Publications:

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Circulating messenger RNA variants as a potential biomarker for surveillance of hepatocellular carcinoma.

Frontiers In Oncology

Block, Timothy T; Zezulinski, Daniel D; Kaplan, David E DE; Lu, Jingqiao J; Zanine, Samantha S; Zhan, Tingting T; Doria, Cataldo C; Sayeed, Aejaz A

Publication Date: 2022

Variant appearance in text: rs675

PubMed Link: 36582804

Variant Present in the following documents:

• Table_6.xlsx, sheet 1

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Genetic Factors Associated with Response to Vitamin E Treatment in NAFLD.

Antioxidants (Basel, Switzerland)

Civelek, Mehtap M; Podszun, Maren C MC

Publication Date: 2022-06-28

Variant appearance in text: rs675

PubMed Link: 35883775

Variant Present in the following documents:

• Main text
• antioxidants-11-01284.pdf

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[Nutrigenetics: potentials and applications in cardiovascular diseases and associated risk factors].

Revista De La Facultad De Ciencias Medicas (Cordoba, Argentina)

Defagó, Maria Daniela MD; Eynard, Aldo Renato AR

Publication Date: 2022-06-06

Variant appearance in text: rs675

PubMed Link: 35700474

Variant Present in the following documents:

• 1853-0605-79-2-168.pdf

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Integrated molecular profiling of patient-derived ovarian cancer models identifies clinically relevant signatures and tumor vulnerabilities.

International Journal Of Cancer

Lupia, Michela M; Melocchi, Valentina V; Bizzaro, Francesca F; Lo Riso, Pietro P; Dama, Elisa E; Baronio, Micol M; Ranghiero, Alberto A; Barberis, Massimo M; Bernard, Loris L; Bertalot, Giovanni G; Giavazzi, Raffaella R; Testa, Giuseppe G; Bianchi, Fabrizio F; Cavallaro, Ugo U

Publication Date: 2022-07-15

Variant appearance in text: APOA4: Thr367Ala; rs675

PubMed Link: 35218560

Variant Present in the following documents:

• IJC-151-240-s001.xlsx, sheet 7

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Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies.

Cancer Gene Therapy

Denisova, Evgeniya E; Westphal, Dana D; Surowy, Harald M HM; Meier, Friedegund F; Hutter, Barbara B; Reifenberger, Julia J; Rütten, Arno A; Schulz, Alexander A; Sergon, Mildred M; Ziemer, Mirjana M; Brors, Benedikt B; Betz, Regina C RC; Redler, Silke S

Publication Date: 2022-06

Variant appearance in text: APOA4: T367A

PubMed Link: 34045664

Variant Present in the following documents:

• 41417_2021_347_MOESM4_ESM.xls, sheet 14

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A Population-Specific Major Allele Reference Genome From The United Arab Emirates Population.

Frontiers In Genetics

Daw Elbait, Gihan G; Henschel, Andreas A; Tay, Guan K GK; Al Safar, Habiba S HS

Publication Date: 2021

Variant appearance in text: rs675

PubMed Link: 33968136

Variant Present in the following documents:

• Main text

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Genetic variants for personalised management of very low carbohydrate ketogenic diets.

Bmj Nutrition, Prevention & Health

Aronica, Lucia L; Volek, Jeff J; Poff, Angela A; D'agostino, Dominic P DP

Publication Date: 2020-12

Variant appearance in text: rs675

PubMed Link: 33521546

Variant Present in the following documents:

• Main text
• bmjnph-2020-000167.pdf

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Genetic Variants Shaping Inter-individual Differences in Response to Dietary Intakes-A Narrative Review of the Case of Vitamins.

Frontiers In Nutrition

Niforou, Aikaterini A; Konstantinidou, Valentini V; Naska, Androniki A

Publication Date: 2020

Variant appearance in text: rs675

PubMed Link: 33335908

Variant Present in the following documents:

• Main text
• fnut-07-558598.pdf

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Influence of genetic polymorphisms in homocysteine and lipid metabolism systems on antidepressant drug response.

Bmc Psychiatry

Yuan, Baoyu B; Sun, Xiaoyan X; Xu, Zhi Z; Pu, Mengjia M; Yuan, Yonggui Y; Zhang, Zhijun Z

Publication Date: 2020-08-14

Variant appearance in text: rs675

PubMed Link: 32795354

Variant Present in the following documents:

• Main text
• 12888_2020_Article_2798.pdf

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Stress proteins: the biological functions in virus infection, present and challenges for target-based antiviral drug development.

Signal Transduction And Targeted Therapy

Wan, Qianya Q; Song, Dan D; Li, Huangcan H; He, Ming-Liang ML

Publication Date: 2020-07-13

Variant appearance in text: rs675

PubMed Link: 32661235

Variant Present in the following documents:

• 41392_2020_Article_233.pdf

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In-depth plasma proteomics reveals increase in circulating PD-1 during anti-PD-1 immunotherapy in patients with metastatic cutaneous melanoma.

Journal For Immunotherapy Of Cancer

Babačić, Haris H; Lehtiö, Janne J; Pico de Coaña, Yago Y; Pernemalm, Maria M; Eriksson, Hanna H

Publication Date: 2020-05

Variant appearance in text: rs675

PubMed Link: 32457125

Variant Present in the following documents:

• jitc-2019-000204supp003.xlsx, sheet 3

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Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.

Bmc Medical Genomics

Dron, Jacqueline S JS; Wang, Jian J; McIntyre, Adam D AD; Iacocca, Michael A MA; Robinson, John F JF; Ban, Matthew R MR; Cao, Henian H; Hegele, Robert A RA

Publication Date: 2020-02-10

Variant appearance in text: APOA4: 1099A>G; Thr367Ala

PubMed Link: 32041611

Variant Present in the following documents:

• 12920_2020_669_MOESM1_ESM.xlsx, sheet 3

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: rs675

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3

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Frequency and phenotype consequence of APOC3 rare variants in patients with very low triglyceride levels.

Bmc Medical Genomics

Crawford, Dana C DC; Restrepo, Nicole A NA; Diggins, Kirsten E KE; Farber-Eger, Eric E; Wells, Quinn S QS

Publication Date: 2018-09-14

Variant appearance in text: rs675

PubMed Link: 30255797

Variant Present in the following documents:

• Main text
• 12920_2018_Article_387.pdf

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Association of serum lipids and coronary artery disease with polymorphisms in the apolipoprotein AI-CIII-AIV gene cluster.

Cogent Medicine

Rai, Himanshu H; Sinha, Nakul N; Finn, James J; Agrawal, Suraksha S; Mastana, Sarabjit S

Publication Date: 2016-12-31

Variant appearance in text: rs675

PubMed Link: 28261635

Variant Present in the following documents:

• Main text
• oamd-3-1266789.pdf

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Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer.

Scientific Reports

Feliubadaló, Lídia L; Tonda, Raúl R; Gausachs, Mireia M; Trotta, Jean-Rémi JR; Castellanos, Elisabeth E; López-Doriga, Adriana A; Teulé, Àlex À; Tornero, Eva E; Del Valle, Jesús J; Gel, Bernat B; Gut, Marta M; Pineda, Marta M; González, Sara S; Menéndez, Mireia M; Navarro, Matilde M; Capellá, Gabriel G; Gut, Ivo I; Serra, Eduard E; Brunet, Joan J; Beltran, Sergi S; Lázaro, Conxi C

Publication Date: 2017-01-04

Variant appearance in text: APOA4: 1099A>G; Thr367Ala

PubMed Link: 28050010

Variant Present in the following documents:

• srep37984-s2.xls, sheet 1

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A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.

Human Molecular Genetics

Lamina, Claudia C; Friedel, Salome S; Coassin, Stefan S; Rueedi, Rico R; Yousri, Noha A NA; Seppälä, Ilkka I; Gieger, Christian C; Schönherr, Sebastian S; Forer, Lukas L; Erhart, Gertraud G; Kollerits, Barbara B; Marques-Vidal, Pedro P; Ried, Janina J; Waeber, Gerard G; Bergmann, Sven S; Dähnhardt, Doreen D; Stöckl, Andrea A; Kiechl, Stefan S; Raitakari, Olli T OT; Kähönen, Mika M; Willeit, Johann J; Kedenko, Ludmilla L; Paulweber, Bernhard B; Peters, Annette A; Meitinger, Thomas T; Strauch, Konstantin K; , ; Lehtimäki, Terho T; Hunt, Steven C SC; Vollenweider, Peter P; Kronenberg, Florian F

Publication Date: 2016-08-15

Variant appearance in text: rs675

PubMed Link: 27412012

Variant Present in the following documents:

• Main text
• supp_ddw211_GWA_apoA4_Supplement_Final.pdf
• ddw211.pdf

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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: rs675

PubMed Link: 26659599

Variant Present in the following documents:

• pone.0144692.s002.xlsx, sheet 1

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Gene polymorphisms and gene scores linked to low serum carotenoid status and their associations with metabolic disturbance and depressive symptoms in African-American adults.

The British Journal Of Nutrition

Beydoun, May A MA; Nalls, Michael A MA; Canas, J Atilio JA; Evans, Michele K MK; Zonderman, Alan B AB

Publication Date: 2014-09-28

Variant appearance in text: rs675

PubMed Link: 25201307

Variant Present in the following documents:

• Main text

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A probabilistic model to predict clinical phenotypic traits from genome sequencing.

Plos Computational Biology

Chen, Yun-Ching YC; Douville, Christopher C; Wang, Cheng C; Niknafs, Noushin N; Yeo, Grace G; Beleva-Guthrie, Violeta V; Carter, Hannah H; Stenson, Peter D PD; Cooper, David N DN; Li, Biao B; Mooney, Sean S; Karchin, Rachel R

Publication Date: 2014-09

Variant appearance in text: APOA4: T367A

PubMed Link: 25188385

Variant Present in the following documents:

• pcbi.1003825.s014.xlsx, sheet 1

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Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.

Nature Communications

Ko, Arthur A; Cantor, Rita M RM; Weissglas-Volkov, Daphna D; Nikkola, Elina E; Reddy, Prasad M V Linga PM; Sinsheimer, Janet S JS; Pasaniuc, Bogdan B; Brown, Robert R; Alvarez, Marcus M; Rodriguez, Alejandra A; Rodriguez-Guillen, Rosario R; Bautista, Ivette C IC; Arellano-Campos, Olimpia O; Muñoz-Hernández, Linda L LL; Salomaa, Veikko V; Kaprio, Jaakko J; Jula, Antti A; Jauhiainen, Matti M; Heliövaara, Markku M; Raitakari, Olli O; Lehtimäki, Terho T; Eriksson, Johan G JG; Perola, Markus M; Lohmueller, Kirk E KE; Matikainen, Niina N; Taskinen, Marja-Riitta MR; Rodriguez-Torres, Maribel M; Riba, Laura L; Tusie-Luna, Teresa T; Aguilar-Salinas, Carlos A CA; Pajukanta, Päivi P

Publication Date: 2014-06-02

Variant appearance in text: rs675

PubMed Link: 24886709

Variant Present in the following documents:

• ncomms4983.pdf

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Central obesity in males affected by a dyslipidemia-associated genetic polymorphism on APOA1/C3/A4/A5 gene cluster.

Nutrition & Diabetes

Hsu, M-C MC; Chang, C-S CS; Lee, K-T KT; Sun, H-Y HY; Tsai, Y-S YS; Kuo, P-H PH; Young, K-C KC; Wu, C-H CH

Publication Date: 2013-03-04

Variant appearance in text: rs675

PubMed Link: 23459084

Variant Present in the following documents:

• Main text
• nutd20132a.pdf

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Association of gene variants with lipid levels in response to fenofibrate is influenced by metabolic syndrome status.

Atherosclerosis

Feitosa, Mary F MF; An, Ping P; Ordovas, Jose M JM; Ketkar, Shamika S; Hopkins, Paul N PN; Straka, Robert J RJ; Arnett, Donna K DK; Borecki, Ingrid B IB

Publication Date: 2011-04

Variant appearance in text: rs675

PubMed Link: 21324458

Variant Present in the following documents:

• Main text

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The APOA1/C3/A4/A5 cluster and markers of allostatic load in the Boston Puerto Rican Health Study.

Nutrition, Metabolism, And Cardiovascular Diseases : Nmcd

Mattei, J J; Demissie, S S; Tucker, K L KL; Ordovas, J M JM

Publication Date: 2011-11

Variant appearance in text: rs675

PubMed Link: 20674306

Variant Present in the following documents:

• Main text

View BVdb publication page

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APOE, CETP and LPL genes show strong association with lipid levels in Greek children.

Nutrition, Metabolism, And Cardiovascular Diseases : Nmcd

Smart, M C MC; Dedoussis, G G; Louizou, E E; Yannakoulia, M M; Drenos, F F; Papoutsakis, C C; Maniatis, N N; Humphries, S E SE; Talmud, P J PJ

Publication Date: 2010-01

Variant appearance in text: rs675

PubMed Link: 19403283

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: rs675

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: rs675

PubMed Link: 19131662

Variant Present in the following documents:

• Main text

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Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study.

Pharmacogenetics And Genomics

Liu, Yongjun Y; Ordovas, Jose M JM; Gao, Guimin G; Province, Michael M; Straka, Robert J RJ; Tsai, Michael Y MY; Lai, Chao-Qiang CQ; Zhang, Kui K; Borecki, Ingrid I; Hixson, James E JE; Allison, David B DB; Arnett, Donna K DK

Publication Date: 2009-02

Variant appearance in text: rs675

PubMed Link: 19057464

Variant Present in the following documents:

• Main text

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Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

Experimental Gerontology

Boes, Eva E; Coassin, Stefan S; Kollerits, Barbara B; Heid, Iris M IM; Kronenberg, Florian F

Publication Date: 2009-03

Variant appearance in text: rs675

PubMed Link: 19041386

Variant Present in the following documents:

• Main text

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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: rs675

PubMed Link: 18513389

Variant Present in the following documents:

• Main text

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A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.

Bmc Genetics

Sebastiani, Paola P; Zhao, Zhenming Z; Abad-Grau, Maria M MM; Riva, Alberto A; Hartley, Stephen W SW; Sedgewick, Amanda E AE; Doria, Alessandro A; Montano, Monty M; Melista, Efthymia E; Terry, Dellara D; Perls, Thomas T TT; Steinberg, Martin H MH; Baldwin, Clinton T CT

Publication Date: 2008-01-14

Variant appearance in text: rs675

PubMed Link: 18194558

Variant Present in the following documents:

• Main text

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Polymorphism in maternal LRP8 gene is associated with fetal growth.

American Journal Of Human Genetics

Wang, Lin L; Wang, Xiaobin X; Laird, Nan N; Zuckerman, Barry B; Stubblefield, Philip P; Xu, Xin X

Publication Date: 2006-05

Variant appearance in text: rs675

PubMed Link: 16642433

Variant Present in the following documents:

• Main text

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Lipoprotein genotype and conserved pathway for exceptional longevity in humans.

Plos Biology

Atzmon, Gil G; Rincon, Marielisa M; Schechter, Clyde B CB; Shuldiner, Alan R AR; Lipton, Richard B RB; Bergman, Aviv A; Barzilai, Nir N

Publication Date: 2006-04

Variant appearance in text: rs675

PubMed Link: 16602826

Variant Present in the following documents:

• Main text
• pbio.0040113.pdf

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Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11.

Genomics

Olivier, Michael M; Wang, Xujing X; Cole, Regina R; Gau, Brian B; Kim, Jessica J; Rubin, Edward M EM; Pennacchio, Len A LA

Publication Date: 2004-05

Variant appearance in text: rs675

PubMed Link: 15081120

Variant Present in the following documents:

• Main text

View BVdb publication page

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