COL1A1 c.804+80A>C

Variant ID: 17-48274291-T-G

NM_000088.3(COL1A1):c.804+80A>C

This variant was identified in 42 publications

View GRCh38 version.




Publications:


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: rs2075555
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



Mutation analysis of the WFS1 gene in a Chinese family with autosomal-dominant non-syndrome deafness.

Scientific Reports
Zhao, Jing J; Zhang, Siqi S; Jiang, Yuan Y; Liu, Yan Y; Wang, Jiantao J; Zhu, QingWen Q
Publication Date: 2022-12-23

Variant appearance in text: rs2075555
PubMed Link: 36564540
Variant Present in the following documents:
  • 41598_2022_26850_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



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: rs2075555
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss.

Plos One
Lei, Peiliang P; Zhu, Qingwen Q; Dong, Wenrong W; Zhang, Siqi S; Sun, Yanyan Y; Du, Xitong X; Geng, Meng M; Jiang, Yuan Y
Publication Date: 2022

Variant appearance in text: rs2075555
PubMed Link: 36350814
Variant Present in the following documents:
  • pone.0276233.s004.xlsx, sheet 1
View BVdb publication page



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: rs2075555
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



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: rs2075555
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



A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family.

Bmc Medical Genomics
Li, Qiong Q; Wang, Shujuan S; Liang, Pengfei P; Li, Wei W; Wang, Jian J; Fan, Bei B; Yang, Yang Y; An, Xiaogang X; Chen, Jun J; Zha, Dingjun D
Publication Date: 2022-07-21

Variant appearance in text: rs2075555
PubMed Link: 35864542
Variant Present in the following documents:
  • 12920_2022_1315_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Utility of next-generation sequencing in genetic testing and counseling of disorders involving the musculoskeletal system-trends observed from a single genetic unit.

Journal Of Orthopaedic Surgery And Research
Iyer, Gayatri R GR; Kumar, Roshan R; Poornima, Subhadra S; Kamireddy, Aruna Priya AP; Juturu, Keerthi Konda KK; Bhatnagar, Lekhangda L; Arora, Srinka S; Suresh, Vaishnavi V; Utage, Prashant R PR; Bailur, Sarah S; Pujar, Akhilesh N AN; Hasan, Qurratulain Q
Publication Date: 2022-02-05

Variant appearance in text: rs2075555
PubMed Link: 35123515
Variant Present in the following documents:
  • Main text
  • 13018_2022_Article_2969.pdf
View BVdb publication page



Utility of next-generation sequencing in genetic testing and counseling of disorders involving the musculoskeletal system-trends observed from a single genetic unit.

Journal Of Orthopaedic Surgery And Research
Iyer, Gayatri R GR; Kumar, Roshan R; Poornima, Subhadra S; Kamireddy, Aruna Priya AP; Juturu, Keerthi Konda KK; Bhatnagar, Lekhangda L; Arora, Srinka S; Suresh, Vaishnavi V; Utage, Prashant R PR; Bailur, Sarah S; Pujar, Akhilesh N AN; Hasan, Qurratulain Q
Publication Date: 2022-02-05

Variant appearance in text: rs2075555
PubMed Link: 35123515
Variant Present in the following documents:
  • Main text
  • 13018_2022_Article_2969.pdf
View BVdb publication page



The Role of Polymorphisms in Collagen-Encoding Genes in Intervertebral Disc Degeneration.

Biomolecules
Trefilova, Vera V VV; Shnayder, Natalia A NA; Petrova, Marina M MM; Kaskaeva, Daria S DS; Tutynina, Olga V OV; Petrov, Kirill V KV; Popova, Tatiana E TE; Balberova, Olga V OV; Medvedev, German V GV; Nasyrova, Regina F RF
Publication Date: 2021-08-26

Variant appearance in text: rs2075555
PubMed Link: 34572492
Variant Present in the following documents:
  • Main text
  • biomolecules-11-01279.pdf
View BVdb publication page



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: COL1A1: 804+80A>C; rs2075555
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Delineation of the Germline and Somatic Mutation Interaction Landscape in Triple-Negative and Non-Triple-Negative Breast Cancer.

International Journal Of Genomics
Wu, Jiande J; Mamidi, Tarun K K TKK; Zhang, Lu L; Hicks, Chindo C
Publication Date: 2020

Variant appearance in text: rs2075555
PubMed Link: 32724790
Variant Present in the following documents:
  • Main text
  • IJG2020-2641370.pdf
View BVdb publication page



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: COL1A1: 804+80A>C; rs2075555
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



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: rs2075555
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data.

Breast Cancer Research : Bcr
Melloni, Giorgio E M GEM; Mazzarella, Luca L; Bernard, Loris L; Bodini, Margherita M; Russo, Anna A; Luzi, Lucilla L; Pelicci, Pier Giuseppe PG; Riva, Laura L
Publication Date: 2017-05-31

Variant appearance in text: rs2075555
PubMed Link: 28569218
Variant Present in the following documents:
  • 13058_2017_854_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Genetic Factors in Intervertebral Disc Degeneration.

Genes & Diseases
Feng, Yi Y; Egan, Brian B; Wang, Jinxi J
Publication Date: 2016-09

Variant appearance in text: rs2075555
PubMed Link: 27617275
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic association of COL1A1 polymorphisms with high myopia in Asian population: a Meta-analysis.

International Journal Of Ophthalmology
Gong, Bo B; Qu, Chao C; Huang, Xiao-Fang XF; Ye, Zi-Meng ZM; Zhang, Ding-Ding DD; Shi, Yi Y; Chen, Rong R; Liu, Yu-Ping YP; Shuai, Ping P
Publication Date: 2016

Variant appearance in text: rs2075555
PubMed Link: 27588274
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of COL1A1 polymorphism with high myopia: a Meta-analysis.

International Journal Of Ophthalmology
Jin, Guang-Ming GM; Zhao, Xiao-Jing XJ; Chen, Ai-Ming AM; Chen, Yong-Xing YX; Li, Qin Q
Publication Date: 2016

Variant appearance in text: rs2075555
PubMed Link: 27162737
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs2075555
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 3
View BVdb publication page



Association between COL1A1 polymorphisms and high myopia: a meta-analysis.

International Journal Of Clinical And Experimental Medicine
Zhang, Xiaoyu X; Zhou, Xingtao X; Qu, Xinhua X
Publication Date: 2015

Variant appearance in text: rs2075555
PubMed Link: 26131177
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic risk variants associated with in situ breast cancer.

Breast Cancer Research : Bcr
Campa, Daniele D; Barrdahl, Myrto M; Gaudet, Mia M MM; Black, Amanda A; Chanock, Stephen J SJ; Diver, W Ryan WR; Gapstur, Susan M SM; Haiman, Christopher C; Hankinson, Susan S; Hazra, Aditi A; Henderson, Brian B; Hoover, Robert N RN; Hunter, David J DJ; Joshi, Amit D AD; Kraft, Peter P; Le Marchand, Loic L; Lindström, Sara S; Willett, Walter W; Travis, Ruth C RC; Amiano, Pilar P; Siddiq, Afshan A; Trichopoulos, Dimitrios D; Sund, Malin M; Tjønneland, Anne A; Weiderpass, Elisabete E; Peeters, Petra H PH; Panico, Salvatore S; Dossus, Laure L; Ziegler, Regina G RG; Canzian, Federico F; Kaaks, Rudolf R
Publication Date: 2015-06-13

Variant appearance in text: rs2075555
PubMed Link: 26070784
Variant Present in the following documents:
  • Main text
  • 13058_2015_Article_596.pdf
View BVdb publication page



Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women.

Human Molecular Genetics
Barrdahl, Myrto M; Canzian, Federico F; Joshi, Amit D AD; Travis, Ruth C RC; Chang-Claude, Jenny J; Auer, Paul L PL; Gapstur, Susan M SM; Gaudet, Mia M; Diver, W Ryan WR; Henderson, Brian E BE; Haiman, Christopher A CA; Schumacher, Fredrick R FR; Le Marchand, Loïc L; Berg, Christine D CD; Chanock, Stephen J SJ; Hoover, Robert N RN; Rudolph, Anja A; Ziegler, Regina G RG; Giles, Graham G GG; Baglietto, Laura L; Severi, Gianluca G; Hankinson, Susan E SE; Lindström, Sara S; Willet, Walter W; Hunter, David J DJ; Buring, Julie E JE; Lee, I-Min IM; Zhang, Shumin S; Dossus, Laure L; Cox, David G DG; Khaw, Kay-Tee KT; Lund, Eiliv E; Naccarati, Alessio A; Peeters, Petra H PH; Quirós, J Ramón JR; Riboli, Elio E; Sund, Malin M; Trichopoulos, Dimitrios D; Prentice, Ross L RL; Kraft, Peter P; Kaaks, Rudolf R; Campa, Daniele D
Publication Date: 2014-10-01

Variant appearance in text: rs2075555
PubMed Link: 24895409
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common breast cancer risk variants in the post-COGS era: a comprehensive review.

Breast Cancer Research : Bcr
Maxwell, Kara N KN; Nathanson, Katherine L KL
Publication Date: 2013-12-20

Variant appearance in text: rs2075555
PubMed Link: 24359602
Variant Present in the following documents:
  • Main text
View BVdb publication page



Breast cancer prediction using genome wide single nucleotide polymorphism data.

Bmc Bioinformatics
Hajiloo, Mohsen M; Damavandi, Babak B; Hooshsadat, Metanat M; Sangi, Farzad F; Mackey, John R JR; Cass, Carol E CE; Greiner, Russell R; Damaraju, Sambasivarao S
Publication Date: 2013

Variant appearance in text: rs2075555
PubMed Link: 24266904
Variant Present in the following documents:
  • Main text
  • 1471-2105-14-S13-S3.pdf
View BVdb publication page



Candidate gene analysis in israeli soldiers with stress fractures.

Journal Of Sports Science & Medicine
Yanovich, Ran R; Friedman, Eitan E; Milgrom, Roni R; Oberman, Bernice B; Freedman, Laurence L; Moran, Daniel S DS
Publication Date: 2012

Variant appearance in text: rs2075555
PubMed Link: 24149131
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel Integrative Genomics Approach for Associating GWAS Information with Intrinsic Subtypes of Breast Cancer.

Cancer Informatics
Hicks, Chindo C; Koganti, Tejaswi T; Brown, Alexandra S AS; Monico, Jesus J; Backus, Kandis K; Miele, Lucio L
Publication Date: 2013

Variant appearance in text: rs2075555
PubMed Link: 23761956
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm.

Plos One
Sapkota, Yadav Y; Yasui, Yutaka Y; Lai, Raymond R; Sridharan, Malinee M; Robson, Paula J PJ; Cass, Carol E CE; Mackey, John R JR; Damaraju, Sambasivarao S
Publication Date: 2013

Variant appearance in text: rs2075555
PubMed Link: 23717390
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic polymorphisms associated with intervertebral disc degeneration.

The Spine Journal : Official Journal Of The North American Spine Society
Mayer, Jillian E JE; Iatridis, James C JC; Chan, Danny D; Qureshi, Sheeraz A SA; Gottesman, Omri O; Hecht, Andrew C AC
Publication Date: 2013-03

Variant appearance in text: rs2075555
PubMed Link: 23537453
Variant Present in the following documents:
  • Main text
View BVdb publication page



An Integrative Genomics Approach for Associating GWAS Information with Triple-Negative Breast Cancer.

Cancer Informatics
Hicks, Chindo C; Kumar, Ranjit R; Pannuti, Antonio A; Backus, Kandis K; Brown, Alexandra A; Monico, Jesus J; Miele, Lucio L
Publication Date: 2013

Variant appearance in text: rs2075555
PubMed Link: 23423317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association studies in lumbar disc degeneration: a systematic review.

Plos One
Eskola, Pasi J PJ; Lemmelä, Susanna S; Kjaer, Per P; Solovieva, Svetlana S; Männikkö, Minna M; Tommerup, Niels N; Lind-Thomsen, Allan A; Husgafvel-Pursiainen, Kirsti K; Cheung, Kenneth M C KM; Chan, Danny D; Samartzis, Dino D; Karppinen, Jaro J
Publication Date: 2012

Variant appearance in text: rs2075555
PubMed Link: 23185509
Variant Present in the following documents:
  • Main text
  • pone.0049995.pdf
View BVdb publication page



An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration.

The Open Orthopaedics Journal
Omair, Ahmad A; Lie, Benedicte Alexandra BA; Reikeras, Olav O; Brox, Jens Ivar JI
Publication Date: 2012

Variant appearance in text: rs2075555
PubMed Link: 22550553
Variant Present in the following documents:
  • Main text
View BVdb publication page



Integrative Analysis of Response to Tamoxifen Treatment in ER-Positive Breast Cancer Using GWAS Information and Transcription Profiling.

Breast Cancer : Basic And Clinical Research
Hicks, Chindo C; Kumar, Ranjit R; Pannuti, Antonio A; Miele, Lucio L
Publication Date: 2012

Variant appearance in text: rs2075555
PubMed Link: 22399860
Variant Present in the following documents:
  • Main text
View BVdb publication page



An association study of the COL1A1 gene and high myopia in a Han Chinese population.

Molecular Vision
Zhang, Dingding D; Shi, Yi Y; Gong, Bo B; He, Fei F; Lu, Fang F; Lin, He H; Wu, Zhengzheng Z; Cheng, Jing J; Chen, Bin B; Liao, Shihuang S; Ma, Shi S; Hu, Jianbin J; Yang, Zhenglin Z
Publication Date: 2011

Variant appearance in text: rs2075555
PubMed Link: 22219633
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common genetic variants are associated with accelerated bone mineral density loss after hematopoietic cell transplantation.

Plos One
Yao, Song S; Sucheston, Lara E LE; Smiley, Shannon L SL; Davis, Warren W; Conroy, Jeffrey M JM; Nowak, Norma J NJ; Ambrosone, Christine B CB; McCarthy, Philip L PL; Hahn, Theresa T
Publication Date: 2011

Variant appearance in text: rs2075555
PubMed Link: 22022476
Variant Present in the following documents:
  • Main text
View BVdb publication page



An integrative genomics approach to biomarker discovery in breast cancer.

Cancer Informatics
Hicks, Chindo C; Asfour, Rozana R; Pannuti, Antonio A; Miele, Lucio L
Publication Date: 2011

Variant appearance in text: rs2075555
PubMed Link: 21869864
Variant Present in the following documents:
  • Main text
  • cin-10-2011-185.pdf
View BVdb publication page



Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium.

Journal Of The National Cancer Institute
Campa, Daniele D; Kaaks, Rudolf R; Le Marchand, Loïc L; Haiman, Christopher A CA; Travis, Ruth C RC; Berg, Christine D CD; Buring, Julie E JE; Chanock, Stephen J SJ; Diver, W Ryan WR; Dostal, Lucie L; Fournier, Agnes A; Hankinson, Susan E SE; Henderson, Brian E BE; Hoover, Robert N RN; Isaacs, Claudine C; Johansson, Mattias M; Kolonel, Laurence N LN; Kraft, Peter P; Lee, I-Min IM; McCarty, Catherine A CA; Overvad, Kim K; Panico, Salvatore S; Peeters, Petra H M PH; Riboli, Elio E; Sanchez, Maria José MJ; Schumacher, Fredrick R FR; Skeie, Guri G; Stram, Daniel O DO; Thun, Michael J MJ; Trichopoulos, Dimitrios D; Zhang, Shumin S; Ziegler, Regina G RG; Hunter, David J DJ; Lindström, Sara S; Canzian, Federico F
Publication Date: 2011-08-17

Variant appearance in text: rs2075555
PubMed Link: 21791674
Variant Present in the following documents:
  • Main text
View BVdb publication page



No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women.

Acta Pharmacologica Sinica
Hu, Wei-wei WW; He, Jin-wei JW; Zhang, Hao H; Wang, Chun C; Gu, Jie-mei JM; Yue, Hua H; Ke, Yao-hua YH; Hu, Yun-qiu YQ; Fu, Wen-zhen WZ; Li, Miao M; Liu, Yu-juan YJ; Zhang, Zhen-lin ZL
Publication Date: 2011-07

Variant appearance in text: rs2075555
PubMed Link: 21602843
Variant Present in the following documents:
  • Main text
View BVdb publication page



Nature and nurture: the complex genetics of myopia and refractive error.

Clinical Genetics
Wojciechowski, R R
Publication Date: 2011-04

Variant appearance in text: rs2075555
PubMed Link: 21155761
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variant in myocilin gene is associated with high myopia in isolated population of Korcula Island, Croatia.

Croatian Medical Journal
Vatavuk, Zoran Z; Skunca Herman, Jelena J; Bencić, Goran G; Andrijević Derk, Biljana B; Lacmanović Loncar, Valentina V; Petric Vicković, Ivanka I; Bucan, Kajo K; Mandić, Kresimir K; Mandić, Antonija A; Skegro, Ivan I; Pavicić Astalos, Jasna J; Merc, Ivana I; Martinović, Miljenka M; Kralj, Petra P; Knezević, Tamara T; Barać-Juretić, Katja K; Zgaga, Lina L
Publication Date: 2009-02

Variant appearance in text: rs2075555
PubMed Link: 19260140
Variant Present in the following documents:
  • Main text
View BVdb publication page



Molecular genetics of human myopia: an update.

Optometry And Vision Science : Official Publication Of The American Academy Of Optometry
Young, Terri L TL
Publication Date: 2009-01

Variant appearance in text: rs2075555
PubMed Link: 19104467
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.

Bmc Medical Genetics
Murabito, Joanne M JM; Rosenberg, Carol L CL; Finger, Daniel D; Kreger, Bernard E BE; Levy, Daniel D; Splansky, Greta Lee GL; Antman, Karen K; Hwang, Shih-Jen SJ
Publication Date: 2007-09-19

Variant appearance in text: rs2075555
PubMed Link: 17903305
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association with bone mass and geometry in the Framingham Heart Study.

Bmc Medical Genetics
Kiel, Douglas P DP; Demissie, Serkalem S; Dupuis, Josée J; Lunetta, Kathryn L KL; Murabito, Joanne M JM; Karasik, David D
Publication Date: 2007-09-19

Variant appearance in text: rs2075555
PubMed Link: 17903296
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S14.pdf
View BVdb publication page