Publications:

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A case of midbrain germinoma: A literature review for radiographic and clinical features.

Neuro-Oncology Advances

Miyake, Yohei Y; Tateishi, Kensuke K; Oshima, Akito A; Hongo, Takeshi T; Satomi, Kaishi K; Ichimura, Koichi K; Kato, Ayumi A; Iwashita, Hiromichi H; Utsunomiya, Daisuke D; Yamamoto, Tetsuya T

Publication Date: 2023

Variant appearance in text: FUT3: 1067T>A; Ile356Lys; rs3894326

PubMed Link: 37215953

Variant Present in the following documents:

• vdad043_suppl_supplementary_tables.xlsx, sheet 1

View BVdb publication page

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Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications

Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA

Publication Date: 2023-04-03

Variant appearance in text: FUT3: I356K

PubMed Link: 37012232

Variant Present in the following documents:

• 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2

View BVdb publication page

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Fluorescence Melting Curve Analysis for Concurrent Genotyping of Three Tag SNPs in FUT3.

Diagnostics (Basel, Switzerland)

Soejima, Mikiko M; Koda, Yoshiro Y

Publication Date: 2022-12-04

Variant appearance in text: FUT3: 1067T>A; Ile356Lys; rs3894326

PubMed Link: 36553046

Variant Present in the following documents:

• Main text
• diagnostics-12-03039.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: FUT3: I356K

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM8_ESM.xlsx, sheet 2

View BVdb publication page

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Validation of a genotype-based algorithm that identifies individuals with low, intermediate, and high serum CA19-9 levels in cancer-free individuals and in patients with colorectal cancer.

Journal Of Gastrointestinal Oncology

Wannhoff, Andreas A; Werner, Simone S; Tao, Sha S; Brenner, Hermann H; Gotthardt, Daniel N DN

Publication Date: 2022-08

Variant appearance in text: rs3894326

PubMed Link: 36092337

Variant Present in the following documents:

• Main text
• jgo-13-04-1711.pdf

View BVdb publication page

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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: FUT3: I356K; rs3894326

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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ABO, secretor, and Lewis carbohydrate histo-blood groups are associated with autoimmune neutropenia of early childhood in Danish patients.

Transfusion

Kløve-Mogensen, Kirstine K; Steffensen, Rudi R; Masmas, Tania Nicole TN; Glenthøj, Andreas A; Haunstrup, Thure Mors TM; Ratcliffe, Paul P; Höglund, Petter P; Hasle, Henrik H; Nielsen, Kaspar René KR

Publication Date: 2022-08

Variant appearance in text: rs3894326

PubMed Link: 35792132

Variant Present in the following documents:

• Main text
• TRF-62-1636.pdf

View BVdb publication page

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The Influence of FUT2 and FUT3 Polymorphisms and Nasopharyngeal Microbiome on Respiratory Infections in Breastfed Bangladeshi Infants from the Microbiota and Health Study.

Msphere

Binia, Aristea A; Siegwald, Léa L; Sultana, Shamima S; Shevlyakova, Maya M; Lefebvre, Gregory G; Foata, Francis F; Combremont, Séverine S; Charpagne, Aline A; Vidal, Karine K; Sprenger, Norbert N; Rahman, Mahbubar M; Palleja, Albert A; Eklund, Aron C AC; Nielsen, Henrik Bjørn HB; Brüssow, Harald H; Sarker, Shafiqul Alam SA; Sakwinska, Olga O

Publication Date: 2021-12-22

Variant appearance in text: rs3894326

PubMed Link: 34756056

Variant Present in the following documents:

• Main text
• msphere.00686-21.pdf

View BVdb publication page

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The Influence of FUT2 and FUT3 Polymorphisms and Nasopharyngeal Microbiome on Respiratory Infections in Breastfed Bangladeshi Infants from the Microbiota and Health Study.

Msphere

Binia, Aristea A; Siegwald, Léa L; Sultana, Shamima S; Shevlyakova, Maya M; Lefebvre, Gregory G; Foata, Francis F; Combremont, Séverine S; Charpagne, Aline A; Vidal, Karine K; Sprenger, Norbert N; Rahman, Mahbubar M; Palleja, Albert A; Eklund, Aron C AC; Nielsen, Henrik Bjørn HB; Brüssow, Harald H; Sarker, Shafiqul Alam SA; Sakwinska, Olga O

Publication Date: 2021-11-10

Variant appearance in text: rs3894326

PubMed Link: 34756056

Variant Present in the following documents:

• Main text
• msphere.00686-21.pdf

View BVdb publication page

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Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Molecular & Cellular Proteomics : Mcp

Schmitt, Marisa M; Sinnberg, Tobias T; Bratl, Katrin K; Zittlau, Katharina K; Garbe, Claus C; Macek, Boris B; Nalpas, Nicolas C NC

Publication Date: 2021

Variant appearance in text: FUT3: I356K; rs3894326

PubMed Link: 34673281

Variant Present in the following documents:

• mmc2.xlsx, sheet 11
• mmc2.xlsx, sheet 3

View BVdb publication page

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Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Molecular & Cellular Proteomics : Mcp

Schmitt, Marisa M; Sinnberg, Tobias T; Bratl, Katrin K; Zittlau, Katharina K; Garbe, Claus C; Macek, Boris B; Nalpas, Nicolas C NC

Publication Date: 2021-10-19

Variant appearance in text: FUT3: I356K; rs3894326

PubMed Link: 34673281

Variant Present in the following documents:

• mmc2.xlsx, sheet 3
• mmc2.xlsx, sheet 11

View BVdb publication page

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Evaluating the Robustness of Biomarkers of Dairy Food Intake in a Free-Living Population Using Single- and Multi-Marker Approaches.

Metabolites

Li, Katherine J KJ; Burton-Pimentel, Kathryn J KJ; Brouwer-Brolsma, Elske M EM; Feskens, Edith J M EJM; Blaser, Carola C; Badertscher, René R; Portmann, Reto R; Vergères, Guy G

Publication Date: 2021-06-17

Variant appearance in text: rs3894326

PubMed Link: 34204298

Variant Present in the following documents:

• Main text
• metabolites-11-00395.pdf

View BVdb publication page

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Association between ABO and Duffy blood types and circulating chemokines and cytokines.

Genes And Immunity

Van Alsten, Sarah C SC; Aversa, John G JG; Santo, Loredana L; Camargo, M Constanza MC; Kemp, Troy T; Liu, Jia J; Huang, Wen-Yi WY; Sampson, Joshua J; Rabkin, Charles S CS

Publication Date: 2021-07

Variant appearance in text: rs3894326

PubMed Link: 34103707

Variant Present in the following documents:

• Main text
• 41435_2021_Article_137.pdf

View BVdb publication page

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Association between ABO and Duffy blood types and circulating chemokines and cytokines.

Genes And Immunity

Van Alsten, Sarah C SC; Aversa, John G JG; Santo, Loredana L; Camargo, M Constanza MC; Kemp, Troy T; Liu, Jia J; Huang, Wen-Yi WY; Sampson, Joshua J; Rabkin, Charles S CS

Publication Date: 2021-07

Variant appearance in text: rs3894326

PubMed Link: 34103707

Variant Present in the following documents:

• Main text
• 41435_2021_Article_137.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: FUT3: Ile356Lys; rs3894326

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss.

Bmc Medical Genomics

Yang, Guangxian G; Yin, Yi Y; Tan, Zhiping Z; Liu, Jian J; Deng, Xicheng X; Yang, Yifeng Y

Publication Date: 2021-01-21

Variant appearance in text: FUT3: 1067T>A; I356K; rs3894326

PubMed Link: 33478437

Variant Present in the following documents:

• 12920_2021_871_MOESM2_ESM.xls, sheet 1

View BVdb publication page

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Time of Lactation and Maternal Fucosyltransferase Genetic Polymorphisms Determine the Variability in Human Milk Oligosaccharides.

Frontiers In Nutrition

Lefebvre, Gregory G; Shevlyakova, Maya M; Charpagne, Aline A; Marquis, Julien J; Vogel, Mandy M; Kirsten, Toralf T; Kiess, Wieland W; Austin, Sean S; Sprenger, Norbert N; Binia, Aristea A

Publication Date: 2020

Variant appearance in text: rs3894326

PubMed Link: 33195368

Variant Present in the following documents:

• Main text
• fnut-07-574459.pdf

View BVdb publication page

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Relationship Between Rotavirus P[6] Infection in Korean Neonates and Histo-Blood Group Antigen: a Single-Center Study.

Annals Of Laboratory Medicine

Lee, Su-Kyung SK; Oh, Su Jin SJ; Choi, Seoheui S; Choi, Soo Han SH; Shin, Seon-Hee SH; Lee, Eun Jin EJ; Cho, Eun-Jung EJ; Hyun, Jungwon J; Kim, Hyun Soo HS

Publication Date: 2021-03-01

Variant appearance in text: rs3894326

PubMed Link: 33063679

Variant Present in the following documents:

• Main text
• ALM-41-181.pdf

View BVdb publication page

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Systematic sequence analysis of the FUT3 gene identifies 11 novel alleles in the Sindhi and Punjabi populations from Pakistan.

Scientific Reports

Zhao, Maomao M; Adnan, Atif A; Rakha, Allah A; Nazir, Shahid S; Tian, Meihui M; Zhang, Siyi S; Pang, Hao H

Publication Date: 2020-03-26

Variant appearance in text: rs3894326

PubMed Link: 32218479

Variant Present in the following documents:

• Main text
• 41598_2020_Article_62524.pdf

View BVdb publication page

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Aberrant ABO B Phenotype with Irregular Anti-B Caused by a Para-Bombay FUT1 Mutation.

Transfusion Medicine And Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie

Matzhold, Eva Maria EM; Wagner, Thomas T; Drexler, Camilla C; Schönbacher, Marlies M; Körmöczi, Günther F GF

Publication Date: 2020-02

Variant appearance in text: FUT3: 1067T>A; I356K

PubMed Link: 32110200

Variant Present in the following documents:

• Main text

View BVdb publication page

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Polymorphisms of the TNF Gene and Three Susceptibility Loci Are Associated with Crohn's Disease and Perianal Fistula Crohn's Disease: A Study among the Han Population from South China.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research

Zhang, Min M; Wang, Xiaoyan X; Jiang, Xiaodong X; Yang, Xiangling X; Wen, Chuangyu C; Zhi, Min M; Gao, Xiang X; Hu, Pinjin P; Liu, Huanliang H

Publication Date: 2019-12-17

Variant appearance in text: rs3894326

PubMed Link: 31844038

Variant Present in the following documents:

• Main text

View BVdb publication page

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Human Neonatal Rotavirus Vaccine (RV3-BB) Produces Vaccine Take Irrespective of Histo-Blood Group Antigen Status.

The Journal Of Infectious Diseases

Boniface, Karen K; Byars, Sean G SG; Cowley, Daniel D; Kirkwood, Carl D CD; Bines, Julie E JE

Publication Date: 2020-03-16

Variant appearance in text: rs3894326

PubMed Link: 31763671

Variant Present in the following documents:

• Main text
• jiz333.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: FUT3: 1067T>A; Ile356Lys; rs3894326

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1

View BVdb publication page

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X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.

Scientific Reports

Khan, Muhammad Jaseem MJ; Pollock, Nijole N; Jiang, Huaiyang H; Castro, Carlos C; Nazli, Rubina R; Ahmed, Jawad J; Basit, Sulman S; Rajkovic, Aleksandar A; Yatsenko, Alexander N AN

Publication Date: 2018-11-02

Variant appearance in text: FUT3: I356K; rs3894326

PubMed Link: 30389958

Variant Present in the following documents:

• 41598_2018_34262_MOESM2_ESM.xlsx, sheet 2

View BVdb publication page

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Genomic coordinates and continental distribution of 120 blood group variants reported by the 1000 Genomes Project.

Transfusion

Montemayor-Garcia, Celina C; Karagianni, Panagiota P; Stiles, David A DA; Reese, Erika M EM; Smellie, Danielle A DA; Loy, Debrean A DA; Levy, Kimberly Y KY; Nwokocha, Magdalene M; Bueno, Marina U MU; Miller, Jeffery L JL; Klein, Harvey G HG

Publication Date: 2018-11

Variant appearance in text: FUT3: 1067T>A

PubMed Link: 30312480

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiency.

Annals Of The Rheumatic Diseases

Carapito, Raphael R; Carapito, Christine C; Morlon, Aurore A; Paul, Nicodème N; Vaca Jacome, Alvaro Sebastian AS; Alsaleh, Ghada G; Rolli, Véronique V; Tahar, Ouria O; Aouadi, Ismail I; Rompais, Magali M; Delalande, François F; Pichot, Angélique A; Georgel, Philippe P; Messer, Laurent L; Sibilia, Jean J; Cianferani, Sarah S; Van Dorsselaer, Alain A; Bahram, Seiamak S

Publication Date: 2018-11

Variant appearance in text: FUT3: I356K; rs3894326

PubMed Link: 30030262

Variant Present in the following documents:

• annrheumdis-2018-213524supp002.xlsx, sheet 1

View BVdb publication page

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The Lewis A phenotype is a restriction factor for Rotateq and Rotarix vaccine-take in Nicaraguan children.

Scientific Reports

Bucardo, Filemón F; Nordgren, Johan J; Reyes, Yaoska Y; Gonzalez, Fredman F; Sharma, Sumit S; Svensson, Lennart L

Publication Date: 2018-01-24

Variant appearance in text: rs3894326

PubMed Link: 29367698

Variant Present in the following documents:

• Main text
• 41598_2018_Article_19718.pdf

View BVdb publication page

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Distribution of Lewis and Secretor polymorphisms and corresponding CA19-9 antigen expression in a Chinese population.

Febs Open Bio

Guo, Meng M; Luo, Guopei G; Lu, Renquan R; Shi, Weizhong W; Cheng, He H; Lu, Yu Y; Jin, Kaizhou K; Yang, Chao C; Wang, Zhengshi Z; Long, Jiang J; Xu, Jin J; Ni, Quanxing Q; Liu, Chen C; Yu, Xianjun X

Publication Date: 2017-11

Variant appearance in text: rs3894326

PubMed Link: 29123975

Variant Present in the following documents:

• Main text
• FEB4-7-1660.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: rs3894326

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.

Oncotarget

Raaijmakers, Marieke I G MI; Widmer, Daniel S DS; Narechania, Apurva A; Eichhoff, Ossia O; Freiberger, Sandra N SN; Wenzina, Judith J; Cheng, Phil F PF; Mihic-Probst, Daniela D; Desalle, Rob R; Dummer, Reinhard R; Levesque, Mitchell P MP

Publication Date: 2016-11-22

Variant appearance in text: FUT3: I356K

PubMed Link: 27791198

Variant Present in the following documents:

• oncotarget-07-77163-s003.xlsx, sheet 7
• oncotarget-07-77163-s002.xlsx, sheet 8
• oncotarget-07-77163-s003.xlsx, sheet 8
• oncotarget-07-77163-s003.xlsx, sheet 6
• oncotarget-07-77163-s002.xlsx, sheet 7
• oncotarget-07-77163-s002.xlsx, sheet 3
• oncotarget-07-77163-s002.xlsx, sheet 6
• oncotarget-07-77163-s003.xlsx, sheet 3

View BVdb publication page

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A common genetic variant of fucosyltransferase 2 correlates with serum carcinoembryonic antigen levels and affects cancer screening in patients with primary sclerosing cholangitis.

United European Gastroenterology Journal

Wannhoff, Andreas A; Folseraas, Trine T; Brune, Maik M; Rupp, Christian C; Friedrich, Kilian K; Knierim, Johannes J; Weiss, Karl Heinz KH; Sauer, Peter P; Flechtenmacher, Christa C; Schirmacher, Peter P; Stremmel, Wolfgang W; Hov, Johannes R JR; Gotthardt, Daniel N DN

Publication Date: 2016-02

Variant appearance in text: rs3894326

PubMed Link: 26966527

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of Ulcerative Colitis with FUT2 and FUT3 Polymorphisms in Patients from Southeast China.

Plos One

Hu, Dingyuan D; Zhang, Daguan D; Zheng, Shuzi S; Guo, Maodong M; Lin, Xinxin X; Jiang, Yi Y

Publication Date: 2016

Variant appearance in text: rs3894326

PubMed Link: 26766790

Variant Present in the following documents:

• Main text
• pone.0146557.pdf

View BVdb publication page

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Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One

Holehouse, Alex S AS; Naegle, Kristen M KM

Publication Date: 2015

Variant appearance in text: rs3894326

PubMed Link: 26659599

Variant Present in the following documents:

• pone.0144692.s002.xlsx, sheet 1

View BVdb publication page

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GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics

Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J

Publication Date: 2015-07-25

Variant appearance in text: FUT3: I356K

PubMed Link: 26206375

Variant Present in the following documents:

• 12859_2015_673_MOESM1_ESM.xls, sheet 3

View BVdb publication page

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Blood Groups in Infection and Host Susceptibility.

Clinical Microbiology Reviews

Cooling, Laura L

Publication Date: 2015-07

Variant appearance in text: rs3894326

PubMed Link: 26085552

Variant Present in the following documents:

• Main text

View BVdb publication page

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Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Scientific Reports

Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R

Publication Date: 2015-03-16

Variant appearance in text: FUT3: I356K; rs3894326

PubMed Link: 25773295

Variant Present in the following documents:

• srep09124-s3.xls, sheet 1

View BVdb publication page

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New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nature Communications

Cheng, Ching-Yu CY; Yamashiro, Kenji K; Chen, Li Jia LJ; Ahn, Jeeyun J; Huang, Lulin L; Huang, Lvzhen L; Cheung, Chui Ming G CM; Miyake, Masahiro M; Cackett, Peter D PD; Yeo, Ian Y IY; Laude, Augustinus A; Mathur, Ranjana R; Pang, Junxiong J; Sim, Kar Seng KS; Koh, Adrian H AH; Chen, Peng P; Lee, Shu Yen SY; Wong, Doric D; Chan, Choi Mun CM; Loh, Boon Kwang BK; Sun, Yaoyao Y; Davila, Sonia S; Nakata, Isao I; Nakanishi, Hideo H; Akagi-Kurashige, Yumiko Y; Gotoh, Norimoto N; Tsujikawa, Akitaka A; Matsuda, Fumihiko F; Mori, Keisuke K; Yoneya, Shin S; Sakurada, Yoichi Y; Iijima, Hiroyuki H; Iida, Tomohiro T; Honda, Shigeru S; Lai, Timothy Yuk Yau TY; Tam, Pancy Oi Sin PO; Chen, Haoyu H; Tang, Shibo S; Ding, Xiaoyan X; Wen, Feng F; Lu, Fang F; Zhang, Xiongze X; Shi, Yi Y; Zhao, Peiquan P; Zhao, Bowen B; Sang, Jinghong J; Gong, Bo B; Dorajoo, Rajkumar R; Yuan, Jian-Min JM; Koh, Woon-Puay WP; van Dam, Rob M RM; Friedlander, Yechiel Y; Lin, Ying Y; Hibberd, Martin L ML; Foo, Jia Nee JN; Wang, Ningli N; Wong, Chang Hua CH; Tan, Gavin S GS; Park, Sang Jun SJ; Bhargava, Mayuri M; Gopal, Lingam L; Naing, Thet T; Liao, Jiemin J; Ong, Peng Guan PG; Mitchell, Paul P; Zhou, Peng P; Xie, Xuefeng X; Liang, Jinlong J; Mei, Junpu J; Jin, Xin X; Saw, Seang-Mei SM; Ozaki, Mineo M; Mizoguchi, Takanori T; Kurimoto, Yasuo Y; Woo, Se Joon SJ; Chung, Hum H; Yu, Hyeong-Gon HG; Shin, Joo Young JY; Park, Dong Ho DH; Kim, In Taek IT; Chang, Woohyok W; Sagong, Min M; Lee, Sang-Joon SJ; Kim, Hyun Woong HW; Lee, Ji Eun JE; Li, Yi Y; Liu, Jianjun J; Teo, Yik Ying YY; Heng, Chew Kiat CK; Lim, Tock Han TH; Yang, Suk-Kyun SK; Song, Kyuyoung K; Vithana, Eranga N EN; Aung, Tin T; Bei, Jin Xin JX; Zeng, Yi Xin YX; Tai, E Shyong ES; Li, Xiao Xin XX; Yang, Zhenglin Z; Park, Kyu-Hyung KH; Pang, Chi Pui CP; Yoshimura, Nagahisa N; Wong, Tien Yin TY; Khor, Chiea Chuen CC

Publication Date: 2015-01-28

Variant appearance in text: rs3894326

PubMed Link: 25629512

Variant Present in the following documents:

• Main text
• ncomms7063.pdf

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: FUT3: I356K; rs3894326

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.

Plos One

Taylor-Cousar, Jennifer L JL; Zariwala, Maimoona A MA; Burch, Lauranell H LH; Pace, Rhonda G RG; Drumm, Mitchell L ML; Calloway, Hollin H; Fan, Haiying H; Weston, Brent W BW; Wright, Fred A FA; Knowles, Michael R MR; ,

Publication Date: 2009

Variant appearance in text: rs3894326

PubMed Link: 19169360

Variant Present in the following documents:

• Main text
• pone.0004270.pdf

View BVdb publication page

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