Publications:

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Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications

Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C

Publication Date: 2023-03-29

Variant appearance in text: N/A

PubMed Link: 36991000

Variant Present in the following documents:

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: HTR1B: S43S

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2

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Attention-deficit/hyperactive disorder updates.

Frontiers In Molecular Neuroscience

Kessi, Miriam M; Duan, Haolin H; Xiong, Juan J; Chen, Baiyu B; He, Fang F; Yang, Lifen L; Ma, Yanli Y; Bamgbade, Olumuyiwa A OA; Peng, Jing J; Yin, Fei F

Publication Date: 2022

Variant appearance in text: rs6298

PubMed Link: 36211978

Variant Present in the following documents:

• Main text
• fnmol-15-925049.pdf

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Integration of Transcriptome and Epigenome to Identify and Develop Prognostic Markers for Ovarian Cancer.

Journal Of Oncology

Xu, Can C; Cao, Wei W

Publication Date: 2022

Variant appearance in text: rs6298

PubMed Link: 36081667

Variant Present in the following documents:

• 3744466.f1.pdf

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Editorial: Role of the serotonergic system in pathology of major depressive disorders.

Frontiers In Psychiatry

Norman, Trevor Ronald TR

Publication Date: 2022

Variant appearance in text: rs6298

PubMed Link: 36003982

Variant Present in the following documents:

• Main text
• fpsyt-13-988307.pdf

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Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease

Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD

Publication Date: 2022-06-29

Variant appearance in text: N/A

PubMed Link: 35768426

Variant Present in the following documents:

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Genetic Factors Associated With Tardive Dyskinesia: From Pre-clinical Models to Clinical Studies.

Frontiers In Pharmacology

Tsermpini, Evangelia Eirini EE; Redenšek, Sara S; Dolžan, Vita V

Publication Date: 2021

Variant appearance in text: rs6298

PubMed Link: 35140610

Variant Present in the following documents:

• Main text
• fphar-12-834129.pdf

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Neoadjuvant PD-1 Blockade Combined With Chemotherapy Followed by Concurrent Immunoradiotherapy in Locally Advanced Anal Canal Squamous Cell Carcinoma Patients: Antitumor Efficacy, Safety and Biomarker Analysis.

Frontiers In Immunology

Xiao, WeiWei W; Yuan, Yan Y; Wang, SuiHai S; Liao, Zhidong Z; Cai, PeiQiang P; Chen, BaoQing B; Zhang, Rong R; Wang, Fang F; Zeng, ZhiFan Z; Gao, YuanHong Y

Publication Date: 2021

Variant appearance in text: HTR1B: S43S

PubMed Link: 35095878

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

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Obsessive-Compulsive Disorder Interactome Profile Analysis: A Perspective From Molecular Mechanism.

Basic And Clinical Neuroscience

Zamanian-Azodi, Mona M; Rezaei-Tavirani, Mostafa M; Rezaei Tavirani, Majid M

Publication Date: 2021

Variant appearance in text: rs6298

PubMed Link: 34925715

Variant Present in the following documents:

• Main text
• BCN-12-187.pdf

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A Meta-Analysis of 5-Hydroxytryptamine Receptor 1B Polymorphisms With Risk of Major Depressive Disorder and Suicidal Behavior.

Frontiers In Psychiatry

Yang, Pingliang P; Yang, Mengchang M; Li, Peng P; Cao, Dejun D; Gong, Daoyin D; Lv, Jiahua J; Pu, Linmei L; Huang, Sizhou S; Liang, Yundan Y

Publication Date: 2021

Variant appearance in text: rs6298

PubMed Link: 34322042

Variant Present in the following documents:

• Main text
• fpsyt-12-696655.pdf

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Genetic Susceptibility to Drug Teratogenicity: A Systematic Literature Review.

Frontiers In Genetics

Gomes, Julia do Amaral JDA; Olstad, Emilie Willoch EW; Kowalski, Thayne Woycinck TW; Gervin, Kristina K; Vianna, Fernanda Sales Luiz FSL; Schüler-Faccini, Lavínia L; Nordeng, Hedvig Marie Egeland HME

Publication Date: 2021

Variant appearance in text: rs6298

PubMed Link: 33981330

Variant Present in the following documents:

• Main text

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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology

Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA

Publication Date: 2021

Variant appearance in text: N/A

PubMed Link: 33791233

Variant Present in the following documents:

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Functional polymorphisms and transcriptional analysis in the 5' region of the human serotonin receptor 1B gene (HTR1B) and their associations with psychiatric disorders.

Bmc Psychiatry

Xia, Xi X; Ding, Mei M; Xuan, Jin-Feng JF; Xing, Jia-Xin JX; Yao, Jun J; Wu, Xue X; Wang, Bao-Jie BJ

Publication Date: 2020-10-09

Variant appearance in text: rs6298

PubMed Link: 33036580

Variant Present in the following documents:

• Main text
• 12888_2020_Article_2906.pdf

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Effects of HTR1B 3' region polymorphisms and functional regions on gene expression regulation.

Bmc Genetics

Xia, Xi X; Ding, Mei M; Xuan, Jin-Feng JF; Xing, Jia-Xin JX; Pang, Hao H; Yao, Jun J; Wu, Xue X; Wang, Bao-Jie BJ

Publication Date: 2020-07-20

Variant appearance in text: rs6298

PubMed Link: 32689951

Variant Present in the following documents:

• Main text
• 12863_2020_Article_886.pdf

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Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis

Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q

Publication Date: 2020-09

Variant appearance in text: N/A

PubMed Link: 32529721

Variant Present in the following documents:

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5-Hydroxytryptamine Receptors and Tardive Dyskinesia in Schizophrenia.

Frontiers In Molecular Neuroscience

Pozhidaev, Ivan V IV; Paderina, Diana Z DZ; Fedorenko, Olga Yu OY; Kornetova, Elena G EG; Semke, Arkadiy V AV; Loonen, Anton J M AJM; Bokhan, Nikolay A NA; Wilffert, Bob B; Ivanova, Svetlana A SA

Publication Date: 2020

Variant appearance in text: rs6298

PubMed Link: 32390801

Variant Present in the following documents:

• Main text

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Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.

Communications Biology

Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF

Publication Date: 2020-04-20

Variant appearance in text: rs6298

PubMed Link: 32313182

Variant Present in the following documents:

• 42003_2020_885_MOESM2_ESM.xlsx, sheet 1

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Machine learning classification of ADHD and HC by multimodal serotonergic data.

Translational Psychiatry

Kautzky, A A; Vanicek, T T; Philippe, C C; Kranz, G S GS; Wadsak, W W; Mitterhauser, M M; Hartmann, A A; Hahn, A A; Hacker, M M; Rujescu, D D; Kasper, S S; Lanzenberger, R R

Publication Date: 2020-04-07

Variant appearance in text: rs6298

PubMed Link: 32265436

Variant Present in the following documents:

• Main text
• 41398_2020_Article_781.pdf

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A pan-cancer analysis of synonymous mutations.

Nature Communications

Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S

Publication Date: 2019-06-12

Variant appearance in text: HTR1B: 129C>T

PubMed Link: 31189880

Variant Present in the following documents:

• 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1

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Systems Approach to Identify Common Genes and Pathways Associated with Response to Selective Serotonin Reuptake Inhibitors and Major Depression Risk.

International Journal Of Molecular Sciences

Srivastava, Ankit A; Singh, Priyanka P; Gupta, Hitesh H; Kaur, Harpreet H; Kanojia, Neha N; Guin, Debleena D; Sood, Mamta M; Chadda, Rakesh Kumar RK; Yadav, Jyoti J; Vohora, Divya D; Saso, Luciano L; Kukreti, Ritushree R

Publication Date: 2019-04-23

Variant appearance in text: rs6298

PubMed Link: 31018568

Variant Present in the following documents:

• Main text
• ijms-20-01993.pdf

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Association of Monoamine Oxidase A (MAOA) Gene uVNTR and rs6323 Polymorphisms with Attention Deficit and Hyperactivity Disorder in Korean Children.

Medicina (Kaunas, Lithuania)

Hwang, In Wook IW; Lim, Myung Ho MH; Kwon, Ho Jang HJ; Jin, Han Jun HJ

Publication Date: 2018-05-18

Variant appearance in text: rs6298

PubMed Link: 30344263

Variant Present in the following documents:

• Main text
• medicina-54-00032.pdf

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: HTR1B: 129C>T; rs6298

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1
• Table_7.xlsx, sheet 1

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Genetic Correlates of Spirituality/Religion and Depression: A Study in Offspring and Grandchildren at High and Low Familial Risk for Depression.

Spirituality In Clinical Practice (Washington, D.C.)

Anderson, Micheline R MR; Miller, Lisa L; Wickramaratne, Priya P; Svob, Connie C; Odgerel, Zagaa Z; Zhao, Ruixin R; Weissman, Myrna M MM

Publication Date: 2017-03

Variant appearance in text: rs6298

PubMed Link: 29057276

Variant Present in the following documents:

• Main text

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs6298

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

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TPH-2 Polymorphisms Interact with Early Life Stress to Influence Response to Treatment with Antidepressant Drugs.

The International Journal Of Neuropsychopharmacology

Xu, Zhi Z; Reynolds, Gavin P GP; Yuan, Yonggui Y; Shi, Yanyan Y; Pu, Mengjia M; Zhang, Zhijun Z

Publication Date: 2016-11

Variant appearance in text: rs6298

PubMed Link: 27521242

Variant Present in the following documents:

• Main text
• pyw070.pdf

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5-HT2A Gene Variants Moderate the Association between PTSD and Reduced Default Mode Network Connectivity.

Frontiers In Neuroscience

Miller, Mark W MW; Sperbeck, Emily E; Robinson, Meghan E ME; Sadeh, Naomi N; Wolf, Erika J EJ; Hayes, Jasmeet P JP; Logue, Mark M; Schichman, Steven A SA; Stone, Angie A; Milberg, William W; McGlinchey, Regina R

Publication Date: 2016

Variant appearance in text: rs6298

PubMed Link: 27445670

Variant Present in the following documents:

• Main text
• fnins-10-00299.pdf

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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget

Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S

Publication Date: 2015-06-20

Variant appearance in text: N/A

PubMed Link: 25944692

Variant Present in the following documents:

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Whole exome sequencing of a single osteosarcoma case--integrative analysis with whole transcriptome RNA-seq data.

Human Genomics

Reimann, Ene E; Kõks, Sulev S; Ho, Xuan Dung XD; Maasalu, Katre K; Märtson, Aare A

Publication Date: 2014-12-11

Variant appearance in text: N/A

PubMed Link: 25496518

Variant Present in the following documents:

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Whole-genome sequencing of the world's oldest people.

Plos One

Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK

Publication Date: 2014

Variant appearance in text: N/A

PubMed Link: 25390934

Variant Present in the following documents:

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Pharmacogenomics in psychiatry: the relevance of receptor and transporter polymorphisms.

British Journal Of Clinical Pharmacology

Reynolds, Gavin P GP; McGowan, Olga O OO; Dalton, Caroline F CF

Publication Date: 2014-04

Variant appearance in text: rs6298

PubMed Link: 24354796

Variant Present in the following documents:

• Main text

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Associations of the 5-hydroxytryptamine (serotonin) receptor 1B gene (HTR1B) with alcohol, cocaine, and heroin abuse.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Cao, Jian J; LaRocque, Emily E; Li, Dawei D

Publication Date: 2013-03

Variant appearance in text: rs6298

PubMed Link: 23335468

Variant Present in the following documents:

• Main text

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The role of the serotonergic system at the interface of aggression and suicide.

Neuroscience

Bortolato, M M; Pivac, N N; Muck Seler, D D; Nikolac Perkovic, M M; Pessia, M M; Di Giovanni, G G

Publication Date: 2013-04-16

Variant appearance in text: N/A

PubMed Link: 23333677

Variant Present in the following documents:

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Polymorphisms of the serotonin transporter and receptor genes: susceptibility to substance abuse.

Substance Abuse And Rehabilitation

Herman, Aryeh I AI; Balogh, Kornelia N KN

Publication Date: 2012-06

Variant appearance in text: rs6298

PubMed Link: 22933845

Variant Present in the following documents:

• Main text
• sar-3-049.pdf

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Search for genetic markers and functional variants involved in the development of opiate and cocaine addiction and treatment.

Annals Of The New York Academy Of Sciences

Yuferov, Vadim V; Levran, Orna O; Proudnikov, Dmitri D; Nielsen, David A DA; Kreek, Mary Jeanne MJ

Publication Date: 2010-02

Variant appearance in text: rs6298

PubMed Link: 20201854

Variant Present in the following documents:

• Main text

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SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE

Publication Date: 2008-12-05

Variant appearance in text: rs6298

PubMed Link: 18821566

Variant Present in the following documents:

• Main text

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