic changes underlying the evolutionarily unique capacities of the human brain. Plos Genetics. 2: e80. PMID 16733552 DOI: 10.1371/journal.pgen.0020080 |
0.421 |
|
| 2006 |
Sikela JM, Maclaren EJ, Kim Y, Karimpour-Fard A, Cai WW, Pollack J, Hitzemann R, Belknap J, McWeeney S, Kerns RT, Downing C, Johnson TE, Grant KJ, Tabakoff B, Hoffman P, et al. DNA microarray and proteomic strategies for understanding alcohol action. Alcoholism, Clinical and Experimental Research. 30: 700-8. PMID 16573589 DOI: 10.1111/J.1530-0277.2006.00081.X |
0.757 |
|
| 2006 |
MacLaren EJ, Bennett B, Johnson TE, Sikela JM. Expression profiling identifies novel candidate genes for ethanol sensitivity QTLs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 147-56. PMID 16465594 DOI: 10.1007/S00335-005-0065-4 |
0.78 |
|
| 2005 |
MacLaren EJ, Sikela JM. Cerebellar gene expression profiling and eQTL analysis in inbred mouse strains selected for ethanol sensitivity. Alcoholism, Clinical and Experimental Research. 29: 1568-79. PMID 16205357 DOI: 10.1097/01.Alc.0000179376.27331.Ac |
0.782 |
|
| 2005 |
Kerns RT, Ravindranathan A, Hassan S, Cage MP, York T, Sikela JM, Williams RW, Miles MF. Ethanol-responsive brain region expression networks: implications for behavioral responses to acute ethanol in DBA/2J versus C57BL/6J mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 2255-66. PMID 15745951 DOI: 10.1523/JNEUROSCI.4372-04.2005 |
0.348 |
|
| 2004 |
Fortna A, Kim Y, MacLaren E, Marshall K, Hahn G, Meltesen L, Brenton M, Hink R, Burgers S, Hernandez-Boussard T, Karimpour-Fard A, Glueck D, McGavran L, Berry R, Pollack J, ... Sikela JM, et al. Lineage-specific gene duplication and loss in human and great ape evolution. Plos Biology. 2: E207. PMID 15252450 DOI: 10.1371/Journal.Pbio.0020207 |
0.799 |
|
| 2003 |
Hitzemann R, Malmanger B, Reed C, Lawler M, Hitzemann B, Coulombe S, Buck K, Rademacher B, Walter N, Polyakov Y, Sikela J, Gensler B, Burgers S, Williams RW, Manly K, et al. A strategy for the integration of QTL, gene expression, and sequence analyses. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 733-47. PMID 14722723 DOI: 10.1007/S00335-003-2277-9 |
0.434 |
|
| 2002 |
Ehringer MA, Thompson J, Conroy O, Goldman D, Smith TL, Schuckit MA, Sikela JM. Human alcoholism studies of genes identified through mouse quantitative trait locus analysis. Addiction Biology. 7: 365-71. PMID 14578011 DOI: 10.1080/1355621021000005496 |
0.382 |
|
| 2002 |
Ehringer MA, Sikela JM. Genomic approaches to the genetics of alcoholism. Alcohol Research & Health : the Journal of the National Institute On Alcohol Abuse and Alcoholism. 26: 181-92. PMID 12875046 |
0.337 |
|
| 2002 |
Marshall KE, Godden EL, Yang F, Burgers S, Buck KJ, Sikela JM. In silico discovery of gene-coding variants in murine quantitative trait loci using strain-specific genome sequence databases. Genome Biology. 3: RESEARCH0078. PMID 12537567 DOI: 10.1186/Gb-2002-3-12-Research0078 |
0.413 |
|
| 2002 |
Ehringer MA, Thompson J, Conroy O, Yang F, Hink R, Bennett B, Johnson TE, Sikela JM. Fine mapping of polymorphic alcohol-related quantitative trait loci candidate genes using interval-specific congenic recombinant mice. Alcoholism, Clinical and Experimental Research. 26: 1603-8. PMID 12436047 DOI: 10.1111/J.1530-0277.2002.Tb02461.X |
0.381 |
|
| 2002 |
Kirstein SL, Davidson KL, Ehringer MA, Sikela JM, Erwin VG, Tabakoff B. Quantitative trait loci affecting initial sensitivity and acute functional tolerance to ethanol-induced ataxia and brain cAMP signaling in BXD recombinant inbred mice. The Journal of Pharmacology and Experimental Therapeutics. 302: 1238-45. PMID 12183685 DOI: 10.1124/Jpet.302.3.1238 |
0.35 |
|
| 2001 |
Ehringer MA, Thompson J, Conroy O, Xu Y, Yang F, Canniff J, Beeson M, Gordon L, Bennett B, Johnson TE, Sikela JM. High-throughput sequence identification of gene coding variants within alcohol-related QTLs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 657-63. PMID 11471062 DOI: 10.1007/S00335-001-1001-X |
0.349 |
|
| 2001 |
Xu Y, Ehringer M, Yang F, Sikela JM. Comparison of global brain gene expression profiles between inbred long-sleep and inbred short-sleep mice by high-density gene array hybridization. Alcoholism, Clinical and Experimental Research. 25: 810-8. PMID 11410715 DOI: 10.1111/J.1530-0277.2001.Tb02284.X |
0.366 |
|
| 2000 |
Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract. Investigative Ophthalmology & Visual Science. 41: 3278-85. PMID 11006214 |
0.341 |
|
| 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, ... ... Sikela JM, 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 |
0.377 |
|
| 1997 |
Brady KP, Rowe LB, Her H, Stevens TJ, Eppig J, Sussman DJ, Sikela J, Beier DR. Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Research. 7: 1085-93. PMID 9371744 DOI: 10.1101/Gr.7.11.1085 |
0.405 |
|
| 1997 |
Sjøholt G, Molven A, Løvlie R, Wilcox A, Sikela JM, Steen VM. Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). Genomics. 45: 113-22. PMID 9339367 DOI: 10.1006/geno.1997.4862 |
0.393 |
|
| 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, ... ... Sikela JM, 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 |
0.402 |
|
| 1996 |
Gordon DF, Wagner J, Atkinson BL, Chiono M, Berry R, Sikela J, Gutierrez-Hartmann A. Human Cart-1: structural organization, chromosomal localization, and functional analysis of a cartilage-specific homeodomain cDNA. Dna and Cell Biology. 15: 531-41. PMID 8756334 DOI: 10.1089/Dna.1996.15.531 |
0.331 |
|
| 1996 |
Orlicky DJ, Berry R, Sikela JM. Human chromosome 1 localization of the gene for a prostaglandin F2alpha receptor negative regulatory protein. Human Genetics. 97: 655-8. PMID 8655148 |
0.328 |
|
| 1995 |
Hellevuo K, Berry R, Sikela JM, Tabakoff B. Localization of the gene for a novel human adenylyl cyclase (ADCY7) to chromosome 16. Human Genetics. 95: 197-200. PMID 7860067 DOI: 10.1007/Bf00209401 |
0.388 |
|
| 1995 |
Berry R, Stevens TJ, Walter NA, Wilcox AS, Rubano T, Hopkins JA, Weber J, Goold R, Soares MB, Sikela JM. Gene-based sequence-tagged-sites (STSs) as the basis for a human gene map. Nature Genetics. 10: 415-23. PMID 7670491 DOI: 10.1038/Ng0895-415 |
0.473 |
|
| 1995 |
Renouf S, Beullens M, Wera S, Van Eynde A, Sikela J, Stalmans W, Bollen M. Molecular cloning of a human polypeptide related to yeast sds22, a regulator of protein phosphatase-1. Febs Letters. 375: 75-8. PMID 7498485 DOI: 10.1016/0014-5793(95)01180-M |
0.377 |
|
| 1995 |
Berry R, Walter NA, Stevens TJ, Rubano T, Wilcox AS, Hopkins JA, Sikela JM. A strategy for the identification of candidate genes for alcohol-related phenotypes and other human disorders using rapid polymerase chain reaction mapping of gene-based sequence-tagged sites. Alcoholism, Clinical and Experimental Research. 19: 821-3. PMID 7485825 DOI: 10.1111/j.1530-0277.1995.tb00952.x |
0.462 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Sikela JM, Adams M, Venter JC, Merril CR. Chromosomal distribution of 320 genes from a brain cDNA library. Nature Genetics. 4: 381-6. PMID 8401586 DOI: 10.1038/Ng0893-381 |
0.401 |
|
| 1992 |
Khan AS, Wilcox AS, Polymeropoulos MH, Hopkins JA, Stevens TJ, Robinson M, Orpana AK, Sikela JM. Single pass sequencing and physical and genetic mapping of human brain cDNAs. Nature Genetics. 2: 180-5. PMID 1345165 DOI: 10.1038/Ng1192-180 |
0.39 |
|
| 1992 |
Wilcox AS, Warrington JA, Gardiner K, Berger R, Whiting P, Altherr MR, Wasmuth JJ, Patterson D, Sikela JM. Human chromosomal localization of genes encoding the gamma 1 and gamma 2 subunits of the gamma-aminobutyric acid receptor indicates that members of this gene family are often clustered in the genome. Proceedings of the National Academy of Sciences of the United States of America. 89: 5857-61. PMID 1321425 DOI: 10.1073/Pnas.89.13.5857 |
0.391 |
|
| 1991 |
Wilcox AS, Khan AS, Hopkins JA, Sikela JM. Use of 3' untranslated sequences of human cDNAs for rapid chromosome assignment and conversion to STSs: implications for an expression map of the genome. Nucleic Acids Research. 19: 1837-43. PMID 2030965 DOI: 10.1093/nar/19.8.1837 |
0.45 |
|
| 1989 |
Sikela JM, Law ML, Kao FT, Hartz JA, Wei Q, Hahn WE. Chromosomal localization of the human gene for brain Ca2+/calmodulin-dependent protein kinase type IV. Genomics. 4: 21-7. PMID 2536634 DOI: 10.1016/0888-7543(89)90309-1 |
0.341 |
|
| 1985 |
Dush MK, Sikela JM, Khan SA, Tischfield JA, Stambrook PJ. Nucleotide sequence and organization of the mouse adenine phosphoribosyltransferase gene: presence of a coding region common to animal and bacterial phosphoribosyltransferases that has a variable intron/exon arrangement. Proceedings of the National Academy of Sciences of the United States of America. 82: 2731-5. PMID 3921964 DOI: 10.1073/pnas.82.9.2731 |
0.345 |
|
| 1983 |
Sikela JM, Khan SA, Feliciano E, Trill J, Tischfield JA, Stambrook PJ. Cloning and expression of a mouse adenine phosphoribosyltransferase gene. Gene. 22: 219-28. PMID 6307822 DOI: 10.1016/0378-1119(83)90106-3 |
0.306 |
|
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