Publications:

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Impact of pharmacogenetics on aspirin resistance: a systematic review.

Arquivos De Neuro-Psiquiatria

Silva, Gustavo Figueiredo da GFD; Lopes, Bruno Mattei BM; Moser, Vinicius V; Ferreira, Leslie Ecker LE

Publication Date: 2023-01

Variant appearance in text: rs1062535

PubMed Link: 36918009

Variant Present in the following documents:

• Main text
• 10-1055-s-0042-1758445.pdf

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Genetic Association Study and Machine Learning to Investigate Differences in Platelet Reactivity in Patients with Acute Ischemic Stroke Treated with Aspirin.

Biomedicines

Ikonnikova, Anna A; Anisimova, Anastasia A; Galkin, Sergey S; Gunchenko, Anastasia A; Abdukhalikova, Zhabikai Z; Filippova, Marina M; Surzhikov, Sergey S; Selyaeva, Lidia L; Shershov, Valery V; Zasedatelev, Alexander A; Avdonina, Maria M; Nasedkina, Tatiana T

Publication Date: 2022-10-13

Variant appearance in text: rs1062535

PubMed Link: 36289824

Variant Present in the following documents:

• Main text
• biomedicines-10-02564.pdf

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Simultaneous genotyping for human platelet antigen systems and HLA-A and HLA-B loci by targeted next-generation sequencing.

Frontiers In Immunology

Wang, Jielin J; You, Xuan X; He, Yanmin Y; Hong, Xiaozhen X; He, Ji J; Tao, Sudan S; Zhu, Faming F

Publication Date: 2022

Variant appearance in text: ITGA2: 825G>A; rs1062535

PubMed Link: 36263028

Variant Present in the following documents:

• Main text
• fimmu-13-945994.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: ITGA2: T275T

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM4_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2

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Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.

Journal Of The American Heart Association

Shi, Mengyao M; Kelly, Tanika N TN; Zhu, Zhengbao Z; Li, Changwei C; Shen, Chong C; Sun, Yingxian Y; Wang, Aili A; Shan, Guangliang G; Bu, Xiaoqing X; Guo, Daoxia D; Zhao, Jingbo J; Xu, Tan T; Peng, Hao H; Xu, Tian T; Zhong, Chongke C; Sun, Xiao X; Chen, Jing J; Zhang, Yonghong Y; He, Jiang J

Publication Date: 2022-10-04

Variant appearance in text: rs1062535

PubMed Link: 36193932

Variant Present in the following documents:

• JAH3-11-e025245.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: ITGA2: T275T

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM4_ESM.xlsx, sheet 2

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: N/A

PubMed Link: 35768426

Variant Present in the following documents:

View BVdb publication page

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Bacillus Calmette-Guérin Treatment Changes the Tumor Microenvironment of Non-Muscle-Invasive Bladder Cancer.

Frontiers In Oncology

Su, Fei F; Liu, Ming M; Zhang, Wei W; Tang, Min M; Zhang, Jinsong J; Li, Hexin H; Zou, Lihui L; Zhang, Rui R; Liu, Yudong Y; Li, Lin L; Ma, Jie J; Zhang, Yaqun Y; Chen, Meng M; Xiao, Fei F

Publication Date: 2022

Variant appearance in text: ITGA2: T275T

PubMed Link: 35311085

Variant Present in the following documents:

• Table_1.xlsx, sheet 4

View BVdb publication page

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A Bioinformatics Perspective on the Links Between Tetraspanin-Enriched Microdomains and Cardiovascular Pathophysiology.

Frontiers In Cardiovascular Medicine

Sun, Ge G; Chen, Junxiong J; Ding, Yingjun Y; Wren, Jonathan D JD; Xu, Fuyi F; Lu, Lu L; Wang, Yan Y; Wang, Dao-Wen DW; Zhang, Xin A XA

Publication Date: 2021

Variant appearance in text: rs1062535

PubMed Link: 33860000

Variant Present in the following documents:

• Main text
• fcvm-08-630471.pdf

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: N/A

PubMed Link: 33791233

Variant Present in the following documents:

View BVdb publication page

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Association of human platelet alloantigens encoding gene polymorphisms with the risk of Coronary artery disease in Iranian patients.

Bmc Cardiovascular Disorders

Malakootikhah, Farideh F; Naghavi, Hossein H; Firouzabadi, Negar N; Maadani, Mohsen M; Shafiei, Massoumeh M; Tajik, Nader N

Publication Date: 2021-02-02

Variant appearance in text: rs1062535

PubMed Link: 33530946

Variant Present in the following documents:

• Main text
• 12872_2021_Article_1892.pdf

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: N/A

PubMed Link: 32529721

Variant Present in the following documents:

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: N/A

PubMed Link: 32046637

Variant Present in the following documents:

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: N/A

PubMed Link: 31640808

Variant Present in the following documents:

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: ITGA2: T275T; rs1062535

PubMed Link: 31597922

Variant Present in the following documents:

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

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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: ITGA2: 825G>A

PubMed Link: 31189880

Variant Present in the following documents:

• 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1

View BVdb publication page

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Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall.

International Journal Of Molecular Sciences

Salinas-Torres, Víctor M VM; Gallardo-Blanco, Hugo L HL; Salinas-Torres, Rafael A RA; Cerda-Flores, Ricardo M RM; Lugo-Trampe, José J JJ; Villarreal-Martínez, Daniel Z DZ; Martínez de Villarreal, Laura E LE

Publication Date: 2019-05-09

Variant appearance in text: rs1062535

PubMed Link: 31075877

Variant Present in the following documents:

• Main text
• ijms-20-02295.pdf

View BVdb publication page

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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: rs1062535

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2

View BVdb publication page

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Revisiting aneuploidy profile of surgically retrieved spermatozoa by whole exome sequencing molecular karyotype.

Plos One

Cheung, Stephanie S; Schlegel, Peter N PN; Rosenwaks, Zev Z; Palermo, Gianpiero D GD

Publication Date: 2019

Variant appearance in text: ITGA2: 825G>A

PubMed Link: 30608972

Variant Present in the following documents:

• pone.0210079.s007.xlsx, sheet 21
• pone.0210079.s007.xlsx, sheet 18

View BVdb publication page

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Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports

Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS

Publication Date: 2018-12-04

Variant appearance in text: rs1062535

PubMed Link: 30514953

Variant Present in the following documents:

• 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1

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: ITGA2: 825G>A; rs1062535

PubMed Link: 30319441

Variant Present in the following documents:

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

View BVdb publication page

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A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine

Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H

Publication Date: 2018-09

Variant appearance in text: N/A

PubMed Link: 29974678

Variant Present in the following documents:

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: N/A

PubMed Link: 29221171

Variant Present in the following documents:

View BVdb publication page

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Cancer Stem Cell Gene Variants Predict Disease Recurrence in Patients Treated with Radical Prostatectomy for Prostate Cancer.

International Journal Of Medical Sciences

Lin, Victor C VC; Huang, Shu-Pin SP; Huang, Chao-Yuan CY; Yu, Chia-Cheng CC; Yin, Hsin-Ling HL; Huang, Tsung-Yi TY; Lee, Cheng-Hsueh CH; Lu, Te-Ling TL; Bao, Bo-Ying BY

Publication Date: 2017

Variant appearance in text: rs1062535

PubMed Link: 29104488

Variant Present in the following documents:

• Main text
• ijmsv14p1301.pdf

View BVdb publication page

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Massive bleeding in cardiac surgery. Definitions, predictors and challenges.

Hippokratia

Petrou, A A; Tzimas, P P; Siminelakis, S S

Publication Date: 2016

Variant appearance in text: rs1062535

PubMed Link: 29097882

Variant Present in the following documents:

• Main text

View BVdb publication page

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GPla Polymorphisms Are Associated with Outcomes in Patients at High Cardiovascular Risk.

Frontiers In Cardiovascular Medicine

Rath, Dominik D; Schaeffeler, Elke E; Winter, Stefan S; Levertov, Semjon S; Müller, Karin K; Droppa, Michal M; Stimpfle, Fabian F; Langer, Harald F HF; Gawaz, Meinrad M; Schwab, Matthias M; Geisler, Tobias T

Publication Date: 2017

Variant appearance in text: rs1062535

PubMed Link: 28871283

Variant Present in the following documents:

• Main text
• fcvm-04-00052.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: rs1062535

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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New single-nucleotide polymorphisms associated with differences in platelet reactivity and their influence on survival in patients with type 2 diabetes treated with acetylsalicylic acid: an observational study.

Acta Diabetologica

Milanowski, Lukasz L; Pordzik, Justyna J; Janicki, Piotr K PK; Kaplon-Cieslicka, Agnieszka A; Rosiak, Marek M; Peller, Michal M; Tyminska, Agata A; Ozieranski, Krzysztof K; Filipiak, Krzysztof J KJ; Opolski, Grzegorz G; Mirowska-Guzel, Dagmara D; Postula, Marek M

Publication Date: 2017-04

Variant appearance in text: rs1062535

PubMed Link: 27995340

Variant Present in the following documents:

• Main text
• 592_2016_Article_945.pdf

View BVdb publication page

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Gene variants as risk factors for gastroschisis.

American Journal Of Medical Genetics. Part A

Padula, Amy M AM; Yang, Wei W; Schultz, Kathleen K; Tom, Lauren L; Lin, Bin B; Carmichael, Suzan L SL; Lammer, Edward J EJ; Shaw, Gary M GM

Publication Date: 2016-11

Variant appearance in text: rs1062535

PubMed Link: 27616475

Variant Present in the following documents:

• Main text
• AJMG-170-2788.pdf

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: N/A

PubMed Link: 25944692

Variant Present in the following documents:

View BVdb publication page

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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:

View BVdb publication page

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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:

View BVdb publication page

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Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.

Plos One

Patiño, Liliana Catherine LC; Battu, Rajani R; Ortega-Recalde, Oscar O; Nallathambi, Jeyabalan J; Anandula, Venkata Ramana VR; Renukaradhya, Umashankar U; Laissue, Paul P

Publication Date: 2014

Variant appearance in text: N/A

PubMed Link: 25333361

Variant Present in the following documents:

View BVdb publication page

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Association of CVD candidate gene polymorphisms with ischemic stroke and cerebral hemorrhage in Chinese individuals.

Plos One

Ou, Wenjing W; Liu, Xin X; Shen, Yue Y; Li, Jiana J; He, Lingbin L; Yuan, Yuan Y; Tan, Xuerui X; Liu, Lisheng L; Zhao, Jingbo J; Wang, Xingyu X

Publication Date: 2014

Variant appearance in text: rs1062535

PubMed Link: 25144711

Variant Present in the following documents:

• Main text
• pone.0105516.pdf

View BVdb publication page

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Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.

Cancer Science

Nasuno, Tomomitsu T; Mimaki, Sachiyo S; Okamoto, Makito M; Esumi, Hiroyasu H; Tsuchihara, Katsuya K

Publication Date: 2014-02

Variant appearance in text: N/A

PubMed Link: 24219164

Variant Present in the following documents:

View BVdb publication page

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Novel risk factors for premature peripheral arterial occlusive disease in non-diabetic patients: a case-control study.

Plos One

Bérard, Annie M AM; Bedel, Aurélie A; Le Trequesser, Rémi R; Freyburger, Geneviève G; Nurden, Alan A; Colomer, Sylvie S; Guérin, Viviane V; Vergnes, Marie-Christine MC; Becker, François F; Camelot, Gabriel G; Bressolette, Luc L; Lacroix, Philippe P; Cambou, Jean-Pierre JP; Bura-Rivière, Alessandra A; Emmerich, Joseph J; Darmon, Michel M; Deletraz, Anne-Marie AM; Mesli, Samir S; Colombies, Brigitte B; Vanbrugghe, Virginie V; Conri, Claude C; Constans, Joël J

Publication Date: 2013

Variant appearance in text: rs1062535

PubMed Link: 23533563

Variant Present in the following documents:

• Main text
• pone.0037882.pdf

View BVdb publication page

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Large-scale gene-centric analysis identifies novel variants for coronary artery disease.

Plos Genetics

,

Publication Date: 2011-09

Variant appearance in text: rs1062535

PubMed Link: 21966275

Variant Present in the following documents:

• Main text
• pgen.1002260.s008.pdf
• pgen.1002260.pdf

View BVdb publication page

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Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years.

American Journal Of Obstetrics And Gynecology

Clark, Erin A S EA; Mele, Lisa L; Wapner, Ronald J RJ; Spong, Catherine Y CY; Sorokin, Yoram Y; Peaceman, Alan A; Iams, Jay D JD; Leveno, Kenneth J KJ; Harper, Margaret M; Caritis, Steve N SN; Miodovnik, Menachem M; Mercer, Brian M BM; Thorp, John M JM; Ramin, Susan M SM; Carpenter, Marshall M; Rouse, Dwight J DJ; ,

Publication Date: 2010-07

Variant appearance in text: rs1062535

PubMed Link: 20417488

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Birth Defects Research. Part A, Clinical And Molecular Teratology

Kuehl, Karen K; Loffredo, Christopher C; Lammer, Edward J EJ; Iovannisci, David M DM; Shaw, Gary M GM

Publication Date: 2010-02

Variant appearance in text: rs1062535

PubMed Link: 19764075

Variant Present in the following documents:

• Main text

View BVdb publication page

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A candidate gene association study of 77 polymorphisms in migraine.

The Journal Of Pain

Schürks, Markus M; Kurth, Tobias T; Buring, Julie E JE; Zee, Robert Y L RY

Publication Date: 2009-07

Variant appearance in text: rs1062535

PubMed Link: 19559392

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.

Journal Of Hypertension

Conen, David D; Cheng, Suzanne S; Steiner, Lori L LL; Buring, Julie E JE; Ridker, Paul M PM; Zee, Robert Y L RY

Publication Date: 2009-03

Variant appearance in text: rs1062535

PubMed Link: 19330901

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.

Clinica Chimica Acta; International Journal Of Clinical Chemistry

Zee, Robert Y L RY; Bubes, Vadim V; Shrivastava, Sanjay S; Ridker, Paul M PM; Glynn, Robert J RJ

Publication Date: 2009-04

Variant appearance in text: rs1062535

PubMed Link: 19263529

Variant Present in the following documents:

• Main text

View BVdb publication page

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A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

Stroke

Wang, Xingyu X; Cheng, Suzanne S; Brophy, Victoria H VH; Erlich, Henry A HA; Mannhalter, Christine C; Berger, Klaus K; Lalouschek, Wolfgang W; Browner, Warren S WS; Shi, Yu Y; Ringelstein, E Bernd EB; Kessler, Christof C; Luedemann, Jan J; Lindpaintner, Klaus K; Liu, Lisheng L; Ridker, Paul M PM; Zee, Robert Y L RY; Cook, Nancy R NR; ,

Publication Date: 2009-03

Variant appearance in text: rs1062535

PubMed Link: 19131662

Variant Present in the following documents:

• Main text

View BVdb publication page

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Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease.

European Journal Of Human Genetics : Ejhg

FitzGerald, Liesel M LM; Patterson, Briony B; Thomson, Russell R; Polanowski, Andrea A; Quinn, Stephen S; Brohede, Jesper J; Thornton, Timothy T; Challis, David D; Mackey, David A DA; Dwyer, Terence T; Foote, Simon S; Hannan, Garry N GN; Stankovich, James J; McKay, James D JD; Dickinson, Joanne L JL

Publication Date: 2009-03

Variant appearance in text: rs1062535

PubMed Link: 18830231

Variant Present in the following documents:

• Main text

View BVdb publication page

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New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

Bmc Bioinformatics

Penco, Silvana S; Buscema, Massimo M; Patrosso, Maria Cristina MC; Marocchi, Alessandro A; Grossi, Enzo E

Publication Date: 2008-05-30

Variant appearance in text: rs1062535

PubMed Link: 18513389

Variant Present in the following documents:

• Main text
• 1471-2105-9-254.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: rs1062535

PubMed Link: 18035074

Variant Present in the following documents:

• Main text

View BVdb publication page

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