Publications:

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Incorporating multi-stage diagnosis status to mine associations between genetic risk variants and the multi-modality phenotype network in major depressive disorder.

Frontiers In Psychiatry

Zhang, Li L; Pang, Mengqian M; Liu, Xiaoyun X; Hao, Xiaoke X; Wang, Meiling M; Xie, Chunming C; Zhang, Zhijun Z; Yuan, Yonggui Y; Zhang, Daoqiang D

Publication Date: 2023

Variant appearance in text: rs1799913

PubMed Link: 36937715

Variant Present in the following documents:

• Main text
• fpsyt-14-1139451.pdf

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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: rs1799913

PubMed Link: 36075891

Variant Present in the following documents:

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

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Association between TPH1 polymorphisms and the risk of suicide behavior: An updated meta-analysis of 18,398 individuals.

Frontiers In Psychiatry

Genis-Mendoza, Alma Delia AD; Hernández-Díaz, Yazmín Y; González-Castro, Thelma Beatriz TB; Tovilla-Zárate, Carlos Alfonso CA; Castillo-Avila, Rosa Giannina RG; López-Narváez, María Lilia ML; Ramos-Méndez, Miguel Ángel MÁ; Nicolini, Humberto H

Publication Date: 2022

Variant appearance in text: rs1799913

PubMed Link: 35928776

Variant Present in the following documents:

• Main text
• fpsyt-13-932135.pdf

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Relationships of Ischemic Stroke Occurrence and Outcome with Gene Variants Encoding Enzymes of Tryptophan Metabolism.

Biomedicines

Boros, Fanni Annamária FA; Maszlag-Török, Rita R; Szűcs, Mónika M; Annus, Ádám Á; Klivényi, Péter P; Vécsei, László L

Publication Date: 2021-10-11

Variant appearance in text: rs1799913

PubMed Link: 34680558

Variant Present in the following documents:

• Main text
• biomedicines-09-01441.pdf

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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: TPH1: 804-7C>A; rs1799913

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

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LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.

Plos Genetics

Goldstein, Jeffery A JA; Weinstock, Joshua S JS; Bastarache, Lisa A LA; Larach, Daniel B DB; Fritsche, Lars G LG; Schmidt, Ellen M EM; Brummett, Chad M CM; Kheterpal, Sachin S; Abecasis, Goncalo R GR; Denny, Joshua C JC; Zawistowski, Matthew M

Publication Date: 2020-11

Variant appearance in text: rs1799913

PubMed Link: 33175840

Variant Present in the following documents:

• Main text
• pgen.1009077.pdf

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Paternal indifference and neglect in early life and creativity: Exploring the moderating role of TPH1 genotype and offspring gender.

Plos One

Yu, Qi Q; Si, Si S; Zhang, Shun S; Zhang, Jinghuan J

Publication Date: 2020

Variant appearance in text: rs1799913

PubMed Link: 32726303

Variant Present in the following documents:

• Main text
• pone.0221383.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: rs1799913

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

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Pharmacogenomic Characterization in Bipolar Spectrum Disorders.

Pharmaceutics

Fortinguerra, Stefano S; Sorrenti, Vincenzo V; Giusti, Pietro P; Zusso, Morena M; Buriani, Alessandro A

Publication Date: 2019-12-21

Variant appearance in text: rs1799913

PubMed Link: 31877761

Variant Present in the following documents:

• Main text

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Variation of Genes Encoding Tryptophan Catabolites Pathway Enzymes in Stroke.

Journal Of Clinical Medicine

Wigner, Paulina P; Saluk-Bijak, Joanna J; Synowiec, Ewelina E; Miller, Elzbieta E; Sliwinski, Tomasz T; Cichon, Natalia N; Bijak, Michal M

Publication Date: 2019-12-03

Variant appearance in text: TPH1: 804-7C>A; rs1799913

PubMed Link: 31817010

Variant Present in the following documents:

• Main text
• jcm-08-02133-s001.pdf
• jcm-08-02133.pdf

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: rs1799913

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1

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Horizontal and vertical integrative analysis methods for mental disorders omics data.

Scientific Reports

Wang, Shuaichao S; Shi, Xingjie X; Wu, Mengyun M; Ma, Shuangge S

Publication Date: 2019-09-17

Variant appearance in text: rs1799913

PubMed Link: 31530853

Variant Present in the following documents:

• Main text
• 41598_2019_Article_49718.pdf

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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease

Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D

Publication Date: 2019-02-27

Variant appearance in text: TPH1: 804-7C>A; rs1799913

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3

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Gray Matter Volume Reductions Were Associated with TPH1 Polymorphisms in Depressive Disorder Patients with Suicidal Attempts.

Psychiatry Investigation

Lee, Sang Min SM; Lee, Soyoen S; Kang, Won Sub WS; Jahng, Geon-Ho GH; Park, Hae Jeong HJ; Kim, Su Kang SK; Park, Jin Kyung JK

Publication Date: 2018-12

Variant appearance in text: rs1799913

PubMed Link: 30602107

Variant Present in the following documents:

• Main text

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The Interaction of TPH1 A779C Polymorphism and Maternal Authoritarianism on Creative Potential.

Frontiers In Psychology

Zhang, Jinghuan J; Han, Xiao X; Si, Si S; Zhang, Shun S

Publication Date: 2018

Variant appearance in text: rs1799913

PubMed Link: 30450068

Variant Present in the following documents:

• Main text
• fpsyg-09-02106.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: TPH1: 804-7C>A; rs1799913

PubMed Link: 30319441

Variant Present in the following documents:

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

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Genetic, Psychological, and Personal Network Factors Associated With Changes in Binge Drinking Over 2 Years Among Mexican Heritage Adolescents in the USA.

Annals Of Behavioral Medicine : A Publication Of The Society Of Behavioral Medicine

Song, Sunmi S; Marcum, Christopher Steven CS; Wilkinson, Anna V AV; Shete, Sanjay S; Koehly, Laura M LM

Publication Date: 2019-02-01

Variant appearance in text: rs1799913

PubMed Link: 29697747

Variant Present in the following documents:

• Main text

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Association between single nucleotide polymorphisms of TPH1 and TPH2 genes, and depressive disorders.

Journal Of Cellular And Molecular Medicine

Wigner, Paulina P; Czarny, Piotr P; Synowiec, Ewelina E; Bijak, Michał M; Białek, Katarzyna K; Talarowska, Monika M; Galecki, Piotr P; Szemraj, Janusz J; Sliwinski, Tomasz T

Publication Date: 2018-03

Variant appearance in text: TPH1: 804-7C>A; rs1799913

PubMed Link: 29314569

Variant Present in the following documents:

• Main text
• JCMM-22-1778.pdf

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Neural and psychological characteristics of college students with alcoholic parents differ depending on current alcohol use.

Progress In Neuro-Psychopharmacology & Biological Psychiatry

Brown-Rice, Kathleen A KA; Scholl, Jamie L JL; Fercho, Kelene A KA; Pearson, Kami K; Kallsen, Noah A NA; Davies, Gareth E GE; Ehli, Erik A EA; Olson, Seth S; Schweinle, Amy A; Baugh, Lee A LA; Forster, Gina L GL

Publication Date: 2018-02-02

Variant appearance in text: rs1799913

PubMed Link: 28939188

Variant Present in the following documents:

• Main text

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Genetic moderation of cocaine subjective effects by variation in the TPH1, TPH2, and SLC6A4 serotonin genes.

Psychiatric Genetics

Patriquin, Michelle A MA; Hamon, Sara C SC; Harding, Mark J MJ; Nielsen, Ellen M EM; Newton, Thomas F TF; De La Garza, Richard R; Nielsen, David A DA

Publication Date: 2017-10

Variant appearance in text: rs1799913

PubMed Link: 28590957

Variant Present in the following documents:

• Main text

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The Life Span Model of Suicide and Its Neurobiological Foundation.

Frontiers In Neuroscience

Ludwig, Birgit B; Roy, Bhaskar B; Wang, Qingzhong Q; Birur, Badari B; Dwivedi, Yogesh Y

Publication Date: 2017

Variant appearance in text: rs1799913

PubMed Link: 28261051

Variant Present in the following documents:

• Main text

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Genetic Consideration of Schizotypal Traits: A Review.

Frontiers In Psychology

Walter, Emma E EE; Fernandez, Francesca F; Snelling, Mollie M; Barkus, Emma E

Publication Date: 2016

Variant appearance in text: rs1799913

PubMed Link: 27895608

Variant Present in the following documents:

• Main text
• fpsyg-07-01769.pdf

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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: rs1799913

PubMed Link: 27521242

Variant Present in the following documents:

• Main text
• pyw070.pdf

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Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Molecular Psychiatry

Bonvicini, C C; Faraone, S V SV; Scassellati, C C

Publication Date: 2016-07

Variant appearance in text: rs1799913

PubMed Link: 27217152

Variant Present in the following documents:

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Integrative Bayesian analysis of neuroimaging-genetic data with application to cocaine dependence.

Neuroimage

Azadeh, Shabnam S; Hobbs, Brian P BP; Ma, Liangsuo L; Nielsen, David A DA; Gerard Moeller, F F; Baladandayuthapani, Veerabhadran V

Publication Date: 2016-01-15

Variant appearance in text: rs1799913

PubMed Link: 26484829

Variant Present in the following documents:

• Main text

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Susceptibility loci for heroin and cocaine addiction in the serotonergic and adrenergic pathways in populations of different ancestry.

Pharmacogenomics

Levran, Orna O; Peles, Einat E; Randesi, Matthew M; Correa da Rosa, Joel J; Ott, Jurg J; Rotrosen, John J; Adelson, Miriam M; Kreek, Mary Jeanne MJ

Publication Date: 2015

Variant appearance in text: rs1799913

PubMed Link: 26227246

Variant Present in the following documents:

• Main text

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Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease.

Bmc Neurology

Yokoyama, Jennifer S JS; Bonham, Luke W LW; Sears, Renee L RL; Klein, Eric E; Karydas, Anna A; Kramer, Joel H JH; Miller, Bruce L BL; Coppola, Giovanni G

Publication Date: 2015-03-28

Variant appearance in text: rs1799913

PubMed Link: 25880661

Variant Present in the following documents:

• Main text
• 12883_2015_Article_304.pdf

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Dopamine and serotonin genetic risk scores predicting substance and nicotine use in attention deficit/hyperactivity disorder.

Addiction Biology

Groenman, Annabeth P AP; Greven, Corina U CU; van Donkelaar, Marjolein M J MM; Schellekens, Arnt A; van Hulzen, Kimm J E KJ; Rommelse, Nanda N; Hartman, Catharina A CA; Hoekstra, Pieter J PJ; Luman, Marjolein M; Franke, Barbara B; Faraone, Stephen V SV; Oosterlaan, Jaap J; Buitelaar, Jan K JK

Publication Date: 2016-07

Variant appearance in text: rs1799913

PubMed Link: 25752199

Variant Present in the following documents:

• Main text

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Pilot study of Biomarkers for predicting effectiveness of ramosetron in diarrhea-predominant irritable bowel syndrome: expression of S100A10 and polymorphisms of TPH1.

Neurogastroenterology And Motility : The Official Journal Of The European Gastrointestinal Motility Society

Shiotani, A A; Kusunoki, H H; Ishii, M M; Imamura, H H; Manabe, N N; Kamada, T T; Hata, J J; Merchant, J L JL; Haruma, K K

Publication Date: 2015-01

Variant appearance in text: rs1799913

PubMed Link: 25428414

Variant Present in the following documents:

• Main text

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Polymorphisms in genes implicated in dopamine, serotonin and noradrenalin metabolism suggest association with cerebrospinal fluid monoamine metabolite concentrations in psychosis.

Behavioral And Brain Functions : Bbf

Andreou, Dimitrios D; Söderman, Erik E; Axelsson, Tomas T; Sedvall, Göran C GC; Terenius, Lars L; Agartz, Ingrid I; Jönsson, Erik G EG

Publication Date: 2014-07-29

Variant appearance in text: rs1799913

PubMed Link: 25073638

Variant Present in the following documents:

• Main text

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Association of TPH-1 and TPH-2 gene polymorphisms with suicidal behavior: a systematic review and meta-analysis.

Bmc Psychiatry

González-Castro, Thelma Beatriz TB; Juárez-Rojop, Isela I; López-Narváez, María Lilia ML; Tovilla-Zárate, Carlos Alfonso CA

Publication Date: 2014-07-08

Variant appearance in text: rs1799913

PubMed Link: 25005534

Variant Present in the following documents:

• Main text
• 1471-244X-14-196.pdf

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TPH1 A218C polymorphism and temperament in major depression.

Bmc Psychiatry

Andre, Kadri K; Kampman, Olli O; Viikki, Merja M; Illi, Ari A; Setälä-Soikkeli, Eija E; Poutanen, Outi O; Mononen, Nina N; Leinonen, Esa E; Lehtimäki, Terho T

Publication Date: 2013-04-18

Variant appearance in text: rs1799913

PubMed Link: 23597148

Variant Present in the following documents:

• Main text

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The association of attempted suicide with genetic variants in the SLC6A4 and TPH genes depends on the definition of suicidal behavior: a systematic review and meta-analysis.

Translational Psychiatry

Clayden, R C RC; Zaruk, A A; Meyre, D D; Thabane, L L; Samaan, Z Z

Publication Date: 2012-10-02

Variant appearance in text: rs1799913

PubMed Link: 23032942

Variant Present in the following documents:

• Main text
• tp201296a.pdf

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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: rs1799913

PubMed Link: 22933845

Variant Present in the following documents:

• Main text

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The effects of child maltreatment on early signs of antisocial behavior: genetic moderation by tryptophan hydroxylase, serotonin transporter, and monoamine oxidase A genes.

Development And Psychopathology

Cicchetti, Dante D; Rogosch, Fred A FA; Thibodeau, Eric L EL

Publication Date: 2012-08

Variant appearance in text: rs1799913

PubMed Link: 22781862

Variant Present in the following documents:

• Main text

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Paradox of schizophrenia genetics: is a paradigm shift occurring?

Behavioral And Brain Functions : Bbf

Doi, Nagafumi N; Hoshi, Yoko Y; Itokawa, Masanari M; Yoshikawa, Takeo T; Ichikawa, Tomoe T; Arai, Makoto M; Usui, Chie C; Tachikawa, Hirokazu H

Publication Date: 2012-05-31

Variant appearance in text: rs1799913

PubMed Link: 22650965

Variant Present in the following documents:

• Main text

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Risk and protective genetic variants in suicidal behaviour: association with SLC1A2, SLC1A3, 5-HTR1B &NTRK2 polymorphisms.

Behavioral And Brain Functions : Bbf

Murphy, Therese M TM; Ryan, Maria M; Foster, Tom T; Kelly, Chris C; McClelland, Roy R; O'Grady, John J; Corcoran, Eleanor E; Brady, John J; Reilly, Michael M; Jeffers, Anne A; Brown, Katherine K; Maher, Anne A; Bannan, Noreen N; Casement, Alison A; Lynch, Dermot D; Bolger, Sharon S; Tewari, Prerna P; Buckley, Avril A; Quinlivan, Leah L; Daly, Leslie L; Kelleher, Cecily C; Malone, Kevin M KM

Publication Date: 2011-06-28

Variant appearance in text: rs1799913

PubMed Link: 21711518

Variant Present in the following documents:

• Main text
• 1744-9081-7-22.pdf

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The role of genetics in IBS.

Gastroenterology Clinics Of North America

Saito, Yuri A YA

Publication Date: 2011-03

Variant appearance in text: rs1799913

PubMed Link: 21333900

Variant Present in the following documents:

• Main text

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Associations of tryptophan hydroxylase gene polymorphisms with irritable bowel syndrome.

Neurogastroenterology And Motility : The Official Journal Of The European Gastrointestinal Motility Society

Jun, S S; Kohen, R R; Cain, K C KC; Jarrett, M E ME; Heitkemper, M M MM

Publication Date: 2011-03

Variant appearance in text: rs1799913

PubMed Link: 21073637

Variant Present in the following documents:

• Main text

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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: rs1799913

PubMed Link: 20201854

Variant Present in the following documents:

• Main text

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The tryptophan hydroxylase-1 A218C polymorphism is associated with diagnosis, but not suicidal behavior, in borderline personality disorder.

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

Wilson, Scott T ST; Stanley, Barbara B; Brent, David A DA; Oquendo, Maria A MA; Huang, Yung-yu YY; Mann, J John JJ

Publication Date: 2009-03-05

Variant appearance in text: rs1799913

PubMed Link: 18506706

Variant Present in the following documents:

• Main text

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Association between 5-HT2A, TPH1 and GNB3 genotypes and response to typical neuroleptics: a serotonergic approach.

Bmc Psychiatry

Anttila, Sami S; Kampman, Olli O; Illi, Ari A; Rontu, Riikka R; Lehtimäki, Terho T; Leinonen, Esa E

Publication Date: 2007-05-23

Variant appearance in text: rs1799913

PubMed Link: 17521439

Variant Present in the following documents:

• Main text
• 1471-244X-7-22.pdf

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Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology

Cross, Sarah S; Kim, Soo-Jeong SJ; Weiss, Lauren A LA; Delahanty, Ryan J RJ; Sutcliffe, James S JS; Leventhal, Bennett L BL; Cook, Edwin H EH; Veenstra-Vanderweele, Jeremy J

Publication Date: 2008-01

Variant appearance in text: rs1799913

PubMed Link: 17406648

Variant Present in the following documents:

• Main text

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