Serotonin transporter 5-HTTLPR genotype moderates the effects of childhood adversity on posttraumatic stress disorder risk: a replication study

od Xie, Pingxing, Kranzler, Henry R., Farrer, Lindsay, Gelernter, Joel
Izdano 2012

Multiple Pairwise Analysis of Non-homologous Centromere Coupling Reveals Preferential Chromosome Size-Dependent Interactions and a Role for Bouquet Formation in Establishing the In...

od Lefrançois, Philippe, Rockmill, Beth, Xie, Pingxing, Roeder, G. Shirleen, Snyder, Michael
Izdano u PLoS Genet (2016)

The transcriptional landscape analysis of basal cell carcinomas reveals novel signalling pathways and actionable targets

od Litvinov, Ivan V, Xie, Pingxing, Gunn, Scott, Sasseville, Denis, Lefrançois, Philippe
Izdano u Life Sci Alliance (2021)

A Complex Interplay between Personality Domains, Marital Status and a Variant in CHRNA5 on the Risks of Cocaine, Nicotine Dependences and Cocaine-Induced Paranoia

od Zayats, Tetyana, Yang, Bao-Zhu, Xie, Pingxing, Poling, James, Farrer, Lindsay A., Gelernter, Joel
Izdano 2013

Genome-wide Association Study Identifies New Susceptibility Loci for Posttraumatic Stress Disorder

od Xie, Pingxing, Kranzler, Henry R., Yang, Can, Zhao, Hongyu, Farrer, Lindsay A., Gelernter, Joel
Izdano 2013

Deep resequencing of 17 glutamate system genes identifies rare variants in DISC1 and GRIN2B affecting risk of opioid dependence

od Xie, Pingxing, Kranzler, Henry R., Krystal, John H., Farrer, Lindsay A., Zhao, Hongyu, Gelernter, Joel
Izdano 2013

In silico analyses of the tumor microenvironment highlight tumoral inflammation, a Th2 cytokine shift and a mesenchymal stem cell-like phenotype in advanced in basal cell carcinoma...

od Lefrançois, Philippe, Xie, Pingxing, Gunn, Scott, Gantchev, Jennifer, Villarreal, Amelia Martínez, Sasseville, Denis, Litvinov, Ivan V.
Izdano u J Cell Commun Signal (2020)

Childhood Adversity Increases Risk for Nicotine Dependence and Interacts with α5 Nicotinic Acetylcholine Receptor Genotype Specifically in Males

od Xie, Pingxing, Kranzler, Henry R, Zhang, Huiping, Oslin, David, Anton, Raymond F, Farrer, Lindsay A, Gelernter, Joel
Izdano 2012

Interaction of FKBP5 with Childhood Adversity on Risk for Post-Traumatic Stress Disorder

od Xie, Pingxing, Kranzler, Henry R, Poling, James, Stein, Murray B, Anton, Raymond F, Farrer, Lindsay A, Gelernter, Joel
Izdano 2010

The Ectopic Expression of Meiosis Regulatory Genes in Cutaneous T-Cell Lymphomas (CTCL)

od Gantchev, Jennifer, Martínez Villarreal, Amelia, Xie, Pingxing, Lefrançois, Philippe, Gunn, Scott, Netchiporouk, Elena, Sasseville, Denis, Litvinov, Ivan V.
Izdano u Front Oncol (2019)

Interactive Effect of Stressful Life Events and the Serotonin Transporter 5-HTTLPR Genotype on Posttraumatic Stress Disorder Diagnosis in 2 Independent Populations

od Xie, Pingxing, Kranzler, Henry R., Poling, James, Stein, Murray B., Anton, Raymond F., Brady, Kathleen, Weiss, Roger D., Farrer, Lindsay, Gelernter, Joel
Izdano 2009

Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility

od Zhang, Feng, Lu, Chuncheng, Li, Zheng, Xie, Pingxing, Xia, Yankai, Zhu, Xiaobin, Wu, Bin, Cai, Xiaoyun, Wang, Xiaofeng, Qian, Ji, Wang, Xinru, Jin, Li
Izdano 2007

Genetic architecture and adaptations of Nunavik Inuit

od Zhou, Sirui, Xie, Pingxing, Quoibion, Amélie, Ambalavanan, Amirthagowri, Dionne-Laporte, Alexandre, Spiegelman, Dan, Bourassa, Cynthia V., Xiong, Lan, Dion, Patrick A., Rouleau, Guy A.
Izdano u Proc Natl Acad Sci U S A (2019)

Rare nonsynonymous variants in alpha-4 nicotinic acetylcholine receptor gene protect against nicotine dependence

od Xie, Pingxing, Kranzler, Henry R., Krauthammer, Michael, Cosgrove, Kelly P., Oslin, David, Anton, Raymond F., Farrer, Lindsay A., Picciotto, Marina R., Krystal, John H., Zhao, Hongyu, Gelernter, Joel
Izdano 2011

Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nunavik Inuit Population

od Zhou, Sirui, Xiong, Lan, Xie, Pingxing, Ambalavanan, Amirthagowri, Bourassa, Cynthia V., Dionne-Laporte, Alexandre, Spiegelman, Dan, Turcotte Gauthier, Maude, Henrion, Edouard, Diallo, Ousmane, Dion, Patrick A., Rouleau, Guy A.
Izdano u PLoS One (2015)

Gene expression profiling and immune cell-type deconvolution highlight robust disease progression and survival markers in multiple cohorts of CTCL patients

od Lefrançois, Philippe, Xie, Pingxing, Wang, Linghua, Tetzlaff, Michael T., Moreau, Linda, Watters, Andrew K., Netchiporouk, Elena, Provost, Nathalie, Gilbert, Martin, Ni, Xiao, Sasseville, Denis, Wheeler, David A., Duvic, Madeleine, Litvinov, Ivan V.
Izdano u Oncoimmunology (2018)

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

od Zhou, Sirui, Gan-Or, Ziv, Ambalavanan, Amirthagowri, Lai, Dongbing, Xie, Pingxing, Bourassa, Cynthia V., Strong, Stephanie, Ross, Jay P., Dionne-Laporte, Alexandre, Spiegelman, Dan, Dupré, Nicolas, Foroud, Tatiana M, Xiong, Lan, Dion, Patrick A., Rouleau, Guy A.
Izdano u Sci Rep (2018)

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

od Zhou, Sirui, Ambalavanan, Amirthagowri, Rochefort, Daniel, Xie, Pingxing, Bourassa, Cynthia V., Hince, Pascale, Dionne-Laporte, Alexandre, Spiegelman, Dan, Gan-Or, Ziv, Mirarchi, Cathy, Zaharieva, Vessela, Dupré, Nicolas, Kobayashi, Hatasu, Hitomi, Toshiaki, Harada, Kouji, Koizumi, Akio, Xiong, Lan, Dion, Patrick A., Rouleau, Guy A.
Izdano u Am J Hum Genet (2016)

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

od Zhu, Xiaolin, Petrovski, Slavé, Xie, Pingxing, Ruzzo, Elizabeth K., Lu, Yi-Fan, McSweeney, K. Melodi, Ben-Zeev, Bruria, Nissenkorn, Andreea, Anikster, Yair, Oz-Levi, Danit, Dhindsa, Ryan S., Hitomi, Yuki, Schoch, Kelly, Spillmann, Rebecca C., Heimer, Gali, Marek-Yagel, Dina, Tzadok, Michal, Han, Yujun, Worley, Gordon, Goldstein, Jennifer, Jiang, Yong-Hui, Lancet, Doron, Pras, Elon, Shashi, Vandana, McHale, Duncan, Need, Anna C., Goldstein, David B.
Izdano u Genet Med (2015)