Publications:

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Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits.

Psychiatric Genetics

Castellini, Giovanni G; Merola, Giuseppe Pierpaolo GP; Baccaredda, Ottone Boy OB; Pecoraro, Vincenzo V; Bozza, Bernardo B; Cassioli, Emanuele E; Rossi, Eleonora E; Bessi, Valentina V; Sorbi, Sandro S; Nacmias, Benedetta B; Ricca, Valdo V

Publication Date: 2022-12-20

Variant appearance in text: rs6354

PubMed Link: 36729042

Variant Present in the following documents:

• Main text
• pg-33-79.pdf

View BVdb publication page

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs6354

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research

Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K

Publication Date: 2022-11-21

Variant appearance in text: SLC6A4: -185C>A; rs6354

PubMed Link: 36409824

Variant Present in the following documents:

• can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1

View BVdb publication page

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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: rs6354

PubMed Link: 36211978

Variant Present in the following documents:

• Main text
• fnmol-15-925049.pdf

View BVdb publication page

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: rs6354

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM3_ESM.xlsx, sheet 2

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Major Depressive Disorder: Existing Hypotheses about Pathophysiological Mechanisms and New Genetic Findings.

Genes

Kamran, Muhammad M; Bibi, Farhana F; Ur Rehman, Asim A; Morris, Derek W DW

Publication Date: 2022-04-06

Variant appearance in text: rs6354

PubMed Link: 35456452

Variant Present in the following documents:

• Main text
• genes-13-00646.pdf

View BVdb publication page

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Common and Unique Genetic Background between Attention-Deficit/Hyperactivity Disorder and Excessive Body Weight.

Genes

Dmitrzak-Weglarz, Monika M; Paszynska, Elzbieta E; Bilska, Karolina K; Szczesniewska, Paula P; Bryl, Ewa E; Duda, Joanna J; Dutkiewicz, Agata A; Tyszkiewicz-Nwafor, Marta M; Czerski, Piotr P; Hanc, Tomasz T; Slopien, Agnieszka A

Publication Date: 2021-09-13

Variant appearance in text: rs6354

PubMed Link: 34573389

Variant Present in the following documents:

• Main text
• genes-12-01407.pdf

View BVdb publication page

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The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome.

Journal Of Cellular And Molecular Medicine

Mohr, Sandra S; Fritz, Nikola N; Hammer, Christian C; Martínez, Cristina C; Berens, Sabrina S; Schmitteckert, Stefanie S; Wahl, Verena V; Schmidt, Malin M; Houghton, Lesley A LA; Goebel-Stengel, Miriam M; Kabisch, Maria M; Götze, Dorothea D; Milovač, Irina I; D'Amato, Mauro M; Zheng, Tenghao T; Röth, Ralph R; Mönnikes, Hubert H; Engel, Felicitas F; Gauss, Annika A; Tesarz, Jonas J; Raithel, Martin M; Andresen, Viola V; Frieling, Thomas T; Keller, Jutta J; Pehl, Christian C; Stein-Thöringer, Christoph C; Clarke, Gerard G; Kennedy, Paul J PJ; Cryan, John F JF; Dinan, Timothy G TG; Quigley, Eamonn M M EMM; Spiller, Robin R; Beltrán, Caroll C; Madrid, Ana María AM; Torres, Verónica V; Pérez de Arce, Edith E; Herzog, Wolfgang W; Mayer, Emeran A EA; Sayuk, Gregory G; Gazouli, Maria M; Karamanolis, George G; Kapur-Pojskič, Lejla L; Bustamante, Mariona M; Rabionet, Raquel R; Estivil, Xavier X; Franke, André A; Lieb, Wolfgang W; Boeckxstaens, Guy G; Wouters, Mira M MM; Simrén, Magnus M; Rappold, Gudrun A GA; Vicario, Maria M; Santos, Javier J; Schaefert, Rainer R; Lorenzo-Bermejo, Justo J; Niesler, Beate B

Publication Date: 2021-08

Variant appearance in text: rs6354

PubMed Link: 34165249

Variant Present in the following documents:

• Main text
• JCMM-25-8047.pdf

View BVdb publication page

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Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer

Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC

Publication Date: 2021-05-29

Variant appearance in text: SLC6A4: -185C>A; rs6354

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs6354

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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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: rs6354

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: SLC6A4: -185C>A; rs6354

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: SLC6A4: -185C>A; rs6354

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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Serotonin Transporter (5-HTT) Gene Polymorphisms and Susceptibility to Chronic Periodontitis: A Case-Control Study.

Frontiers In Genetics

Wu, Lan L; Deng, Tong T; Wang, Chao-Yang CY; Ren, Xue-Qun XQ; Wang, Yun-Yun YY; Zeng, Xian-Tao XT; Geng, Pei-Liang PL

Publication Date: 2019

Variant appearance in text: rs6354

PubMed Link: 31428137

Variant Present in the following documents:

• Main text
• fgene-10-00706.pdf

View BVdb publication page

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Prenatal Tobacco Exposure Modulated the Association of Genetic variants with Diagnosed ADHD and its symptom domain in children: A Community Based Case-Control Study.

Scientific Reports

Wang, Yanni Y; Hu, Dan D; Chen, Wenjing W; Xue, Hongli H; Du, Yukai Y

Publication Date: 2019-03-12

Variant appearance in text: rs6354

PubMed Link: 30862909

Variant Present in the following documents:

• Main text
• 41598_2019_Article_40850.pdf

View BVdb publication page

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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: SLC6A4: -185C>A; rs6354

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

View BVdb publication page

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs6354

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

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Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression.

Bmc Psychiatry

Lam, Dilys D; Ancelin, Marie-Laure ML; Ritchie, Karen K; Freak-Poli, Rosanne R; Saffery, Richard R; Ryan, Joanne J

Publication Date: 2018-09-04

Variant appearance in text: rs6354

PubMed Link: 30180828

Variant Present in the following documents:

• Main text
• 12888_2018_Article_1850.pdf

View BVdb publication page

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Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort.

Acta Medica Lituanica

Baronas, Karolis K; Rančelis, Tautvydas T; Pranculis, Aidas A; Domarkienė, Ingrida I; Ambrozaitytė, Laima L; Kučinskas, Vaidutis V

Publication Date: 2018

Variant appearance in text: rs6354

PubMed Link: 29928152

Variant Present in the following documents:

• Main text
• aml-25-007.pdf

View BVdb publication page

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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: rs6354

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Association between polymorphisms in the human serotonin transporter gene and lifelong premature ejaculation in the Han population.

Asian Journal Of Andrology

Peng, Dang-Wei DW; Gao, Jing-Jing JJ; Huang, Yuan-Yuan YY; Tang, Dong-Dong DD; Gao, Pan P; Li, Chao C; Liu, Wei-Qun WQ; Dou, Xian-Ming XM; Mao, Jun J; Zhang, Yao Y; Geng, Hao H; Zhang, Xian-Sheng XS

Publication Date: 2018

Variant appearance in text: rs6354

PubMed Link: 28139473

Variant Present in the following documents:

• Main text
• AJA-20-103.pdf

View BVdb publication page

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Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.

Frontiers In Neuroscience

Alexander, John J; Potamianou, Hera H; Xing, Jinchuan J; Deng, Li L; Karagiannidis, Iordanis I; Tsetsos, Fotis F; Drineas, Petros P; Tarnok, Zsanett Z; Rizzo, Renata R; Wolanczyk, Tomasz T; Farkas, Luca L; Nagy, Peter P; Szymanska, Urszula U; Androutsos, Christos C; Tsironi, Vaia V; Koumoula, Anastasia A; Barta, Csaba C; , ; Sandor, Paul P; Barr, Cathy L CL; Tischfield, Jay J; Paschou, Peristera P; Heiman, Gary A GA; Georgitsi, Marianthi M

Publication Date: 2016

Variant appearance in text: rs6354

PubMed Link: 27708560

Variant Present in the following documents:

• DataSheet1.xlsx, sheet 2

View BVdb publication page

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Linking Mitochondria to Synapses: New Insights for Stress-Related Neuropsychiatric Disorders.

Neural Plasticity

Jeanneteau, Freddy F; Arango-Lievano, Margarita M

Publication Date: 2016

Variant appearance in text: rs6354

PubMed Link: 26885402

Variant Present in the following documents:

• Main text
• NP2016-3985063.pdf

View BVdb publication page

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Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports

Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC

Publication Date: 2015-12-08

Variant appearance in text: rs6354

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 1
• mmc3.xlsx, sheet 3
• mmc3.xlsx, sheet 2

View BVdb publication page

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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: rs6354

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

View BVdb publication page

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Validation of candidate anxiety disorder genes using a carbon dioxide challenge task.

Biological Psychology

Savage, Jeanne E JE; McMichael, Omari O; Gorlin, Eugenia I EI; Beadel, Jessica R JR; Teachman, Bethany B; Vladimirov, Vladimir I VI; Hettema, John M JM; Roberson-Nay, Roxann R

Publication Date: 2015-07

Variant appearance in text: rs6354

PubMed Link: 25913301

Variant Present in the following documents:

• Main text

View BVdb publication page

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Direct, indirect and pleiotropic effects of candidate genes on internalizing disorder psychopathology.

Psychological Medicine

Hettema, J M JM; Chen, X X; Sun, C C; Brown, T A TA

Publication Date: 2015-07

Variant appearance in text: rs6354

PubMed Link: 25702797

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association and interaction analyses of 5-HT3 receptor and serotonin transporter genes with alcohol, cocaine, and nicotine dependence using the SAGE data.

Human Genetics

Yang, Jiekun J; Li, Ming D MD

Publication Date: 2014-07

Variant appearance in text: rs6354

PubMed Link: 24590108

Variant Present in the following documents:

• Main text

View BVdb publication page

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Evidence for single nucleotide polymorphisms and their association with bipolar disorder.

Neuropsychiatric Disease And Treatment

Szczepankiewicz, Aleksandra A

Publication Date: 2013

Variant appearance in text: rs6354

PubMed Link: 24143106

Variant Present in the following documents:

• Main text

View BVdb publication page

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Serotonin transporter gene (SLC6A4) variations are associated with poor survival in colorectal cancer patients.

Plos One

Savas, Sevtap S; Hyde, Angela A; Stuckless, Susan N SN; Parfrey, Patrick P; Younghusband, H Banfield HB; Green, Roger R

Publication Date: 2012

Variant appearance in text: rs6354

PubMed Link: 22911682

Variant Present in the following documents:

• Main text
• pone.0038953.pdf

View BVdb publication page

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Examining associations between disordered eating and serotonin transporter gene polymorphisms.

The International Journal Of Eating Disorders

Munn-Chernoff, Melissa A MA; McQueen, Matthew B MB; Stetler, Gary L GL; Haberstick, Brett C BC; Rhee, Soo Hyun SH; Sobik, Laura E LE; Corley, Robin P RP; Smolen, Andrew A; Hewitt, John K JK; Stallings, Michael C MC

Publication Date: 2012-05

Variant appearance in text: rs6354

PubMed Link: 22271047

Variant Present in the following documents:

• Main text

View BVdb publication page

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A genome-wide association study of amygdala activation in youths with and without bipolar disorder.

Journal Of The American Academy Of Child And Adolescent Psychiatry

Liu, Xinmin X; Akula, Nirmala N; Skup, Martha M; Brotman, Melissa A MA; Leibenluft, Ellen E; McMahon, Francis J FJ

Publication Date: 2010-01

Variant appearance in text: rs6354

PubMed Link: 20215924

Variant Present in the following documents:

• Main text

View BVdb publication page

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Serotonin transporter gene, depressive symptoms, and interleukin-6.

Circulation. Cardiovascular Genetics

Su, Shaoyong S; Zhao, Jinying J; Bremner, J Douglas JD; Miller, Andrew H AH; Tang, Weining W; Bouzyk, Mark M; Snieder, Harold H; Novik, Olga O; Afzal, Nadeem N; Goldberg, Jack J; Vaccarino, Viola V

Publication Date: 2009-12

Variant appearance in text: rs6354

PubMed Link: 20031642

Variant Present in the following documents:

• Main text

View BVdb publication page

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Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample.

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

Coventry, William L WL; James, Michael R MR; Eaves, Lindon J LJ; Gordon, Scott D SD; Gillespie, Nathan A NA; Ryan, Leanne L; Heath, Andrew C AC; Montgomery, Grant W GW; Martin, Nicholas G NG; Wray, Naomi R NR

Publication Date: 2010-04-05

Variant appearance in text: rs6354

PubMed Link: 19911410

Variant Present in the following documents:

• Main text

View BVdb publication page

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Pharmacogenetics studies in STAR*D: strengths, limitations, and results.

Psychiatric Services (Washington, D.C.)

Laje, Gonzalo G; Perlis, Roy H RH; Rush, A John AJ; McMahon, Francis J FJ

Publication Date: 2009-11

Variant appearance in text: rs6354

PubMed Link: 19880459

Variant Present in the following documents:

• Main text

View BVdb publication page

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Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures.

Biological Psychiatry

Wray, Naomi R NR; James, Michael R MR; Gordon, Scott D SD; Dumenil, Troy T; Ryan, Leanne L; Coventry, William L WL; Statham, Dixie J DJ; Pergadia, Michele L ML; Madden, Pamela A F PA; Heath, Andrew C AC; Montgomery, Grant W GW; Martin, Nicholas G NG

Publication Date: 2009-09-01

Variant appearance in text: rs6354

PubMed Link: 19541292

Variant Present in the following documents:

• Main text

View BVdb publication page

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Variants of the serotonin transporter gene and NEO-PI-R Neuroticism: No association in the BLSA and SardiNIA samples.

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

Terracciano, Antonio A; Balaci, Lenuta L; Thayer, Jason J; Scally, Matthew M; Kokinos, Sarah S; Ferrucci, Luigi L; Tanaka, Toshiko T; Zonderman, Alan B AB; Sanna, Serena S; Olla, Nazario N; Zuncheddu, Maria Antonietta MA; Naitza, Silvia S; Busonero, Fabio F; Uda, Manuela M; Schlessinger, David D; Abecasis, Gonçalo R GR; Costa, Paul T PT

Publication Date: 2009-12-05

Variant appearance in text: rs6354

PubMed Link: 19199283

Variant Present in the following documents:

• Main text

View BVdb publication page

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Serotonin transporter polymorphisms in patients with portopulmonary hypertension.

Chest

Roberts, Kari E KE; Fallon, Michael B MB; Krowka, Michael J MJ; Benza, Raymond L RL; Knowles, James A JA; Badesch, David B DB; Brown, Robert S RS; Taichman, Darren B DB; Trotter, James J; Zacks, Steven S; Horn, Evelyn M EM; Kawut, Steven M SM; ,

Publication Date: 2009-06

Variant appearance in text: rs6354

PubMed Link: 19141529

Variant Present in the following documents:

• Main text

View BVdb publication page

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Gender moderates the relationship between mania spectrum and serotonin transporter polymorphisms in depression.

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

Rucci, P P; Nimgaonkar, V L VL; Mansour, H H; Miniati, M M; Masala, I I; Fagiolini, A A; Cassano, G B GB; Frank, E E

Publication Date: 2009-10-05

Variant appearance in text: rs6354

PubMed Link: 19125390

Variant Present in the following documents:

• Main text

View BVdb publication page

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Characterization of a functional polymorphism in the 3' UTR of SLC6A4 and its association with drinking intensity.

Alcoholism, Clinical And Experimental Research

Seneviratne, Chamindi C; Huang, Weihua W; Ait-Daoud, Nassima N; Li, Ming D MD; Johnson, Bankole A BA

Publication Date: 2009-02

Variant appearance in text: rs6354

PubMed Link: 19032574

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: rs6354

PubMed Link: 18821566

Variant Present in the following documents:

• Main text

View BVdb publication page

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Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

American Journal Of Human Genetics

Sutcliffe, James S JS; Delahanty, Ryan J RJ; Prasad, Harish C HC; McCauley, Jacob L JL; Han, Qiao Q; Jiang, Lan L; Li, Chun C; Folstein, Susan E SE; Blakely, Randy D RD

Publication Date: 2005-08

Variant appearance in text: rs6354

PubMed Link: 15995945

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women.

Gut

Yeo, A A; Boyd, P P; Lumsden, S S; Saunders, T T; Handley, A A; Stubbins, M M; Knaggs, A A; Asquith, S S; Taylor, I I; Bahari, B B; Crocker, N N; Rallan, R R; Varsani, S S; Montgomery, D D; Alpers, D H DH; Dukes, G E GE; Purvis, I I; Hicks, G A GA

Publication Date: 2004-10

Variant appearance in text: rs6354

PubMed Link: 15361494

Variant Present in the following documents:

• Main text

View BVdb publication page

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