Assessing Candidate Gene nsSNPs for Phenotypic Differences in Double-Strand Break Repair Using Radiation-Induced γH2A.X Foci

Por Markunas, Christina A., Umbach, David M., Xu, Zongli, Taylor, Jack A.
Publicado em 2008

Human Genetics of Addiction: New Insights and Future Directions

Por Hancock, Dana B., Markunas, Christina A., Bierut, Laura J., Johnson, Eric O.
Publicado no Curr Psychiatry Rep (2018)

Identification of DNA Methylation Changes in Newborns Related to Maternal Smoking during Pregnancy

Por Markunas, Christina A., Xu, Zongli, Harlid, Sophia, Wade, Paul A., Lie, Rolv T., Taylor, Jack A., Wilcox, Allen J.
Publicado em 2014

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations

Por Markunas, Christina A., Tubbs, R. Shane, Moftakhar, Roham, Ashley-Koch, Allison E., Gregory, Simon G., Oakes, W. Jerry, Speer, Marcy C., Iskandar, Bermans J.
Publicado em 2012

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari Type I Malformation

Por MARKUNAS, CHRISTINA A., ENTERLINE, DAVID S., DUNLAP, KAITLYN, SOLDANO, KAREN, COPE, HEIDI, STAJICH, JEFFREY, GRANT, GERALD, FUCHS, HERBERT, GREGORY, SIMON G., ASHLEY-KOCH, ALLISON E.
Publicado em 2013

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

Por Markunas, Christina A., Soldano, Karen, Dunlap, Kaitlyn, Cope, Heidi, Asiimwe, Edgar, Stajich, Jeffrey, Enterline, David, Grant, Gerald, Fuchs, Herbert, Gregory, Simon G., Ashley-Koch, Allison E.
Publicado em 2013

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

Por Markunas, Christina A, Lock, Eric, Soldano, Karen, Cope, Heidi, Ding, Chien-Kuang C, Enterline, David S, Grant, Gerald, Fuchs, Herbert, Ashley-Koch, Allison E, Gregory, Simon G
Publicado em 2014

Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation

Por Lock, Eric F, Soldano, Karen L, Garrett, Melanie E, Cope, Heidi, Markunas, Christina A, Fuchs, Herbert, Grant, Gerald, Dunson, David B, Gregory, Simon G, Ashley-Koch, Allison E
Publicado no BMC Genomics (2015)

Genetic variants in SLC9A9 are associated with measures of Attention-deficit/hyperactivity disorder symptoms in families

Por Markunas, Christina A., Quinn, Kaia S., Collins, Ann L., Garrett, Melanie E., Lachiewicz, Ave M., Sommer, Jennifer L., Morrissey-Kane, Erin, Kollins, Scott H., Anastopoulos, Arthur D., Ashley-Koch, Allison E.
Publicado em 2010

Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults

Por Markunas, Christina A., Wilcox, Allen J., Xu, Zongli, Joubert, Bonnie R., Harlid, Sophia, Panduri, Vijayalakshmi, Håberg, Siri E., Nystad, Wenche, London, Stephanie J., Sandler, Dale P., Lie, Rolv T., Wade, Paul A., Taylor, Jack A.
Publicado no PLoS One (2016)

Genome-wide DNA methylation differences in nucleus accumbens of smokers vs. nonsmokers

Por Markunas, Christina A., Semick, Stephen A., Quach, Bryan C., Tao, Ran, Deep-Soboslay, Amy, Carnes, Megan U., Bierut, Laura J., Hyde, Thomas M., Kleinman, Joel E., Johnson, Eric O., Jaffe, Andrew E., Hancock, Dana B.
Publicado no Neuropsychopharmacology (2020)

Developmental effects of maternal smoking during pregnancy on the human frontal cortex transcriptome

Por Semick, Stephen A., Collado-Torres, Leonardo, Markunas, Christina A., Shin, Joo Heon, Deep-Soboslay, Amy, Tao, Ran, Huestis, Marilyn, Bierut, Laura J., Maher, Brion S., Johnson, Eric O., Hyde, Thomas M., Weinberger, Daniel R., Hancock, Dana B., Kleinman, Joel E., Jaffe, Andrew E.
Publicado no Mol Psychiatry (2018)

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Por Worley Gordon, Langford Cordelia F, Ellis Peter, Wright Harry H, Abramson Ruth K, Lintas Carla, Markunas Christina A, Biscocho Dhani, Johnson Jessica, Towers Aaron J, Connelly Jessica J, Gregory Simon G, Delong G Robert, Murphy Susan K, Cuccaro Michael L, Persico Antonello, Pericak-Vance Margaret A
Publicado em 2009-10-01

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Por Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A
Publicado em 2009

Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis

Por Connelly, Jessica J., Cherepanova, Olga A., Doss, Jennifer F., Karaoli, Themistoclis, Lillard, Travis S., Markunas, Christina A., Nelson, Sarah, Wang, Tianyuan, Ellis, Peter D., Langford, Cordelia F., Haynes, Carol, Seo, David M., Goldschmidt-Clermont, Pascal J., Shah, Svati H., Kraus, William E., Hauser, Elizabeth R., Gregory, Simon G.
Publicado em 2013

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

Por Hancock, Dana B., Guo, Yuelong, Reginsson, Gunnar W., Gaddis, Nathan C., Lutz, Sharon M., Sherva, Richard, Loukola, Anu, Minica, Camelia, Markunas, Christina A., Han, Younghun, Young, Kendra A., Gudbjartsson, Daniel F., Gu, Fangyi, McNeil, Daniel W., Qaiser, Beenish, Glasheen, Cristie, Olson, Sean, Landi, Maria Teresa, Madden, Pamela A. F., Farrer, Lindsay A., Vink, Jacqueline, Saccone, Nancy L., Neale, Michael C., Kranzler, Henry R., McKay, James, Hung, Rayjean J., Amos, Christopher I., Marazita, Mary L., Boomsma, Dorret I., Baker, Timothy B., Gelernter, Joel, Kaprio, Jaakko, Caporaso, Neil E., Thorgeirsson, Thorgeir E., Hokanson, John E., Bierut, Laura J., Stefansson, Kari, Johnson, Eric O.
Publicado no Mol Psychiatry (2017)

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

Por Rizzi, Thais S, Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, Van der Sluis, Sophie, Markunas, Christina A, Garrett, Melanie E, Ashley-Koch, Allison E, Kollins, Scott H, Anastopoulos, Arthur D, Hansell, Narelle K, Wright, Margaret J, Montgomery, Grant W, Martin, Nicholas G, Harris, Sarah E, Davies, Gail, Tenesa, Albert, Porteous, David J, Starr, John M, Deary, Ian J, St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J, Evans, David M, Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund, Steinhausen, Hans Christoph, Taylor, Eric, Faraone, Stephen V, Franke, Barbara, Posthuma, Danielle
Publicado em 2011

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

Por Quach, Bryan C., Bray, Michael J., Gaddis, Nathan C., Liu, Mengzhen, Palviainen, Teemu, Minica, Camelia C., Zellers, Stephanie, Sherva, Richard, Aliev, Fazil, Nothnagel, Michael, Young, Kendra A., Marks, Jesse A., Young, Hannah, Carnes, Megan U., Guo, Yuelong, Waldrop, Alex, Sey, Nancy Y. A., Landi, Maria T., McNeil, Daniel W., Drichel, Dmitriy, Farrer, Lindsay A., Markunas, Christina A., Vink, Jacqueline M., Hottenga, Jouke-Jan, Iacono, William G., Kranzler, Henry R., Saccone, Nancy L., Neale, Michael C., Madden, Pamela, Rietschel, Marcella, Marazita, Mary L., McGue, Matthew, Won, Hyejung, Winterer, Georg, Grucza, Richard, Dick, Danielle M., Gelernter, Joel, Caporaso, Neil E., Baker, Timothy B., Boomsma, Dorret I., Kaprio, Jaakko, Hokanson, John E., Vrieze, Scott, Bierut, Laura J., Johnson, Eric O., Hancock, Dana B.
Publicado no Nat Commun (2020)

Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10–Pulmonary Function Association

Por Xu, Jiayi, Gaddis, Nathan C., Bartz, Traci M., Hou, Ruixue, Manichaikul, Ani W., Pankratz, Nathan, Smith, Albert V., Sun, Fangui, Terzikhan, Natalie, Markunas, Christina A., Patchen, Bonnie K., Schu, Matthew, Beydoun, May A., Brusselle, Guy G., Eiriksdottir, Gudny, Zhou, Xia, Wood, Alexis C., Graff, Mariaelisa, Harris, Tamara B., Ikram, M. Arfan, Jacobs, David R., Launer, Lenore J., Lemaitre, Rozenn N., O’Connor, George T., Oelsner, Elizabeth C., Psaty, Bruce M., Vasan, Ramachandran S., Rohde, Rebecca R., Rich, Stephen S., Rotter, Jerome I., Seshadri, Sudha, Smith, Lewis J., Tiemeier, Henning, Tsai, Michael Y., Uitterlinden, André G., Voruganti, V. Saroja, Xu, Hanfei, Zilhão, Nuno R., Fornage, Myriam, Zillikens, M. Carola, London, Stephanie J., Barr, R. Graham, Dupuis, Josée, Gharib, Sina A., Gudnason, Vilmundur, Lahousse, Lies, North, Kari E., Steffen, Lyn M., Cassano, Patricia A., Hancock, Dana B.
Publicado no Am J Respir Crit Care Med (2019)

Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking

Por Sikdar, Sinjini, Joehanes, Roby, Joubert, Bonnie R, Xu, Cheng-Jian, Vives-Usano, Marta, Rezwan, Faisal I, Felix, Janine F, Ward, James M, Guan, Weihua, Richmond, Rebecca C, Brody, Jennifer A, Küpers, Leanne K, Baïz, Nour, Håberg, Siri E, Smith, Jennifer A, Reese, Sarah E, Aslibekyan, Stella, Hoyo, Cathrine, Dhingra, Radhika, Markunas, Christina A, Xu, Tao, Reynolds, Lindsay M, Just, Allan C, Mandaviya, Pooja R, Ghantous, Akram, Bennett, Brian D, Wang, Tianyuan, Consortium, The BIOS, Bakulski, Kelly M, Melen, Erik, Zhao, Shanshan, Jin, Jianping, Herceg, Zdenko, van Meurs, Joyce, Taylor, Jack A, Baccarelli, Andrea A, Murphy, Susan K, Liu, Yongmei, Munthe-Kaas, Monica Cheng, Deary, Ian J, Nystad, Wenche, Waldenberger, Melanie, Annesi-Maesano, Isabella, Conneely, Karen, Jaddoe, Vincent WV, Arnett, Donna, Snieder, Harold, Kardia, Sharon LR, Relton, Caroline L, Ong, Ken K, Ewart, Susan, Moreno-Macias, Hortensia, Romieu, Isabelle, Sotoodehnia, Nona, Fornage, Myriam, Motsinger-Reif, Alison, Koppelman, Gerard H, Bustamante, Mariona, Levy, Daniel, London, Stephanie J
Publicado no Epigenomics (2019)