Publications:

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Non-coding RNA regulation of integrins and their potential as therapeutic targets in cancer.

Cellular Oncology (Dordrecht)

Verhoeff, Tristan Joseph TJ; Holloway, Adele F AF; Dickinson, Joanne L JL

Publication Date: 2022-12-13

Variant appearance in text: rs3809865

PubMed Link: 36512308

Variant Present in the following documents:

• Main text
• 13402_2022_Article_752.pdf

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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: rs3809865

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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: rs3809865

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2

View BVdb publication page

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The association between two genetic polymorphisms in ITGB3 and increase risk of venous thromboembolism in cancer patients in Eastern Province of Saudi Arabia.

Saudi Journal Of Biological Sciences

Alsulaim, Asma Y AY; Azam, Faisal F; Sebastian, Tunny T; Mahdi Hassan, Fathelrahman F; AbdulAzeez, Sayed S; Borgio, J Francis JF; Alzahrani, Faisal M FM

Publication Date: 2022-01

Variant appearance in text: rs3809865

PubMed Link: 35002407

Variant Present in the following documents:

• Main text
• main.pdf

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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: rs3809865

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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Citalopram-induced pathways regulation and tentative treatment-outcome-predicting biomarkers in lymphoblastoid cell lines from depression patients.

Translational Psychiatry

Barakat, Abdul Karim AK; Scholl, Catharina C; Steffens, Michael M; Brandenburg, Kerstin K; Ising, Marcus M; Lucae, Susanne S; Holsboer, Florian F; Laje, Gonzalo G; Kalayda, Ganna V GV; Jaehde, Ulrich U; Stingl, Julia Carolin JC

Publication Date: 2020-07-01

Variant appearance in text: rs3809865

PubMed Link: 32612257

Variant Present in the following documents:

• Main text
• 41398_2020_Article_900.pdf

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: rs3809865

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: rs3809865

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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Association between MBL2 haplotypes and dengue severity in children from Rio de Janeiro, Brazil.

Memorias Do Instituto Oswaldo Cruz

Ornelas, Alice Maria de Magalhães AMM; Xavier-de-Carvalho, Caroline C; Alvarado-Arnez, Lucia Elena LE; Ribeiro-Alves, Marcelo M; Rossi, Átila Duque ÁD; Tanuri, Amilcar A; de Aguiar, Renato Santana RS; Moraes, Milton Ozório MO; Cardoso, Cynthia Chester CC

Publication Date: 2019

Variant appearance in text: rs3809865

PubMed Link: 31141020

Variant Present in the following documents:

• Main text
• 1678-8060-mioc-114-e190004.pdf

View BVdb publication page

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Cancer-associated thrombosis: The search for the holy grail continues.

Research And Practice In Thrombosis And Haemostasis

Ünlü, Betül B; Versteeg, Henri H HH

Publication Date: 2018-10

Variant appearance in text: rs3809865

PubMed Link: 30349879

Variant Present in the following documents:

• Main text
• RTH2-2-622.pdf

View BVdb publication page

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Genetic Mechanisms of Asthma and the Implications for Drug Repositioning.

Genes

Huo, Yue Y; Zhang, Hong-Yu HY

Publication Date: 2018-05-03

Variant appearance in text: rs3809865

PubMed Link: 29751569

Variant Present in the following documents:

• Main text
• genes-09-00237.pdf

View BVdb publication page

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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget

Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH

Publication Date: 2017-11-10

Variant appearance in text: rs3809865

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 4
• oncotarget-08-95841-s002.xlsx, sheet 1

View BVdb publication page

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Polymorphisms of microRNA target genes IL12B, INSR, CCND1 and IL10 in gastric cancer.

World Journal Of Gastroenterology

Petkevicius, Vytenis V; Salteniene, Violeta V; Juzenas, Simonas S; Wex, Thomas T; Link, Alexander A; Leja, Marcis M; Steponaitiene, Ruta R; Skieceviciene, Jurgita J; Kupcinskas, Limas L; Jonaitis, Laimas L; Kiudelis, Gediminas G; Malfertheiner, Peter P; Kupcinskas, Juozas J

Publication Date: 2017-05-21

Variant appearance in text: rs3809865

PubMed Link: 28596683

Variant Present in the following documents:

• Main text
• WJG-23-3480.pdf

View BVdb publication page

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Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases

Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ

Publication Date: 2017-05-23

Variant appearance in text: rs3809865

PubMed Link: 28535796

Variant Present in the following documents:

• 13023_2017_647_MOESM1_ESM.xlsx, sheet 4

View BVdb publication page

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Genetic polymorphisms of cell adhesion molecules in Behcet's disease in a Chinese Han population.

Scientific Reports

Zheng, Minming M; Zhang, Lijun L; Yu, Hongsong H; Hu, Jiayue J; Cao, Qingfeng Q; Huang, Guo G; Huang, Yang Y; Yuan, Gangxiang G; Kijlstra, Aize A; Yang, Peizeng P

Publication Date: 2016-04-25

Variant appearance in text: rs3809865

PubMed Link: 27108704

Variant Present in the following documents:

• Main text
• srep24974.pdf

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Genetic variants associated with colorectal brain metastases susceptibility and survival.

The Pharmacogenomics Journal

Stremitzer, S S; Berghoff, A S AS; Volz, N B NB; Zhang, W W; Yang, D D; Stintzing, S S; Ning, Y Y; Sunakawa, Y Y; Yamauchi, S S; Sebio, A A; Matsusaka, S S; Okazaki, S S; Hanna, D D; Parekh, A A; Mendez, A A; Berger, M D MD; El-Khoueiry, R R; Birner, P P; Preusser, M M; Lenz, H-J HJ

Publication Date: 2017-01

Variant appearance in text: rs3809865

PubMed Link: 26689941

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrin beta-3 genetic variants and risk of venous thromboembolism in colorectal cancer patients.

Thrombosis Research

Bianconi, Daniela D; Schuler, Alexandra A; Pausz, Clemens C; Geroldinger, Angelika A; Kaider, Alexandra A; Lenz, Heinz-Josef HJ; Kornek, Gabriela G; Scheithauer, Werner W; Zielinski, Christoph C CC; Pabinger, Ingrid I; Ay, Cihan C; Prager, Gerald W GW

Publication Date: 2015-11

Variant appearance in text: rs3809865

PubMed Link: 26440977

Variant Present in the following documents:

• Main text
• nihms-1623477.pdf

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Association between polymorphisms in the integrin gene predicted microRNA binding sites and bladder cancer risk.

International Journal Of Clinical And Experimental Medicine

Liu, Jiaming J; Cheng, Sihang S; Zhang, Yonggang Y; Li, Hong H; Huang, Jin J; Zhang, Peng P

Publication Date: 2014

Variant appearance in text: rs3809865

PubMed Link: 25550960

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variants in microRNA target sites of 37 selected cancer-related genes and the risk of cervical cancer.

Plos One

Mi, Yang Y; Wang, Lijuan L; Zong, Lu L; Pei, Meili M; Lu, Qingyang Q; Huang, Pu P

Publication Date: 2014

Variant appearance in text: rs3809865

PubMed Link: 24465869

Variant Present in the following documents:

• Main text
• pone.0086061.pdf

View BVdb publication page

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Genetic variation of ITGB3 is associated with asthma in Chinese Han children.

Plos One

Zhang, Yan Y; Han, Yuling Y; Dong, Liang L; Yu, Huafeng H; Cheng, Lu L; Zhao, Xiuxia X; Ding, Mingjie M

Publication Date: 2013

Variant appearance in text: rs3809865

PubMed Link: 23451109

Variant Present in the following documents:

• Main text
• pone.0056914.pdf

View BVdb publication page

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Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.

European Journal Of Human Genetics : Ejhg

Napolioni, Valerio V; Lombardi, Federica F; Sacco, Roberto R; Curatolo, Paolo P; Manzi, Barbara B; Alessandrelli, Riccardo R; Militerni, Roberto R; Bravaccio, Carmela C; Lenti, Carlo C; Saccani, Monica M; Schneider, Cindy C; Melmed, Raun R; Pascucci, Tiziana T; Puglisi-Allegra, Stefano S; Reichelt, Karl-Ludvig KL; Rousseau, Francis F; Lewin, Patricia P; Persico, Antonio M AM

Publication Date: 2011-03

Variant appearance in text: rs3809865

PubMed Link: 21102624

Variant Present in the following documents:

• Main text

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High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

Bmc Genetics

Daelemans, Caroline C; Ritchie, Matthew E ME; Smits, Guillaume G; Abu-Amero, Sayeda S; Sudbery, Ian M IM; Forrest, Matthew S MS; Campino, Susana S; Clark, Taane G TG; Stanier, Philip P; Kwiatkowski, Dominic D; Deloukas, Panos P; Dermitzakis, Emmanouil T ET; Tavaré, Simon S; Moore, Gudrun E GE; Dunham, Ian I

Publication Date: 2010-04-19

Variant appearance in text: rs3809865

PubMed Link: 20403199

Variant Present in the following documents:

• Main text
• 1471-2156-11-25.pdf

View BVdb publication page

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Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction.

American Heart Journal

Knowles, Joshua W JW; Wang, Huijan H; Itakura, Haruka H; Southwick, Audrey A; Myers, Richard M RM; Iribarren, Carlos C; Fortmann, Stephen P SP; Go, Alan S AS; Quertermous, Thomas T; Hlatky, Mark A MA

Publication Date: 2007-12

Variant appearance in text: rs3809865

PubMed Link: 18035074

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.

American Journal Of Human Genetics

Mei, H H; Cuccaro, M L ML; Martin, E R ER

Publication Date: 2007-12

Variant appearance in text: rs3809865

PubMed Link: 17999363

Variant Present in the following documents:

• Main text

View BVdb publication page

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