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: rs6275

PubMed Link: 36991000

Variant Present in the following documents:

• 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3

View BVdb publication page

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The Progress and Pitfalls of Pharmacogenetics-Based Precision Medicine in Schizophrenia Spectrum Disorders: A Systematic Review and Meta-Analysis.

Journal Of Personalized Medicine

Teng, Yuxin Y; Sandhu, Amrit A; Liemburg, Edith J EJ; Naderi, Elnaz E; Alizadeh, Behrooz Z BZ

Publication Date: 2023-03-04

Variant appearance in text: rs6275

PubMed Link: 36983653

Variant Present in the following documents:

• Main text
• jpm-13-00471.pdf

View BVdb publication page

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A Phase II Trial of Guadecitabine plus Atezolizumab in Metastatic Urothelial Carcinoma Progressing after Initial Immune Checkpoint Inhibitor Therapy.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research

Jang, H Josh HJ; Hostetter, Galen G; MacFarlane, Alexander W AW; Madaj, Zachary Z; Ross, Eric A EA; Hinoue, Toshinori T; Kulchycki, Justin R JR; Burgos, Ryan S RS; Tafseer, Mahvish M; Alpaugh, R Katherine RK; Schwebel, Candice L CL; Kokate, Rutika R; Geynisman, Daniel M DM; Zibelman, Matthew R MR; Ghatalia, Pooja P; Nichols, Peter W PW; Chung, Woonbok W; Madzo, Jozef J; Hahn, Noah M NM; Quinn, David I DI; Issa, Jean-Pierre J JJ; Topper, Michael J MJ; Baylin, Stephen B SB; Shen, Hui H; Campbell, Kerry S KS; Jones, Peter A PA; Plimack, Elizabeth R ER

Publication Date: 2023-03-16

Variant appearance in text: DRD2: H313H

PubMed Link: 36928921

Variant Present in the following documents:

• ccr-22-3642_supplementary_tables_1_suppts1.xlsx, sheet 3

View BVdb publication page

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Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.

Nature

Mensah, Martin A MA; Niskanen, Henri H; Magalhaes, Alexandre P AP; Basu, Shaon S; Kircher, Martin M; Sczakiel, Henrike L HL; Reiter, Alisa M V AMV; Elsner, Jonas J; Meinecke, Peter P; Biskup, Saskia S; Chung, Brian H Y BHY; Dombrowsky, Gregor G; Eckmann-Scholz, Christel C; Hitz, Marc Phillip MP; Hoischen, Alexander A; Holterhus, Paul-Martin PM; Hülsemann, Wiebke W; Kahrizi, Kimia K; Kalscheuer, Vera M VM; Kan, Anita A; Krumbiegel, Mandy M; Kurth, Ingo I; Leubner, Jonas J; Longardt, Ann Carolin AC; Moritz, Jörg D JD; Najmabadi, Hossein H; Skipalova, Karolina K; Snijders Blok, Lot L; Tzschach, Andreas A; Wiedersberg, Eberhard E; Zenker, Martin M; Garcia-Cabau, Carla C; Buschow, René R; Salvatella, Xavier X; Kraushar, Matthew L ML; Mundlos, Stefan S; Caliebe, Almuth A; Spielmann, Malte M; Horn, Denise D; Hnisz, Denes D

Publication Date: 2023-02-08

Variant appearance in text: DRD2: 939T>C; His313=; rs6275

PubMed Link: 36755093

Variant Present in the following documents:

• 41586_2022_5682_MOESM7_ESM.xlsx, sheet 1

View BVdb publication page

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Pharmacogenetics and Schizophrenia-Can Genomics Improve the Treatment with Second-Generation Antipsychotics?

Biomedicines

Płaza, Olga O; Gałecki, Piotr P; Orzechowska, Agata A; Gałecka, Małgorzata M; Sobolewska-Nowak, Justyna J; Szulc, Agata A

Publication Date: 2022-12-07

Variant appearance in text: rs6275

PubMed Link: 36551925

Variant Present in the following documents:

• Main text
• biomedicines-10-03165.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: DRD2: H313H; rs6275

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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MAOA uVNTR Genetic Variant and Major Depressive Disorder: A Systematic Review.

Cells

Castro Gonçalves, Ana Beatriz AB; Ferreira Fratelli, Caroline C; Saraiva Siqueira, Jhon Willatan JW; Canongia de Abreu Cardoso Duarte, Ligia L; Ribeiro Barros, Aline A; Possatti, Isabella I; Lima Dos Santos, Maurício M; de Souza Silva, Calliandra Maria CM; Rodrigues da Silva, Izabel Cristina IC

Publication Date: 2022-10-17

Variant appearance in text: rs6275

PubMed Link: 36291132

Variant Present in the following documents:

• Main text
• cells-11-03267.pdf

View BVdb publication page

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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: DRD2: H313H

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM2_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM8_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM4_ESM.xlsx, sheet 2

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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: DRD2: H313H; rs6275

PubMed Link: 36075891

Variant Present in the following documents:

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

View BVdb publication page

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Temporomandibular disorder in construction workers associated with ANKK1 and DRD2 genes.

Brazilian Dental Journal

Baratto, Samantha Schaffer Pugsley SSP; Meger, Michelle Nascimento MN; Camargo, Vânia V; Nolasco, Gisele Maria Correr GMC; Mattos, Natanael Henrique Ribeiro NHR; Roskamp, Liliane L; Stechman-Neto, José J; Madalena, Isabela Ribeiro IR; Küchler, Erika Calvano EC; Baratto-Filho, Flares F

Publication Date: 2022

Variant appearance in text: rs6275

PubMed Link: 36043564

Variant Present in the following documents:

• Main text
• 1806-4760-bdj-33-04-12.pdf

View BVdb publication page

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Pathophysiological Mechanisms of Antipsychotic-Induced Parkinsonism.

Biomedicines

Vaiman, Elena E EE; Shnayder, Natalia A NA; Khasanova, Aiperi K AK; Strelnik, Anna I AI; Gayduk, Arseny J AJ; Al-Zamil, Mustafa M; Sapronova, Margarita R MR; Zhukova, Natalia G NG; Smirnova, Daria A DA; Nasyrova, Regina F RF

Publication Date: 2022-08-18

Variant appearance in text: rs6275

PubMed Link: 36009557

Variant Present in the following documents:

• Main text
• biomedicines-10-02010.pdf

View BVdb publication page

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Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics

Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y

Publication Date: 2022

Variant appearance in text: DRD2: 939T>C; His313His; rs6275

PubMed Link: 35899134

Variant Present in the following documents:

• Table_1.xlsx, sheet 1

View BVdb publication page

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Characterization of ADME Gene Variation in Colombian Population by Exome Sequencing.

Frontiers In Pharmacology

Silgado-Guzmán, Daniel Felipe DF; Angulo-Aguado, Mariana M; Morel, Adrien A; Niño-Orrego, María José MJ; Ruiz-Torres, Daniel-Armando DA; Contreras Bravo, Nora Constanza NC; Restrepo, Carlos Martin CM; Ortega-Recalde, Oscar O; Fonseca-Mendoza, Dora Janeth DJ

Publication Date: 2022

Variant appearance in text: DRD2: 939T>C; His313=; rs6275

PubMed Link: 35846994

Variant Present in the following documents:

• Table1.xlsx, sheet 1

View BVdb publication page

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What factors predict craniomandibular disorders in severe COVID-19 survivors after prolonged intubation?

Journal Of Stomatology, Oral And Maxillofacial Surgery

Pitak-Arnnop, Poramate P; Tangmanee, Chatpong C; Mutirangura, Wantanee W; Apipan, Benjamas B; Auychai, Prim P; Meningaud, Jean-Paul JP; Neff, Andreas A

Publication Date: 2022-11

Variant appearance in text: rs6275

PubMed Link: 35809797

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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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: rs6275

PubMed Link: 35768426

Variant Present in the following documents:

• 41531_2022_346_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Influence of COMT (rs4680) and DRD2 (rs1076560, rs1800497) Gene Polymorphisms on Safety and Efficacy of Methylphenidate Treatment in Children with Fetal Alcohol Spectrum Disorders.

International Journal Of Environmental Research And Public Health

Śmiarowska, Małgorzata M; Brzuchalski, Bogusław B; Grzywacz, Elżbieta E; Malinowski, Damian D; Machoy-Mokrzyńska, Anna A; Pierzchlińska, Anna A; Białecka, Monika M

Publication Date: 2022-04-08

Variant appearance in text: rs6275

PubMed Link: 35457347

Variant Present in the following documents:

• Main text
• ijerph-19-04479.pdf

View BVdb publication page

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Genetic overlap between temporomandibular disorders and primary headaches: A systematic review.

The Japanese Dental Science Review

Cruz, Diogo D; Monteiro, Francisca F; Paço, Maria M; Vaz-Silva, Manuel M; Lemos, Carolina C; Alves-Ferreira, Miguel M; Pinho, Teresa T

Publication Date: 2022-11

Variant appearance in text: rs6275

PubMed Link: 35242249

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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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: rs6275

PubMed Link: 35140610

Variant Present in the following documents:

• Main text
• fphar-12-834129.pdf

View BVdb publication page

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Current understanding of the genetics of tourette syndrome.

Biomedical Journal

Lin, Wei-De WD; Tsai, Fuu-Jen FJ; Chou, I-Ching IC

Publication Date: 2022-04

Variant appearance in text: DRD2: H313H; rs6275

PubMed Link: 35042017

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Genetic Markers as Risk Factors for the Development of Impulsive-Compulsive Behaviors in Patients with Parkinson's Disease Receiving Dopaminergic Therapy.

Journal Of Personalized Medicine

Fedosova, Anna A; Titova, Nataliya N; Kokaeva, Zarema Z; Shipilova, Natalia N; Katunina, Elena E; Klimov, Eugene E

Publication Date: 2021-12-07

Variant appearance in text: DRD2: His313His; rs6275

PubMed Link: 34945793

Variant Present in the following documents:

• Main text
• jpm-11-01321.pdf

View BVdb publication page

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Influence of genetic variants of opioid-related genes on opioid-induced adverse effects in patients with lung cancer: A STROBE-compliant observational study.

Medicine

Tanaka, Rei R; Sato, Junya J; Ishikawa, Hiroshi H; Sato, Tetsu T; Shino, Michihiro M; Ohde, Yasuhisa Y; Sato, Tetsumi T; Mori, Keita K; Notsu, Akifumi A; Ohnami, Sumiko S; Mizuguchi, Maki M; Nagashima, Takeshi T; Yamaguchi, Ken K

Publication Date: 2021-11-05

Variant appearance in text: rs6275

PubMed Link: 34871222

Variant Present in the following documents:

• Main text
• medi-100-e27565.pdf

View BVdb publication page

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Preliminary Pharmacogenetic Study to Explore Putative Dopaminergic Mechanisms of Antidepressant Action.

Journal Of Personalized Medicine

Ochi, Taichi T; Vyalova, Natalya M NM; Losenkov, Innokentiy S IS; Paderina, Diana Z DZ; Pozhidaev, Ivan V IV; Loonen, Anton J M AJM; Simutkin, German G GG; Bokhan, Nikolay A NA; Wilffert, Bob B; Ivanova, Svetlana A SA

Publication Date: 2021-07-27

Variant appearance in text: rs6275

PubMed Link: 34442374

Variant Present in the following documents:

• Main text
• jpm-11-00731.pdf

View BVdb publication page

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Candidate Genes Encoding Dopamine Receptors as Predictors of the Risk of Antipsychotic-Induced Parkinsonism and Tardive Dyskinesia in Schizophrenic Patients.

Biomedicines

Vaiman, Elena E EE; Shnayder, Natalia A NA; Novitsky, Maxim A MA; Dobrodeeva, Vera S VS; Goncharova, Polina S PS; Bochanova, Elena N EN; Sapronova, Margarita R MR; Popova, Tatiana E TE; Tappakhov, Alexey A AA; Nasyrova, Regina F RF

Publication Date: 2021-07-23

Variant appearance in text: rs6275

PubMed Link: 34440083

Variant Present in the following documents:

• Main text

View BVdb publication page

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics

Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F

Publication Date: 2021

Variant appearance in text: DRD2: 939T>C; H313H; rs6275

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Polymorphisms of Dopamine Receptor Genes and Parkinson's Disease: Clinical Relevance and Future Perspectives.

International Journal Of Molecular Sciences

Magistrelli, Luca L; Ferrari, Marco M; Furgiuele, Alessia A; Milner, Anna Vera AV; Contaldi, Elena E; Comi, Cristoforo C; Cosentino, Marco M; Marino, Franca F

Publication Date: 2021-04-06

Variant appearance in text: rs6275

PubMed Link: 33917417

Variant Present in the following documents:

• Main text

View BVdb publication page

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Computational Functional Genomics-Based AmpliSeq™ Panel for Next-Generation Sequencing of Key Genes of Pain.

International Journal Of Molecular Sciences

Kringel, Dario D; Malkusch, Sebastian S; Kalso, Eija E; Lötsch, Jörn J

Publication Date: 2021-01-16

Variant appearance in text: rs6275

PubMed Link: 33467215

Variant Present in the following documents:

• Main text
• ijms-22-00878.pdf

View BVdb publication page

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Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.

Saudi Journal Of Biological Sciences

Aboul-Soud, Mourad A M MAM; Alzahrani, Alhussain J AJ; Mahmoud, Amer A

Publication Date: 2021-01

Variant appearance in text: rs6275

PubMed Link: 33424349

Variant Present in the following documents:

• mmc1.xlsx, sheet 1

View BVdb publication page

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Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications

Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A

Publication Date: 2021-01-08

Variant appearance in text: DRD2: 939T>C; H313H; rs6275

PubMed Link: 33420045

Variant Present in the following documents:

• 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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ADORA2A variation and adenosine A1 receptor availability in the human brain with a focus on anxiety-related brain regions: modulation by ADORA1 variation.

Translational Psychiatry

Hohoff, Christa C; Kroll, Tina T; Zhao, Baoyuan B; Kerkenberg, Nicole N; Lang, Ilona I; Schwarte, Kathrin K; Elmenhorst, David D; Elmenhorst, Eva-Maria EM; Aeschbach, Daniel D; Zhang, Weiqi W; Baune, Bernhard T BT; Neumaier, Bernd B; Bauer, Andreas A; Deckert, Jürgen J

Publication Date: 2020-11-24

Variant appearance in text: rs6275

PubMed Link: 33235193

Variant Present in the following documents:

• Main text

View BVdb publication page

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Dopamine D1 Receptor in Cancer.

Cancers

Sobczuk, Paweł P; Łomiak, Michał M; Cudnoch-Jędrzejewska, Agnieszka A

Publication Date: 2020-11-02

Variant appearance in text: rs6275

PubMed Link: 33147760

Variant Present in the following documents:

• Main text
• cancers-12-03232.pdf

View BVdb publication page

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Suicidal ideation and aggression in childhood, genetic variation and young adult depression.

Journal Of Affective Disorders

Hill, Shirley Y SY; Jones, Bobby L BL; Haas, Gretchen L GL

Publication Date: 2020-11-01

Variant appearance in text: rs6275

PubMed Link: 32745832

Variant Present in the following documents:

• Main text

View BVdb publication page

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Pharmacogenomics of methadone: a narrative review of the literature.

Pharmacogenomics

Packiasabapathy, Senthil S; Aruldhas, Blessed W BW; Horn, Nicole N; Overholser, Brian R BR; Quinney, Sara K SK; Renschler, Janelle S JS; Sadhasivam, Senthilkumar S

Publication Date: 2020-08

Variant appearance in text: rs6275

PubMed Link: 32705966

Variant Present in the following documents:

• Main text

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: DRD2: H313H; rs6275

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment.

Molecular Genetics & Genomic Medicine

Paolacci, Stefano S; Kiani, Aysha Karim AK; Manara, Elena E; Beccari, Tommaso T; Ceccarini, Maria Rachele MR; Stuppia, Liborio L; Chiurazzi, Pietro P; Dalla Ragione, Laura L; Bertelli, Matteo M

Publication Date: 2020-07

Variant appearance in text: rs6275

PubMed Link: 32368866

Variant Present in the following documents:

• Main text
• MGG3-8-e1244.pdf

View BVdb publication page

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A new genetic locus for antipsychotic-induced weight gain: A genome-wide study of first-episode psychosis patients using amisulpride (from the OPTiMiSE cohort).

Journal Of Psychopharmacology (Oxford, England)

Ter Hark, Sophie E SE; Jamain, Stéphane S; Schijven, Dick D; Lin, Bochao D BD; Bakker, Mark K MK; Boland-Auge, Anne A; Deleuze, Jean-François JF; Troudet, Réjane R; Malhotra, Anil K AK; Gülöksüz, Sinan S; Vinkers, Christiaan H CH; Ebdrup, Bjørn H BH; Kahn, René S RS; Leboyer, Marion M; Luykx, Jurjen J JJ

Publication Date: 2020-05

Variant appearance in text: rs6275

PubMed Link: 32126890

Variant Present in the following documents:

• Supplementary_Figures_and_Tables_Optimise_GWAS.pdf

View BVdb publication page

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A proposed synergistic effect of CSF1R and NMUR2 variants contributes to binge eating in hereditary diffuse leukoencephalopathy with spheroids.

Annals Of Translational Medicine

Liu, Qing Q; Guo, Xia-Nan XN; Liu, Cai-Yan CY; Xu, Wei-Hai WH

Publication Date: 2020-01

Variant appearance in text: rs6275

PubMed Link: 32055598

Variant Present in the following documents:

• Main text

View BVdb publication page

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Neuropharmacological and Neurogenetic Correlates of Opioid Use Disorder (OUD) As a Function of Ethnicity: Relevance to Precision Addiction Medicine.

Current Neuropharmacology

Abijo, Tomilowo T; Blum, Kenneth K; Gondré-Lewis, Marjorie C MC

Publication Date: 2020

Variant appearance in text: rs6275

PubMed Link: 31744450

Variant Present in the following documents:

• Main text
• CN-18-578.pdf

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: DRD2: 939T>C; His313=; rs6275

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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Molecular Imaging of Opioid and Dopamine Systems: Insights Into the Pharmacogenetics of Opioid Use Disorders.

Frontiers In Psychiatry

Burns, Jamie A JA; Kroll, Danielle S DS; Feldman, Dana E DE; Kure Liu, Christopher C; Manza, Peter P; Wiers, Corinde E CE; Volkow, Nora D ND; Wang, Gene-Jack GJ

Publication Date: 2019

Variant appearance in text: rs6275

PubMed Link: 31620026

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: DRD2: H313H; rs6275

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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Clinical and Genetic Factors Associated with Resistance to Treatment in Patients with Schizophrenia: A Case-Control Study.

International Journal Of Molecular Sciences

Hajj, Aline A; Obeid, Sahar S; Sahyoun, Saria S; Haddad, Chadia C; Azar, Jocelyne J; Rabbaa Khabbaz, Lydia L; Hallit, Souheil S

Publication Date: 2019-09-25

Variant appearance in text: rs6275

PubMed Link: 31557839

Variant Present in the following documents:

• Main text

View BVdb publication page

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