Publications:

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Polymorphism in autophagy-related genes LRP1 and CAPZA1 may promote gastric mucosal atrophy.

Genes And Environment : The Official Journal Of The Japanese Environmental Mutagen Society

Yamaguchi, Naoyuki N; Sakaguchi, Takuki T; Isomoto, Hajime H; Inamine, Tatsuo T; Tsukamoto, Ryoya R; Fukuda, Daisuke D; Ohnita, Ken K; Kanda, Tsutomu T; Matsushima, Kayoko K; Hirayama, Tatsuro T; Yashima, Kazuo K; Tsukamoto, Kazuhiro K

Publication Date: 2023-05-17

Variant appearance in text: rs1799986

PubMed Link: 37198664

Variant Present in the following documents:

• Main text
• 41021_2023_Article_274.pdf

View BVdb publication page

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Wnt16 signaling in bone homeostasis and osteoarthristis.

Frontiers In Endocrinology

Ye, Xiaoping X; Liu, Xianwen X

Publication Date: 2022

Variant appearance in text: rs1799986

PubMed Link: 36619549

Variant Present in the following documents:

• Main text
• fendo-13-1095711.pdf

View BVdb publication page

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Exome variants associated with asthma and allergy.

Scientific Reports

Wjst, Matthias M

Publication Date: 2022-12-05

Variant appearance in text: LRP1: 300C>T

PubMed Link: 36470944

Variant Present in the following documents:

• 41598_2022_24960_MOESM1_ESM.pdf

View BVdb publication page

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Pharmacogenetics Role of Genetic Variants in Immune-Related Factors: A Systematic Review Focusing on mCRC.

Pharmaceutics

Scarabel, Lucia L; Bignucolo, Alessia A; Toffoli, Giuseppe G; Cecchin, Erika E; De Mattia, Elena E

Publication Date: 2022-11-15

Variant appearance in text: rs1799986

PubMed Link: 36432658

Variant Present in the following documents:

• Main text
• pharmaceutics-14-02468.pdf

View BVdb publication page

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Immunogenic Cell Death: An Emerging Target in Gastrointestinal Cancers.

Cells

Chiaravalli, Marta M; Spring, Alexia A; Agostini, Antonio A; Piro, Geny G; Carbone, Carmine C; Tortora, Giampaolo G

Publication Date: 2022-09-28

Variant appearance in text: rs1799986

PubMed Link: 36230995

Variant Present in the following documents:

• Main text
• cells-11-03033.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: LRP1: D100D; rs1799986

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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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: LRP1: D100D

PubMed Link: 35311085

Variant Present in the following documents:

• Table_1.xlsx, sheet 4

View BVdb publication page

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Validation of Genetic Markers Associated with Survival in Colorectal Cancer Patients Treated with Oxaliplatin-Based Chemotherapy.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology

Park, Hanla A HA; Seibold, Petra P; Edelmann, Dominic D; Benner, Axel A; Canzian, Federico F; Alwers, Elizabeth E; Jansen, Lina L; Schneider, Martin M; Hoffmeister, Michael M; Brenner, Hermann H; Chang-Claude, Jenny J

Publication Date: 2022-02

Variant appearance in text: rs1799986

PubMed Link: 34862210

Variant Present in the following documents:

• Main text
• 268527_2_supp_7525223_r2sknd.pdf
• 352.pdf

View BVdb publication page

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APOE genotype moderates the relationship between LRP1 polymorphism and cognition across the Alzheimer's disease spectrum via disturbing default mode network.

Cns Neuroscience & Therapeutics

Zang, Feifei F; Zhu, Yao Y; Zhang, Qianqian Q; Tan, Chang C; Wang, Qing Q; Xie, Chunming C; ,

Publication Date: 2021-11

Variant appearance in text: rs1799986

PubMed Link: 34387022

Variant Present in the following documents:

• Main text
• CNS-27-1385.pdf

View BVdb publication page

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Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment.

Behavioural Neurology

Li, Lanlan L; Yang, Yeying Y; Zhang, Qi Q; Wang, Jiao J; Jiang, Jiehui J; Neuroimaging Initiative, Alzheimer's Disease AD

Publication Date: 2021

Variant appearance in text: rs1799986

PubMed Link: 34336000

Variant Present in the following documents:

• Main text
• BN2021-3359103.pdf

View BVdb publication page

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Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications

Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A

Publication Date: 2021-01-08

Variant appearance in text: LRP1: 300C>T; D100D; rs1799986

PubMed Link: 33420045

Variant Present in the following documents:

• 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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Immunogenic cell death pathway polymorphisms for predicting oxaliplatin efficacy in metastatic colorectal cancer.

Journal For Immunotherapy Of Cancer

Arai, Hiroyuki H; Xiao, Yi Y; Loupakis, Fotios F; Kawanishi, Natsuko N; Wang, Jingyuan J; Battaglin, Francesca F; Soni, Shivani S; Zhang, Wu W; Mancao, Christoph C; Salhia, Bodour B; Mumenthaler, Shannon M SM; Weisenberger, Daniel J DJ; Liang, Gangning G; Cremolini, Chiara C; Falcone, Alfredo A; Millstein, Joshua J; Lenz, Heinz-Josef HJ

Publication Date: 2020-11

Variant appearance in text: rs1799986

PubMed Link: 33172883

Variant Present in the following documents:

• Main text
• jitc-2020-001714.pdf

View BVdb publication page

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Association of Low-Density Lipoprotein Receptor-Related Protein 1 and Its rs1799986 Polymorphism With Mild Cognitive Impairment in Chinese Patients With Type 2 Diabetes.

Frontiers In Neuroscience

Cao, Wuyou W; Tian, Sai S; Zhang, Haoqiang H; Zhu, Wenwen W; An, Ke K; Shi, Jijing J; Yuan, Yang Y; Wang, Shaohua S

Publication Date: 2020

Variant appearance in text: rs1799986

PubMed Link: 33013281

Variant Present in the following documents:

• Main text

View BVdb publication page

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Metabolic Health in Obese Subjects-Is There a Link to Lactoferrin and Lactoferrin Receptor-Related Gene Polymorphisms?

Nutrients

Jamka, Małgorzata M; Kaczmarek, Nina N; Mądry, Edyta E; Krzyżanowska-Jankowska, Patrycja P; Bajerska, Joanna J; Kręgielska-Narożna, Matylda M; Bogdański, Paweł P; Walkowiak, Jarosław J

Publication Date: 2020-09-17

Variant appearance in text: rs1799986

PubMed Link: 32957486

Variant Present in the following documents:

• Main text
• nutrients-12-02843.pdf

View BVdb publication page

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Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?

European Journal Of Human Genetics : Ejhg

Ferrari, Luca L; Mangano, Eleonora E; Bonati, Maria Teresa MT; Monterosso, Ilaria I; Capitanio, Daniele D; Chiappori, Federica F; Brambilla, Ilaria I; Gelfi, Cecilia C; Battaglia, Cristina C; Bordoni, Roberta R; Riva, Paola P

Publication Date: 2020-10

Variant appearance in text: LRP1: D100D; rs1799986

PubMed Link: 32514133

Variant Present in the following documents:

• 41431_2020_658_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Genetics of frailty: A longevity perspective.

Translational Research : The Journal Of Laboratory And Clinical Medicine

Sathyan, Sanish S; Verghese, Joe J

Publication Date: 2020-07

Variant appearance in text: rs1799986

PubMed Link: 32289255

Variant Present in the following documents:

• Main text

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: LRP1: D100D; rs1799986

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1

View BVdb publication page

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Variations of Wnt/β-catenin pathway-related genes in susceptibility to knee osteoarthritis: A three-centre case-control study.

Journal Of Cellular And Molecular Medicine

Huang, Yong Y; Jiang, Lifeng L; Yang, Haoyu H; Wu, Lidong L; Xu, Nanwei N; Zhou, Xindie X; Li, Jin J

Publication Date: 2019-12

Variant appearance in text: rs1799986

PubMed Link: 31560818

Variant Present in the following documents:

• Main text
• JCMM-23-8246.pdf

View BVdb publication page

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The neuropathological diagnosis of Alzheimer's disease.

Molecular Neurodegeneration

DeTure, Michael A MA; Dickson, Dennis W DW

Publication Date: 2019-08-02

Variant appearance in text: rs1799986

PubMed Link: 31375134

Variant Present in the following documents:

• Main text
• 13024_2019_Article_333.pdf

View BVdb publication page

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Gender difference and genetic variance in lipoprotein receptor-related protein 1 is associated with mortality.

Biomedical Reports

Alehagen, Urban U; Wågsäter, Dick D

Publication Date: 2019-07

Variant appearance in text: rs1799986

PubMed Link: 31258899

Variant Present in the following documents:

• Main text
• br-11-01-0003.pdf

View BVdb publication page

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Association between LRP1 C766T polymorphism and Alzheimer's disease susceptibility: a meta-analysis.

Scientific Reports

Wang, Yun Y; Liu, Shengyuan S; Wang, Jingjing J; Zhang, Jie J; Hua, Yaqiong Y; Li, Hua H; Tan, Huibiao H; Kuai, Bin B; Wang, Biao B; Sheng, Sitong S

Publication Date: 2017-08-16

Variant appearance in text: rs1799986

PubMed Link: 28814781

Variant Present in the following documents:

• Main text
• 41598_2017_Article_8335.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: rs1799986

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Multiple genetic imaging study of the association between cholesterol metabolism and brain functional alterations in individuals with risk factors for Alzheimer's disease.

Oncotarget

Bai, Feng F; Yuan, Yonggui Y; Shi, Yongmei Y; Zhang, Zhijun Z

Publication Date: 2016-03-29

Variant appearance in text: rs1799986

PubMed Link: 26985771

Variant Present in the following documents:

• Main text
• oncotarget-07-15315.pdf

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: LRP1: D100D; rs1799986

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 3
• mmc3.xlsx, sheet 2
• mmc3.xlsx, sheet 1

View BVdb publication page

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The rs1803274 polymorphism of the BCHE gene is associated with an increased risk of coronary in-stent restenosis.

Bmc Cardiovascular Disorders

Pleva, L L; Kovarova, P P; Faldynova, L L; Plevova, P P; Hilscherova, S S; Zapletalova, J J; Kusnierova, P P; Kukla, P P

Publication Date: 2015-10-24

Variant appearance in text: LRP1: 300C>T; Asp100=; rs1799986

PubMed Link: 26497592

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.

Nature Genetics

Paternoster, Lavinia L; Standl, Marie M; Waage, Johannes J; Baurecht, Hansjörg H; Hotze, Melanie M; Strachan, David P DP; Curtin, John A JA; Bønnelykke, Klaus K; Tian, Chao C; Takahashi, Atsushi A; Esparza-Gordillo, Jorge J; Alves, Alexessander Couto AC; Thyssen, Jacob P JP; den Dekker, Herman T HT; Ferreira, Manuel A MA; Altmaier, Elisabeth E; Sleiman, Patrick Ma PM; Xiao, Feng Li FL; Gonzalez, Juan R JR; Marenholz, Ingo I; Kalb, Birgit B; Yanes, Maria Pino MP; Xu, Cheng-Jian CJ; Carstensen, Lisbeth L; Groen-Blokhuis, Maria M MM; Venturini, Cristina C; Pennell, Craig E CE; Barton, Sheila J SJ; Levin, Albert M AM; Curjuric, Ivan I; Bustamante, Mariona M; Kreiner-Møller, Eskil E; Lockett, Gabrielle A GA; Bacelis, Jonas J; Bunyavanich, Supinda S; Myers, Rachel A RA; Matanovic, Anja A; Kumar, Ashish A; Tung, Joyce Y JY; Hirota, Tomomitsu T; Kubo, Michiaki M; McArdle, Wendy L WL; Henderson, A J AJ; Kemp, John P JP; Zheng, Jie J; Smith, George Davey GD; Rüschendorf, Franz F; Bauerfeind, Anja A; Lee-Kirsch, Min Ae MA; Arnold, Andreas A; Homuth, Georg G; Schmidt, Carsten O CO; Mangold, Elisabeth E; Cichon, Sven S; Keil, Thomas T; Rodríguez, Elke E; Peters, Annette A; Franke, Andre A; Lieb, Wolfgang W; Novak, Natalija N; Fölster-Holst, Regina R; Horikoshi, Momoko M; Pekkanen, Juha J; Sebert, Sylvain S; Husemoen, Lise L LL; Grarup, Niels N; de Jongste, Johan C JC; Rivadeneira, Fernando F; Hofman, Albert A; Jaddoe, Vincent Wv VW; Pasmans, Suzanne Gma SG; Elbert, Niels J NJ; Uitterlinden, André G AG; Marks, Guy B GB; Thompson, Philip J PJ; Matheson, Melanie C MC; Robertson, Colin F CF; , ; Ried, Janina S JS; Li, Jin J; Zuo, Xian Bo XB; Zheng, Xiao Dong XD; Yin, Xian Yong XY; Sun, Liang Dan LD; McAleer, Maeve A MA; O'Regan, Grainne M GM; Fahy, Caoimhe Mr CM; Campbell, Linda E LE; Macek, Milan M; Kurek, Michael M; Hu, Donglei D; Eng, Celeste C; Postma, Dirkje S DS; Feenstra, Bjarke B; Geller, Frank F; Hottenga, Jouke Jan JJ; Middeldorp, Christel M CM; Hysi, Pirro P; Bataille, Veronique V; Spector, Tim T; Tiesler, Carla Mt CM; Thiering, Elisabeth E; Pahukasahasram, Badri B; Yang, James J JJ; Imboden, Medea M; Huntsman, Scott S; Vilor-Tejedor, Natàlia N; Relton, Caroline L CL; Myhre, Ronny R; Nystad, Wenche W; Custovic, Adnan A; Weiss, Scott T ST; Meyers, Deborah A DA; Söderhäll, Cilla C; Melén, Erik E; Ober, Carole C; Raby, Benjamin A BA; Simpson, Angela A; Jacobsson, Bo B; Holloway, John W JW; Bisgaard, Hans H; Sunyer, Jordi J; Hensch, Nicole M Probst NMP; Williams, L Keoki LK; Godfrey, Keith M KM; Wang, Carol A CA; Boomsma, Dorret I DI; Melbye, Mads M; Koppelman, Gerard H GH; Jarvis, Deborah D; McLean, Wh Irwin WI; Irvine, Alan D AD; Zhang, Xue Jun XJ; Hakonarson, Hakon H; Gieger, Christian C; Burchard, Esteban G EG; Martin, Nicholas G NG; Duijts, Liesbeth L; Linneberg, Allan A; Jarvelin, Marjo-Riitta MR; Noethen, Markus M MM; Lau, Susanne S; Hübner, Norbert N; Lee, Young-Ae YA; Tamari, Mayumi M; Hinds, David A DA; Glass, Daniel D; Brown, Sara J SJ; Heinrich, Joachim J; Evans, David M DM; Weidinger, Stephan S

Publication Date: 2015-12

Variant appearance in text: rs1799986

PubMed Link: 26482879

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variant of Interleukin-18 gene is associated with the Frailty Index in the English Longitudinal Study of Ageing.

Age And Ageing

Mekli, Krisztina K; Marshall, Alan A; Nazroo, James J; Vanhoutte, Bram B; Pendleton, Neil N

Publication Date: 2015-11

Variant appearance in text: rs1799986

PubMed Link: 26396182

Variant Present in the following documents:

• Main text
• afv122.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: LRP1: D100D; rs1799986

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

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: LRP1: D100D; rs1799986

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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LRP-1 polymorphism is associated with global and regional amyloid load in Alzheimer's Disease in humans in-vivo.

Neuroimage. Clinical

Grimmer, Timo T; Goldhardt, Oliver O; Guo, Liang-Hao LH; Yousefi, Behrooz H BH; Förster, Stefan S; Drzezga, Alexander A; Sorg, Christian C; Alexopoulos, Panagiotis P; Förstl, Hans H; Kurz, Alexander A; Perneczky, Robert R

Publication Date: 2014

Variant appearance in text: rs1799986

PubMed Link: 24596678

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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The association between LRP-1 variants and chylomicron uptake after a high fat meal.

Nutrition, Metabolism, And Cardiovascular Diseases : Nmcd

Frazier-Wood, A C AC; Kabagambe, E K EK; Wojczynski, M K MK; Borecki, I B IB; Tiwari, H K HK; Smith, C E CE; Ordovas, J M JM; Arnett, D K DK

Publication Date: 2013-11

Variant appearance in text: rs1799986

PubMed Link: 23484911

Variant Present in the following documents:

• Main text

View BVdb publication page

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Low-density lipoprotein receptor-related protein 1 variant interacts with saturated fatty acids in Puerto Ricans.

Obesity (Silver Spring, Md.)

Smith, Caren E CE; Tucker, Katherine L KL; Lee, Yu-Chi YC; Lai, Chao-Qiang CQ; Parnell, Laurence D LD; Ordovás, José M JM

Publication Date: 2013-03

Variant appearance in text: rs1799986

PubMed Link: 23404896

Variant Present in the following documents:

• Main text

View BVdb publication page

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Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies.

International Journal Of Obesity (2005)

Smith, C E CE; Ngwa, J J; Tanaka, T T; Qi, Q Q; Wojczynski, M K MK; Lemaitre, R N RN; Anderson, J S JS; Manichaikul, A A; Mikkilä, V V; van Rooij, F J A FJ; Ye, Z Z; Bandinelli, S S; Frazier-Wood, A C AC; Houston, D K DK; Hu, F F; Langenberg, C C; McKeown, N M NM; Mozaffarian, D D; North, K E KE; Viikari, J J; Zillikens, M C MC; Djoussé, L L; Hofman, A A; Kähönen, M M; Kabagambe, E K EK; Loos, R J F RJ; Saylor, G B GB; Forouhi, N G NG; Liu, Y Y; Mukamal, K J KJ; Chen, Y-D I YD; Tsai, M Y MY; Uitterlinden, A G AG; Raitakari, O O; van Duijn, C M CM; Arnett, D K DK; Borecki, I B IB; Cupples, L A LA; Ferrucci, L L; Kritchevsky, S B SB; Lehtimäki, T T; Qi, Lu L; Rotter, J I JI; Siscovick, D S DS; Wareham, N J NJ; Witteman, J C M JC; Ordovás, J M JM; Nettleton, J A JA

Publication Date: 2013-09

Variant appearance in text: rs1799986

PubMed Link: 23357958

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association study of candidate gene polymorphisms with amnestic mild cognitive impairment in a Chinese population.

Plos One

Liu, Xiaoyan X; Yue, Chunxian C; Xu, Zhi Z; Shu, Hao H; Pu, Mengjia M; Yu, Hui H; Shi, Yongmei Y; Zhuang, Liying L; Xu, Xiaohui X; Zhang, Zhijun Z

Publication Date: 2012

Variant appearance in text: rs1799986

PubMed Link: 22911757

Variant Present in the following documents:

• Main text
• pone.0041198.pdf

View BVdb publication page

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Preliminary evidence for an association between LRP-1 genotype and body mass index in humans.

Plos One

Frazier-Wood, Alexis C AC; Kabagambe, Edmond K EK; Borecki, Ingrid B IB; Tiwari, Hemant K HK; Ordovas, Jose M JM; Arnett, Donna K DK

Publication Date: 2012

Variant appearance in text: rs1799986

PubMed Link: 22347399

Variant Present in the following documents:

• Main text
• pone.0030732.pdf

View BVdb publication page

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Dyslipidemia and dementia: current epidemiology, genetic evidence, and mechanisms behind the associations.

Journal Of Alzheimer'S Disease : Jad

Reitz, Christiane C

Publication Date: 2012

Variant appearance in text: rs1799986

PubMed Link: 21965313

Variant Present in the following documents:

• Main text

View BVdb publication page

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LRP-1 variation is not associated with risk of Alzheimer's disease.

International Journal Of Molecular Epidemiology And Genetics

Chalmers, Katy A KA; Barker, Rachel R; Passmore, Peter A PA; Panza, Francesco F; Seripa, Davide D; Solfrizzi, Vincenzo V; Love, Seth S; Prince, Jonathan A JA; Kehoe, Patrick G PG

Publication Date: 2010-02-20

Variant appearance in text: rs1799986

PubMed Link: 21537384

Variant Present in the following documents:

• Main text

View BVdb publication page

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Causes versus effects: the increasing complexities of Alzheimer's disease pathogenesis.

Expert Review Of Neurotherapeutics

Mondragón-Rodríguez, Siddhartha S; Basurto-Islas, Gustavo G; Lee, Hyoung-gon HG; Perry, George G; Zhu, Xiongwei X; Castellani, Rudy J RJ; Smith, Mark A MA

Publication Date: 2010-05

Variant appearance in text: rs1799986

PubMed Link: 20420489

Variant Present in the following documents:

• Main text

View BVdb publication page

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Disparities in allele frequencies and population differentiation for 101 disease-associated single nucleotide polymorphisms between Puerto Ricans and non-Hispanic whites.

Bmc Genetics

Mattei, Josiemer J; Parnell, Laurence D LD; Lai, Chao-Qiang CQ; Garcia-Bailo, Bibiana B; Adiconis, Xian X; Shen, Jian J; Arnett, Donna D; Demissie, Serkalem S; Tucker, Katherine L KL; Ordovas, Jose M JM

Publication Date: 2009-08-14

Variant appearance in text: rs1799986

PubMed Link: 19682384

Variant Present in the following documents:

View BVdb publication page

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An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Edwards, Todd L TL; Pericak-Vance, Margaret M; Gilbert, Johnny R JR; Haines, Jonathan L JL; Martin, Eden R ER; Ritchie, Marylyn D MD

Publication Date: 2009-07-05

Variant appearance in text: rs1799986

PubMed Link: 19105203

Variant Present in the following documents:

• Main text

View BVdb publication page

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Evaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's disease.

American Journal Of Epidemiology

Kavvoura, Fotini K FK; McQueen, Matthew B MB; Khoury, Muin J MJ; Tanzi, Rudolph E RE; Bertram, Lars L; Ioannidis, John P A JP

Publication Date: 2008-10-15

Variant appearance in text: rs1799986

PubMed Link: 18779388

Variant Present in the following documents:

• Main text

View BVdb publication page

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Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease.

Proceedings Of The National Academy Of Sciences Of The United States Of America

De Ferrari, Giancarlo V GV; Papassotiropoulos, Andreas A; Biechele, Travis T; Wavrant De-Vrieze, Fabienne F; Avila, Miguel E ME; Major, Michael B MB; Myers, Amanda A; Sáez, Katia K; Henríquez, Juan P JP; Zhao, Alice A; Wollmer, M Axel MA; Nitsch, Roger M RM; Hock, Christoph C; Morris, Chris M CM; Hardy, John J; Moon, Randall T RT

Publication Date: 2007-05-29

Variant appearance in text: rs1799986

PubMed Link: 17517621

Variant Present in the following documents:

• Main text

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