| Year |
Citation |
Score |
| 2020 |
Markunas CA, Hancock DB, Xu Z, Quach BC, Fang F, Sandler DP, Johnson EO, Taylor JA. Epigenome-wide analysis uncovers a blood-based DNA methylation biomarker of lifetime cannabis use. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32803843 DOI: 10.1002/Ajmg.B.32813 |
0.352 |
|
| 2020 |
Markunas CA, Semick SA, Quach BC, Tao R, Deep-Soboslay A, Carnes MU, Bierut LJ, Hyde TM, Kleinman JE, Johnson EO, Jaffe AE, Hancock DB. Genome-wide DNA methylation differences in nucleus accumbens of smokers vs. nonsmokers. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 32731254 DOI: 10.1038/S41386-020-0782-0 |
0.341 |
|
| 2019 |
Sikdar S, Joehanes R, Joubert BR, Xu CJ, Vives-Usano M, Rezwan FI, Felix JF, Ward JM, Guan W, Richmond RC, Brody JA, Küpers LK, Baïz N, Håberg SE, Smith JA, ... ... Markunas CA, et al. Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking. Epigenomics. PMID 31536415 DOI: 10.2217/Epi-2019-0066 |
0.339 |
|
| 2018 |
Semick SA, Collado-Torres L, Markunas CA, Shin JH, Deep-Soboslay A, Tao R, Huestis MA, Bierut LJ, Maher BS, Johnson EO, Hyde TM, Weinberger DR, Hancock DB, Kleinman JE, Jaffe AE. Developmental effects of maternal smoking during pregnancy on the human frontal cortex transcriptome. Molecular Psychiatry. PMID 30131587 DOI: 10.1038/S41380-018-0223-1 |
0.368 |
|
| 2018 |
Hancock DB, Markunas CA, Bierut LJ, Johnson EO. Human Genetics of Addiction: New Insights and Future Directions. Current Psychiatry Reports. 20: 8. PMID 29504045 DOI: 10.1007/S11920-018-0873-3 |
0.455 |
|
| 2017 |
Hancock DB, Guo Y, Reginsson GW, Gaddis NC, Lutz SM, Sherva R, Loukola A, Minica CC, Markunas CA, Han Y, Young KA, Gudbjartsson DF, Gu F, McNeil DW, Qaiser B, et al. Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Molecular Psychiatry. PMID 28972577 DOI: 10.1038/Mp.2017.193 |
0.382 |
|
| 2017 |
Markunas CA, Johnson EO, Hancock DB. Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants. Human Genetics. PMID 28567521 DOI: 10.1007/S00439-017-1815-6 |
0.397 |
|
| 2016 |
Markunas CA, Wilcox AJ, Xu Z, Joubert BR, Harlid S, Panduri V, Håberg SE, Nystad W, London SJ, Sandler DP, Lie RT, Wade PA, Taylor JA. Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults. Plos One. 11: e0156361. PMID 27383059 DOI: 10.1371/Journal.Pone.0156361 |
0.338 |
|
| 2016 |
Joubert BR, Felix JF, Yousefi P, Bakulski KM, Just AC, Breton C, Reese SE, Markunas CA, Richmond RC, Xu CJ, Küpers LK, Oh SS, Hoyo C, Gruzieva O, Söderhäll C, et al. DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis. American Journal of Human Genetics. PMID 27040690 DOI: 10.1016/J.Ajhg.2016.02.019 |
0.397 |
|
| 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 |
0.57 |
|
| 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 |
0.575 |
|
| 2014 |
Markunas CA, Xu Z, Harlid S, Wade PA, Lie RT, Taylor JA, Wilcox AJ. Identification of DNA methylation changes in newborns related to maternal smoking during pregnancy. Environmental Health Perspectives. 122: 1147-53. PMID 24906187 DOI: 10.1289/Ehp.1307892 |
0.32 |
|
| 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 |
0.603 |
|
| 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, 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 |
0.591 |
|
| 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 |
0.617 |
|
| 2013 |
Markunas CA, Ashley-Koch AE, Gregory SG. Genetics of the Chiari i and II malformations The Chiari Malformations. 2147483647: 93-101. DOI: 10.1007/978-1-4614-6369-6_7 |
0.342 |
|
| 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 |
0.519 |
|
| 2011 |
Rizzi TS, Arias-Vasquez A, Rommelse N, Kuntsi J, Anney R, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Ruano D, Van der Sluis S, Markunas CA, Garrett ME, Ashley-Koch AE, Kollins SH, et al. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 145-57. PMID 21302343 DOI: 10.1002/Ajmg.B.31149 |
0.443 |
|
| 2010 |
Markunas CA, Quinn KS, Collins AL, Garrett ME, Lachiewicz AM, Sommer JL, Morrissey-Kane E, Kollins SH, Anastopoulos AD, Ashley-Koch AE. Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families. Psychiatric Genetics. 20: 73-81. PMID 20032819 DOI: 10.1097/Ypg.0B013E3283351209 |
0.343 |
|
| 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 |
0.593 |
|
| 2008 |
Markunas CA, Umbach DM, Xu Z, Taylor JA. Assessing Candidate Gene nsSNPs for Phenotypic Differences in Double-Strand Break Repair Using Radiation-Induced gammaH2A.X Foci. Journal of Cancer Epidemiology. 2008: 387423. PMID 20445776 DOI: 10.1155/2008/387423 |
0.309 |
|
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