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A Genome-Wide Copy Number Variant Study of Suicidal Behavior: e0128369
Gross, Jeffrey A, Bureau, Alexandre, Croteau, Jordie, Galfalvy, Hanga, Oquendo, Maria A, Haghighi, Fatemeh, Merette, Chantal, Giegling, Ina, Hodgkinson, Colin, Goldman, David
Published in PloS one (01.05.2015)
Published in PloS one (01.05.2015)
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FISH and SNP-Array Karyotyping Improve the Detection of Recurrent Chromosomal Defects Including Del(5q), Monosomy 7, Del(7q), Trisomy 8, and Del(20q) in Myelodysplastic Syndromes
Makishima, Hideki, Rataul, Manjot, Gondek, Lukasz P., Huh, Jungwon, Cook, James R., Theil, Karl S., Sekeres, Mikkael A, Kuczkowski, Elizabeth, Maciejewski, Jaroslaw P.
Published in Blood (16.11.2008)
Published in Blood (16.11.2008)
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The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations
Ahn, Myung-Ju, Won, Hong-Hee, Lee, Jeeyun, Lee, Seung-Tae, Sun, Jong-Mu, Park, Yeon Hee, Ahn, Jin Seok, Kwon, O Jung, Kim, Hojoong, Shim, Young Mog, Kim, Jhingook, Kim, Kwhanmien, Kim, Yeul Hong, Park, Jae Yong, Kim, Jong-Won, Park, Keunchil
Published in Human genetics (01.03.2012)
Published in Human genetics (01.03.2012)
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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
Liu, Ke, Kurien, Biji T., Zimmerman, Sarah L., Kaufman, Kenneth M., Taft, Diana H., Kottyan, Leah C., Lazaro, Sara, Weaver, Carrie A., Ice, John A., Adler, Adam J., Chodosh, James, Radfar, Lida, Rasmussen, Astrid, Stone, Donald U., Lewis, David M., Li, Shibo, Koelsch, Kristi A., Igoe, Ann, Talsania, Mitali, Kumar, Jay, Maier‐Moore, Jacen S., Harris, Valerie M., Gopalakrishnan, Rajaram, Jonsson, Roland, Lessard, James A., Lu, Xianglan, Gottenberg, Jacques‐Eric, Anaya, Juan‐Manuel, Cunninghame‐Graham, Deborah S., Huang, Andrew J. W., Brennan, Michael T., Hughes, Pamela, Illei, Gabor G., Miceli‐Richard, Corinne, Keystone, Edward C., Bykerk, Vivian P., Hirschfield, Gideon, Xie, Gang, Ng, Wan‐Fai, Nordmark, Gunnel, Eriksson, Per, Omdal, Roald, Rhodus, Nelson L., Rischmueller, Maureen, Rohrer, Michael, Segal, Barbara M., Vyse, Timothy J., Wahren‐Herlenius, Marie, Witte, Torsten, Pons‐Estel, Bernardo, Alarcón‐Riquelme, Marta E., Guthridge, Joel M., James, Judith A., Lessard, Christopher J., Kelly, Jennifer A., Thompson, Susan D., Gaffney, Patrick M., Montgomery, Courtney G., Edberg, Jeffrey C., Kimberly, Robert P., Alarcón, Graciela S., Langefeld, Carl L., Gilkeson, Gary S., Kamen, Diane L., Tsao, Betty P., Joseph McCune, W., Salmon, Jane E., Merrill, Joan T., Weisman, Michael H., Wallace, Daniel J., Utset, Tammy O., Bottinger, Erwin P., Amos, Christopher I., Siminovitch, Katherine A., Mariette, Xavier, Sivils, Kathy L., Harley, John B., Hal Scofield, R.
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.05.2016)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.05.2016)
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Large recurrent microdeletions associated with schizophrenia
Stefansson, Hreinn, Rujescu, Dan, Cichon, Sven, Pietiläinen, Olli P. H., Ingason, Andres, Steinberg, Stacy, Fossdal, Ragnheidur, Sigurdsson, Engilbert, Sigmundsson, Thordur, Buizer-Voskamp, Jacobine E., Hansen, Thomas, Jakobsen, Klaus D., Muglia, Pierandrea, Francks, Clyde, Matthews, Paul M., Gylfason, Arnaldur, Halldorsson, Bjarni V., Gudbjartsson, Daniel, Thorgeirsson, Thorgeir E., Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Bjornsson, Asgeir, Mattiasdottir, Sigurborg, Blondal, Thorarinn, Haraldsson, Magnus, Magnusdottir, Brynja B., Giegling, Ina, Möller, Hans-Jürgen, Hartmann, Annette, Shianna, Kevin V., Ge, Dongliang, Need, Anna C., Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamarie, Paunio, Tiina, Toulopoulou, Timi, Bramon, Elvira, Di Forti, Marta, Murray, Robin, Ruggeri, Mirella, Vassos, Evangelos, Tosato, Sarah, Walshe, Muriel, Li, Tao, Vasilescu, Catalina, Mühleisen, Thomas W., Wang, August G., Ullum, Henrik, Djurovic, Srdjan, Melle, Ingrid, Olesen, Jes, Kiemeney, Lambertus A., Franke, Barbara, Sabatti, Chiara, Freimer, Nelson B., Gulcher, Jeffrey R., Thorsteinsdottir, Unnur, Kong, Augustine, Andreassen, Ole A., Ophoff, Roel A., Georgi, Alexander, Rietschel, Marcella, Werge, Thomas, Petursson, Hannes, Goldstein, David B., Nöthen, Markus M., Peltonen, Leena, Collier, David A., St Clair, David, Stefansson, Kari
Published in Nature (11.09.2008)
Published in Nature (11.09.2008)
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Cytox launches breakthrough genetic biomarker research assay for Alzheimer's disease risk assessment
Published in Business Wire
(22.07.2016)
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Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly
Gonzaga-Jauregui, Claudia, Lotze, Timothy, Jamal, Leila, Penney, Samantha, Campbell, Ian M, Pehlivan, Davut, Hunter, Jill V, Woodbury, Suzanne L, Raymond, Gerald, Adesina, Adekunle M, Jhangiani, Shalini N, Reid, Jeffrey G, Muzny, Donna M, Boerwinkle, Eric, Lupski, James R, Gibbs, Richard A, Wiszniewski, Wojciech
Published in JAMA neurology (01.12.2013)
Published in JAMA neurology (01.12.2013)
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HLA class I alleles are associated with clinic-based migraine and increased risks of chronic migraine and medication overuse
Huang, Claire, Chen, Shih-Pin, Huang, Yu-Han, Chen, Hsuan-Yu, Wang, Yen-Feng, Lee, Mei-Hsuan, Wang, Shuu-Jiun
Published in Cephalalgia (01.04.2020)
Published in Cephalalgia (01.04.2020)
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A Novel Variant in CDKN1C Is Associated With Intrauterine Growth Restriction, Short Stature, and Early-Adulthood-Onset Diabetes
Kerns, Sarah L., Guevara-Aguirre, Jaime, Andrew, Shayne, Geng, Juan, Guevara, Carolina, Guevara-Aguirre, Marco, Guo, Michael, Oddoux, Carole, Shen, Yiping, Zurita, Andres, Rosenfeld, Ron G., Ostrer, Harry, Hwa, Vivian, Dauber, Andrew
Published in The journal of clinical endocrinology and metabolism (01.10.2014)
Published in The journal of clinical endocrinology and metabolism (01.10.2014)
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X Chromosome Dose and Sex Bias in Autoimmune Diseases
Liu, Ke, Kurien, Biji T., Zimmerman, Sarah L., Kaufman, Kenneth M., Taft, Diana H., Kottyan, Leah C., Lazaro, Sara, Weaver, Carrie A., Ice, John A., Adler, Adam J., Chodosh, James, Radfar, Lida, Rasmussen, Astrid, Stone, Donald U., Lewis, David M., Li, Shibo, Koelsch, Kristi A., Igoe, Ann, Talsania, Mitali, Kumar, Jay, Maier-Moore, Jacen S., Harris, Valerie M., Gopalakrishnan, Rajaram, Jonsson, Roland, Lessard, James A., Lu, Xianglan, -Eric Gottenberg, Jacques, -Manuel Anaya, Juan, Cunninghame-Graham, Deborah S., Huang, Andrew J. W., Brennan, Michael T., Hughes, Pamela, Mei, Gabor G., Miceli-Richard, Corinne, Keystone, Edward C., Bykerk, Vivian P., Hirschfield, Gideon, Xie, Gang, Ng, Wan-Fai, Nordmark, Gunnel, Eriksson, Per, Omda, Roald, Rhodus, Nelson L., Rischmueller, Maureen, Rohrer, Michael, Sega, Barbara M., Vvse, Timothy J., Wahren-Herlenius, Marie, Witte, Torsten, Pons-Este, Bernardo, Alarcon-Riquelme, Marta E., Guthridge, Joel M., James, Judith A., Lessard, Christopher J., Kelly, Jennifer A., Thompson, Susan D., Gaffney, Patrick M., Montgomery, Courtney G., Edberg, Jeffrey C., Kimberly, Robert P., Alarcon, Gracicla S., Langefeld, Carl L., Gilkeson, Gary S., Kamen, Diane L., Tsao, Betty P., Joseph McCune, W., Salmon, Jane E., Merrill, Joan T., Weisman, Michael H., Wallace, Daniel J., Utset, Tammy, Bottinger, Erwin P., Amos, Christopher I., Siminovitch, Katherine A., Mariette, Xavier, Sivils, Kathy L., Harley, John B., Hal Scofield, R.
Published in Arthritis & rheumatology (Hoboken, N.J.) (2016)
Published in Arthritis & rheumatology (Hoboken, N.J.) (2016)
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The historical role of species from the Solanaceae plant family in genetic research
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Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders
Hoeffding, Louise K., Duong, Linh T.T., Ingason, Andrés, Rosengren, Anders, Sorbanski, Ester, Witt, Stephanie H., Djurovic, Srdjan, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Rasmussen, Henrik B.
Published in Nordic journal of psychiatry (18.05.2016)
Published in Nordic journal of psychiatry (18.05.2016)
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Abstract 3332: Clonal nuclear and mitochondrial genetic alterations in smoker lung cancer patients and their histologically normal appearing follow-up biopsies
Philley, Julie V., Johnston, Kayla, Banerjee, Hirendra N., Griffith, David E., Dasgupta, Santanu
Published in Cancer research (Chicago, Ill.) (01.07.2019)
Published in Cancer research (Chicago, Ill.) (01.07.2019)
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Identification of Novel Recurrent Copy Number Variations and Regions of Copy-Neutral Loss of Heterozygosity by High Resolution Genomic Array in Pre-Treatment and Relapsed B-CLL
Knight, Samantha JL, Sadighi Akha, Elham, Timbs, Adele, Enver, Tariq, Pettitt, Andrew R, Taylor, Jenny, Hatton, Chris S, Schuh, Anna
Published in Blood (20.11.2009)
Published in Blood (20.11.2009)
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Mutations in VRK1 Associated With Complex Motor and Sensory Axonal Neuropathy Plus Microcephaly
Gonzaga-Jauregui, Claudia, Lotze, Timothy, Jamal, Leila, Penney, Samantha, Campbell, Ian M, Pehlivan, Davut, Hunter, Jill V, W oodbury, Suzanne L, Raymond, Gerald, Adesina, Adekunle M, Jhangiani, Shalini N, Reid, Jeffrey G, Muzny, Donna M, Boerwinkle, Eric, Lupski, James R, Gibbs, Richard A, Wiszniewski, Wojciech
Published in Archives of neurology (Chicago) (01.12.2013)
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Published in Archives of neurology (Chicago) (01.12.2013)
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