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: rs1800774

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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Characteristics of circulating small noncoding RNAs in plasma and serum during human aging.

Aging Medicine (Milton (N.S.W))

Xiao, Ping P; Shi, Zhangyue Z; Liu, Chenang C; Hagen, Darren E DE

Publication Date: 2023-03

Variant appearance in text: rs1800774

PubMed Link: 36911092

Variant Present in the following documents:

• AGM2-6-35-s002.xlsx, sheet 3

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: rs1800774

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: rs1800774

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

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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: rs1800774

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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A Nutrigenetic Update on CETP Gene-Diet Interactions on Lipid-Related Outcomes.

Current Atherosclerosis Reports

Wuni, Ramatu R; Kuhnle, Gunter G C GGC; Wynn-Jones, Alexandra Azzari AA; Vimaleswaran, Karani Santhanakrishnan KS

Publication Date: 2022-02

Variant appearance in text: rs1800774

PubMed Link: 35098451

Variant Present in the following documents:

• Main text
• 11883_2022_Article_987.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: rs1800774

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

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: CETP: 1215-14C>T; rs1800774

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: CETP: 1215-14C>T; rs1800774

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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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs1800774

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

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c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One

Ganesan, Mala M; Nizamuddin, Sheikh S; Katkam, Shiva Krishna SK; Kumaraswami, Konda K; Hosad, Uday Kumar UK; Lobo, Limmy Loret LL; Kutala, Vijay Kumar VK; Thangaraj, Kumarasamy K

Publication Date: 2016

Variant appearance in text: rs1800774

PubMed Link: 27768712

Variant Present in the following documents:

• Main text
• pone.0164151.pdf

View BVdb publication page

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Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits.

Plos Genetics

Zhang, Futao F; Xie, Dan D; Liang, Meimei M; Xiong, Momiao M

Publication Date: 2016-04

Variant appearance in text: rs1800774

PubMed Link: 27104857

Variant Present in the following documents:

• Main text
• pgen.1005965.pdf

View BVdb publication page

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Cholesteryl ester transfer protein gene polymorphism (I405V) and premature coronary artery disease in an Iranian population.

Bosnian Journal Of Basic Medical Sciences

Goodarzynejad, Hamidreza H; Boroumand, Mohammadali M; Behmanesh, Mehrdad M; Ziaee, Shayan S; Jalali, Arash A

Publication Date: 2016-01-14

Variant appearance in text: rs1800774

PubMed Link: 26773179

Variant Present in the following documents:

• Main text
• BJBMS-16-114.pdf

View BVdb publication page

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Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels.

Metabolism: Clinical And Experimental

Pirim, Dilek D; Wang, Xingbin X; Niemsiri, Vipavee V; Radwan, Zaheda H ZH; Bunker, Clareann H CH; Hokanson, John E JE; Hamman, Richard F RF; Barmada, M Michael MM; Demirci, F Yesim FY; Kamboh, M Ilyas MI

Publication Date: 2016-01

Variant appearance in text: rs1800774

PubMed Link: 26683795

Variant Present in the following documents:

• Main text

View BVdb publication page

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Assessment of established HDL-C loci for association with HDL-C levels and type 2 diabetes in Pima Indians.

Diabetologia

Nair, Anup K AK; Piaggi, Paolo P; McLean, Nellie A NA; Kaur, Manmeet M; Kobes, Sayuko S; Knowler, William C WC; Bogardus, Clifton C; Hanson, Robert L RL; Baier, Leslie J LJ

Publication Date: 2016-03

Variant appearance in text: rs1800774

PubMed Link: 26670163

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: rs1800774

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 1
• mmc3.xlsx, sheet 2

View BVdb publication page

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Evidence from case-control and longitudinal studies supports associations of genetic variation in APOE, CETP, and IL6 with human longevity.

Age (Dordrecht, Netherlands)

Soerensen, Mette M; Dato, Serena S; Tan, Qihua Q; Thinggaard, Mikael M; Kleindorp, Rabea R; Beekman, Marian M; Suchiman, H Eka D HE; Jacobsen, Rune R; McGue, Matt M; Stevnsner, Tinna T; Bohr, Vilhelm A VA; de Craen, Anton J M AJ; Westendorp, Rudi G J RG; Schreiber, Stefan S; Slagboom, P Eline PE; Nebel, Almut A; Vaupel, James W JW; Christensen, Kaare K; Christiansen, Lene L

Publication Date: 2013-04

Variant appearance in text: rs1800774

PubMed Link: 22234866

Variant Present in the following documents:

• Main text

View BVdb publication page

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Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids.

Journal Of Clinical & Experimental Cardiology

Carlquist, John F JF; McKinney, Jason T JT; Horne, Benjamin D BD; Camp, Nicola J NJ; Cannon-Albright, Lisa L; Muhlestein, Joseph B JB; Hopkins, Paul P; Clarke, Jessica L JL; Mower, Chrissa P CP; Park, James J JJ; Nicholas, Zachary P ZP; Huntinghouse, John A JA; Anderson, Jeffrey L JL

Publication Date: 2011-07-10

Variant appearance in text: rs1800774

PubMed Link: 22229114

Variant Present in the following documents:

• Main text

View BVdb publication page

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An assessment of CETP sequence variation in relation to cognitive decline and dementia risk.

International Journal Of Molecular Epidemiology And Genetics

Reynolds, Chandra A CA; Gatz, Margaret M; Pedersen, Nancy L NL; Prince, Jonathan A JA

Publication Date: 2011

Variant appearance in text: rs1800774

PubMed Link: 21686126

Variant Present in the following documents:

• Main text

View BVdb publication page

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes.

Genetic Epidemiology

Li, Yun Y; Willer, Cristen J CJ; Ding, Jun J; Scheet, Paul P; Abecasis, Gonçalo R GR

Publication Date: 2010-12

Variant appearance in text: rs1800774

PubMed Link: 21058334

Variant Present in the following documents:

• Main text

View BVdb publication page

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Cholesterol ester transfer protein, interleukin-8, peroxisome proliferator activator receptor alpha, and Toll-like receptor 4 genetic variations and risk of incident nonfatal myocardial infarction and ischemic stroke.

The American Journal Of Cardiology

Enquobahrie, Daniel A DA; Smith, Nicholas L NL; Bis, Joshua C JC; Carty, Cara L CL; Rice, Kenneth M KM; Lumley, Thomas T; Hindorff, Lucia A LA; Lemaitre, Rozenn N RN; Williams, Michelle A MA; Siscovick, David S DS; Heckbert, Susan R SR; Psaty, Bruce M BM

Publication Date: 2008-06-15

Variant appearance in text: rs1800774

PubMed Link: 18549840

Variant Present in the following documents:

• Main text

View BVdb publication page

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Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels.

Human Genomics

Hinds, David A DA; Seymour, Albert B AB; Durham, L Kathryn LK; Banerjee, Poulabi P; Ballinger, Dennis G DG; Milos, Patrice M PM; Cox, David R DR; Thompson, John F JF; Frazer, Kelly A KA

Publication Date: 2004-11

Variant appearance in text: rs1800774

PubMed Link: 15606997

Variant Present in the following documents:

• Main text
• 1479-7364-1-6-421.pdf

View BVdb publication page

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