Publications:

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Identifying genetic variants for amyloid β in subcortical vascular cognitive impairment.

Frontiers In Aging Neuroscience

Kim, Hang-Rai HR; Jung, Sang-Hyuk SH; Kim, Beomsu B; Kim, Jaeho J; Jang, Hyemin H; Kim, Jun Pyo JP; Kim, So Yeon SY; Na, Duk L DL; Kim, Hee Jin HJ; Nho, Kwangsik K; Won, Hong-Hee HH; Seo, Sang Won SW

Publication Date: 2023

Variant appearance in text: rs6859

PubMed Link: 37143691

Variant Present in the following documents:

• fnagi-15-1160536.pdf

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Metabolic Overlap between Alzheimer's Disease and Metabolic Syndrome Identifies the PVRL2 Gene as a New Modulator of Diabetic Dyslipidemia.

International Journal Of Molecular Sciences

Guardiola, Montse M; Muntané, Gerard G; Martínez, Iris I; Martorell, Lourdes L; Girona, Josefa J; Ibarretxe, Daiana D; Plana, Núria N; Bullido, María J MJ; Vilella, Elisabet E; Ribalta, Josep J

Publication Date: 2023-04-18

Variant appearance in text: rs6859

PubMed Link: 37108578

Variant Present in the following documents:

• Main text
• ijms-24-07415.pdf

View BVdb publication page

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Deep learning-based polygenic risk analysis for Alzheimer's disease prediction.

Communications Medicine

Zhou, Xiaopu X; Chen, Yu Y; Ip, Fanny C F FCF; Jiang, Yuanbing Y; Cao, Han H; Lv, Ge G; Zhong, Huan H; Chen, Jiahang J; Ye, Tao T; Chen, Yuewen Y; Zhang, Yulin Y; Ma, Shuangshuang S; Lo, Ronnie M N RMN; Tong, Estella P S EPS; , ; Mok, Vincent C T VCT; Kwok, Timothy C Y TCY; Guo, Qihao Q; Mok, Kin Y KY; Shoai, Maryam M; Hardy, John J; Chen, Lei L; Fu, Amy K Y AKY; Ip, Nancy Y NY

Publication Date: 2023-04-06

Variant appearance in text: rs6859

PubMed Link: 37024668

Variant Present in the following documents:

• Main text
• 43856_2023_Article_269.pdf

View BVdb publication page

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N6-methyladenosine (m6A) RNA modification in the pathophysiology of heart failure: a narrative review.

Cardiovascular Diagnosis And Therapy

Liu, Sihan S; Wang, Tongyu T; Cheng, Zeyi Z; Liu, Jing J

Publication Date: 2022-12

Variant appearance in text: rs6859

PubMed Link: 36605077

Variant Present in the following documents:

• Main text
• cdt-12-06-908.pdf

View BVdb publication page

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RNA methylation in vascular disease: a systematic review.

Journal Of Cardiothoracic Surgery

Shu, Yue Y; Guo, Yilong Y; Zheng, Yin Y; He, Shuwu S; Shi, Zhensu Z

Publication Date: 2022-12-19

Variant appearance in text: rs6859

PubMed Link: 36536469

Variant Present in the following documents:

• Main text
• 13019_2022_Article_2077.pdf

View BVdb publication page

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Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research

Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C

Publication Date: 2022-10-21

Variant appearance in text: NECTIN2: 1043-3434A>G; rs6859

PubMed Link: 36269797

Variant Present in the following documents:

• ccr-22-2060_supplementary_table_s5_suppts5.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: rs6859

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_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: rs6859

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

View BVdb publication page

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Inter- and intra-chromosomal modulators of the APOE ɛ2 and ɛ4 effects on the Alzheimer's disease risk.

Geroscience

Nazarian, Alireza A; Philipp, Ian I; Culminskaya, Irina I; He, Liang L; Kulminski, Alexander M AM

Publication Date: 2022-07-09

Variant appearance in text: rs6859

PubMed Link: 35809216

Variant Present in the following documents:

• Main text
• 11357_2022_Article_617.pdf

View BVdb publication page

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The Relationship Between Low-Density Lipoprotein Cholesterol and Progression of Mild Cognitive Impairment: The Influence of rs6859 in PVRL2.

Frontiers In Genetics

Xiao, Qianyi Q; Xi, Jianxiong J; Wang, Ruru R; Zhao, Qianhua Q; Liang, Xiaoniu X; Wu, Wanqing W; Zheng, Li L; Guo, Qihao Q; Hong, Zhen Z; Fu, Hua H; Ding, Ding D

Publication Date: 2022

Variant appearance in text: rs6859

PubMed Link: 35273639

Variant Present in the following documents:

• Main text
• fgene-13-823406.pdf

View BVdb publication page

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Evaluation of mild cognitive impairment genetic susceptibility risks in a Chinese population.

Bmc Psychiatry

Zhang, Yelei Y; Li, Xiaoyue X; Hu, Yu Y; Yuan, Hongwei H; Wu, Xiaodong X; Yang, Yating Y; Zhao, Tongtong T; Hu, Ke K; Wang, Zhiqiang Z; Wang, Guoqiang G; Zhang, Kai K; Liu, Huanzhong H

Publication Date: 2022-02-08

Variant appearance in text: rs6859

PubMed Link: 35135506

Variant Present in the following documents:

• Main text
• 12888_2022_Article_3756.pdf

View BVdb publication page

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Evaluation of mild cognitive impairment genetic susceptibility risks in a Chinese population.

Bmc Psychiatry

Zhang, Yelei Y; Li, Xiaoyue X; Hu, Yu Y; Yuan, Hongwei H; Wu, Xiaodong X; Yang, Yating Y; Zhao, Tongtong T; Hu, Ke K; Wang, Zhiqiang Z; Wang, Guoqiang G; Zhang, Kai K; Liu, Huanzhong H

Publication Date: 2022-02-08

Variant appearance in text: rs6859

PubMed Link: 35135506

Variant Present in the following documents:

• Main text
• 12888_2022_Article_3756.pdf

View BVdb publication page

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Association of Gene Polymorphisms in APOE and BIN1 With Dementia of Alzheimer's Type Susceptibility in Chinese Han Population.

Frontiers In Psychiatry

Li, Xiaoyue X; Zhang, Yelei Y; Chen, Xinyu X; Yuan, Hongwei H; Wang, Zhiqiang Z; Wang, Guoqiang G; Zhang, Kai K; Liu, Huanzhong H

Publication Date: 2021

Variant appearance in text: rs6859

PubMed Link: 34733192

Variant Present in the following documents:

• Main text
• fpsyt-12-753909.pdf

View BVdb publication page

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Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population.

Genes

Bocharova, Anna A; Vagaitseva, Kseniya K; Marusin, Andrey A; Zhukova, Natalia N; Zhukova, Irina I; Minaycheva, Larisa L; Makeeva, Oksana O; Stepanov, Vadim V

Publication Date: 2021-10-19

Variant appearance in text: rs6859

PubMed Link: 34681041

Variant Present in the following documents:

• Main text
• genes-12-01647.pdf

View BVdb publication page

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Dissection of the genetic basis of genotype-by-environment interactions for grain yield and main agronomic traits in Iranian bread wheat landraces and cultivars.

Scientific Reports

Alipour, Hadi H; Abdi, Hossein H; Rahimi, Yousef Y; Bihamta, Mohammad Reza MR

Publication Date: 2021-09-07

Variant appearance in text: rs6859

PubMed Link: 34493739

Variant Present in the following documents:

• Main text
• 41598_2021_Article_96576.pdf

View BVdb publication page

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Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer

Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC

Publication Date: 2021-05-29

Variant appearance in text: NECTIN2: 1043-3434A>G; rs6859

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

View BVdb publication page

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Association Analysis of Polymorphisms in BIN1, MC1R, STARD6 and PVRL2 with Mild Cognitive Impairment in Elderly Carrying APOE ε4 Allele.

Neuropsychiatric Disease And Treatment

Wu, Yue Y; Yin, Jiajun J; Yang, Bixiu B; Tang, Li L; Feng, Wei W; Liu, Xiaowei X; Zhao, Xingfu X; Cheng, Zaohuo Z

Publication Date: 2021

Variant appearance in text: rs6859

PubMed Link: 33907405

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Variability in Molecular Pathways Implicated in Alzheimer's Disease: A Comprehensive Review.

Frontiers In Aging Neuroscience

Vogrinc, David D; Goričar, Katja K; Dolžan, Vita V

Publication Date: 2021

Variant appearance in text: rs6859

PubMed Link: 33815092

Variant Present in the following documents:

• Main text
• fnagi-13-646901.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: rs6859

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Haplotype architecture of the Alzheimer's risk in the APOE region via co-skewness.

Alzheimer'S & Dementia (Amsterdam, Netherlands)

Kulminski, Alexander M AM; Philipp, Ian I; Loika, Yury Y; He, Liang L; Culminskaya, Irina I

Publication Date: 2020

Variant appearance in text: rs6859

PubMed Link: 33204816

Variant Present in the following documents:

• Main text

View BVdb publication page

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Prediction of Alzheimer's disease using multi-variants from a Chinese genome-wide association study.

Brain : A Journal Of Neurology

Jia, Longfei L; Li, Fangyu F; Wei, Cuibai C; Zhu, Min M; Qu, Qiumin Q; Qin, Wei W; Tang, Yi Y; Shen, Luxi L; Wang, Yanjiang Y; Shen, Lu L; Li, Honglei H; Peng, Dantao D; Tan, Lan L; Luo, Benyan B; Guo, Qihao Q; Tang, Muni M; Du, Yifeng Y; Zhang, Jiewen J; Zhang, Junjian J; Lyu, Jihui J; Li, Ying Y; Zhou, Aihong A; Wang, Fen F; Chu, Changbiao C; Song, Haiqing H; Wu, Liyong L; Zuo, Xiumei X; Han, Yue Y; Liang, Junhua J; Wang, Qi Q; Jin, Hongmei H; Wang, Wei W; Lü, Yang Y; Li, Fang F; Zhou, Yuying Y; Zhang, Wei W; Liao, Zhengluan Z; Qiu, Qiongqiong Q; Li, Yan Y; Kong, Chaojun C; Li, Yan Y; Jiao, Haishan H; Lu, Jie J; Jia, Jianping J

Publication Date: 2021-04-12

Variant appearance in text: rs6859

PubMed Link: 33188687

Variant Present in the following documents:

• Main text

View BVdb publication page

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Role of m6A RNA methylation in cardiovascular disease (Review).

International Journal Of Molecular Medicine

Qin, Yuhan Y; Li, Linqing L; Luo, Erfei E; Hou, Jiantong J; Yan, Gaoliang G; Wang, Dong D; Qiao, Yong Y; Tang, Chengchun C

Publication Date: 2020-12

Variant appearance in text: rs6859

PubMed Link: 33125109

Variant Present in the following documents:

• Main text
• ijmm-46-06-1958.pdf

View BVdb publication page

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Characterizing Clinical and Neuropathological Traits of APOE Haplotypes in African Americans and Europeans.

Journal Of Alzheimer'S Disease : Jad

Mezlini, Aziz M AM; Magdamo, Colin C; Merrill, Emily E; Chibnik, Lori B LB; Blacker, Deborah L DL; Hyman, Bradley T BT; Das, Sudeshna S

Publication Date: 2020

Variant appearance in text: rs6859

PubMed Link: 33016904

Variant Present in the following documents:

• Main text

View BVdb publication page

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Plasma lipid levels and risk of primary open angle glaucoma: a genetic study using Mendelian randomization.

Bmc Ophthalmology

Xu, Mengqiao M; Li, Shengguo S; Zhu, Jundong J; Luo, Dawei D; Song, Weitao W; Zhou, Minwen M

Publication Date: 2020-10-02

Variant appearance in text: rs6859

PubMed Link: 33008364

Variant Present in the following documents:

• Main text
• 12886_2020_Article_1661.pdf

View BVdb publication page

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m6A RNA Methylation in Cardiovascular Diseases.

Molecular Therapy : The Journal Of The American Society Of Gene Therapy

Wu, Siyi S; Zhang, Shuchen S; Wu, Xiaoguang X; Zhou, Xiang X

Publication Date: 2020-10-07

Variant appearance in text: rs6859

PubMed Link: 32910911

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic and polygenic risk score analysis for Alzheimer's disease in the Chinese population.

Alzheimer'S & Dementia (Amsterdam, Netherlands)

Zhou, Xiaopu X; Chen, Yu Y; Ip, Fanny C F FCF; Lai, Nicole C H NCH; Li, Yolanda Y T YYT; Jiang, Yuanbing Y; Zhong, Huan H; Chen, Yuewen Y; Zhang, Yulin Y; Ma, Shuangshuang S; Lo, Ronnie M N RMN; Cheung, Kit K; Tong, Estella P S EPS; Ko, Ho H; Shoai, Maryam M; Mok, Kin Y KY; Hardy, John J; Mok, Vincent C T VCT; Kwok, Timothy C Y TCY; Fu, Amy K Y AKY; Ip, Nancy Y NY

Publication Date: 2020

Variant appearance in text: rs6859

PubMed Link: 32775599

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrative Genomic Analysis Predicts Regulatory Role of N 6-Methyladenosine-Associated SNPs for Adiposity.

Frontiers In Cell And Developmental Biology

Lin, Weimin W; Xu, Hao H; Yuan, Quan Q; Zhang, Shiwen S

Publication Date: 2020

Variant appearance in text: rs6859

PubMed Link: 32733881

Variant Present in the following documents:

• Main text
• fcell-08-00551.pdf

View BVdb publication page

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Association of the NCAN-TM6SF2-CILP2-PBX4-SUGP1-MAU2 SNPs and gene-gene and gene-environment interactions with serum lipid levels.

Aging

Deng, Guo-Xiong GX; Yin, Rui-Xing RX; Guan, Yao-Zong YZ; Liu, Chun-Xiao CX; Zheng, Peng-Fei PF; Wei, Bi-Liu BL; Wu, Jin-Zhen JZ; Miao, Liu L

Publication Date: 2020-06-22

Variant appearance in text: rs6859

PubMed Link: 32568739

Variant Present in the following documents:

• Main text
• aging-12-103361.pdf

View BVdb publication page

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Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis

Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q

Publication Date: 2020-09

Variant appearance in text: rs6859

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Shared (epi)genomic background connecting neurodegenerative diseases and type 2 diabetes.

World Journal Of Diabetes

Caputo, Valerio V; Termine, Andrea A; Strafella, Claudia C; Giardina, Emiliano E; Cascella, Raffaella R

Publication Date: 2020-05-15

Variant appearance in text: rs6859

PubMed Link: 32477452

Variant Present in the following documents:

• Main text
• WJD-11-155.pdf

View BVdb publication page

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MAPT haplotype-stratified GWAS reveals differential association for AD risk variants.

Alzheimer'S & Dementia : The Journal Of The Alzheimer'S Association

Strickland, Samantha L SL; Reddy, Joseph S JS; Allen, Mariet M; N'songo, Aurelie A; Burgess, Jeremy D JD; Corda, Morgane M MM; Ballard, Travis T; Wang, Xue X; Carrasquillo, Minerva M MM; Biernacka, Joanna M JM; Jenkins, Gregory D GD; Mukherjee, Shubhabrata S; Boehme, Kevin K; Crane, Paul P; Kauwe, John S JS; Ertekin-Taner, Nilüfer N; ,

Publication Date: 2020-07

Variant appearance in text: rs6859

PubMed Link: 32400971

Variant Present in the following documents:

• Main text

View BVdb publication page

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A polygenic biomarker to identify patients with severe hypercholesterolemia of polygenic origin.

Molecular Genetics & Genomic Medicine

Leal, Luis G LG; Hoggart, Clive C; Jarvelin, Marjo-Riitta MR; Herzig, Karl-Heinz KH; Sternberg, Michael J E MJE; David, Alessia A

Publication Date: 2020-06

Variant appearance in text: rs6859

PubMed Link: 32307928

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic and regulatory architecture of Alzheimer's disease in the APOE region.

Alzheimer'S & Dementia (Amsterdam, Netherlands)

Kulminski, Alexander M AM; Shu, Leonardo L; Loika, Yury Y; He, Liang L; Nazarian, Alireza A; Arbeev, Konstantin K; Ukraintseva, Svetlana S; Yashin, Anatoliy A; Culminskaya, Irina I

Publication Date: 2020

Variant appearance in text: rs6859

PubMed Link: 32211503

Variant Present in the following documents:

• Main text
• DAD2-12-e12008.pdf
• DAD2-12-e12008-s007.xlsx, sheet 1

View BVdb publication page

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DNA methylation QTL analysis identifies new regulators of human longevity.

Human Molecular Genetics

Szymczak, Silke S; Dose, Janina J; Torres, Guillermo G GG; Heinsen, Femke-Anouska FA; Venkatesh, Geetha G; Datlinger, Paul P; Nygaard, Marianne M; Mengel-From, Jonas J; Flachsbart, Friederike F; Klapper, Wolfram W; Christensen, Kaare K; Lieb, Wolfgang W; Schreiber, Stefan S; Häsler, Robert R; Bock, Christoph C; Franke, Andre A; Nebel, Almut A

Publication Date: 2020-05-08

Variant appearance in text: rs6859

PubMed Link: 32160291

Variant Present in the following documents:

• Main text
• ddaa033.pdf

View BVdb publication page

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Selecting likely causal risk factors from high-throughput experiments using multivariable Mendelian randomization.

Nature Communications

Zuber, Verena V; Colijn, Johanna Maria JM; Klaver, Caroline C; Burgess, Stephen S

Publication Date: 2020-01-07

Variant appearance in text: rs6859

PubMed Link: 31911605

Variant Present in the following documents:

• Main text

View BVdb publication page

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PheGWAS: a new dimension to visualize GWAS across multiple phenotypes.

Bioinformatics (Oxford, England)

George, Gittu G; Gan, Sushrima S; Huang, Yu Y; Appleby, Philip P; Nar, A S AS; Venkatesan, Radha R; Mohan, Viswanathan V; Palmer, Colin N A CNA; Doney, Alex S F ASF

Publication Date: 2020-04-15

Variant appearance in text: rs6859

PubMed Link: 31860083

Variant Present in the following documents:

• Main text
• btz944.pdf

View BVdb publication page

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Robust methods in Mendelian randomization via penalization of heterogeneous causal estimates.

Plos One

Rees, Jessica M B JMB; Wood, Angela M AM; Dudbridge, Frank F; Burgess, Stephen S

Publication Date: 2019

Variant appearance in text: rs6859

PubMed Link: 31545794

Variant Present in the following documents:

• Main text

View BVdb publication page

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The role of CD2AP in the Pathogenesis of Alzheimer's Disease.

Aging And Disease

Tao, Qing-Qing QQ; Chen, Yu-Chao YC; Wu, Zhi-Ying ZY

Publication Date: 2019-08

Variant appearance in text: rs6859

PubMed Link: 31440393

Variant Present in the following documents:

• Main text
• ad-10-4-901.pdf

View BVdb publication page

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Evaluation of the Common Molecular Basis in Alzheimer's and Parkinson's Diseases.

International Journal Of Molecular Sciences

Rana, Pratip P; Franco, Edian F EF; Rao, Yug Y; Syed, Khajamoinuddin K; Barh, Debmalya D; Azevedo, Vasco V; Ramos, Rommel T J RTJ; Ghosh, Preetam P

Publication Date: 2019-07-30

Variant appearance in text: rs6859

PubMed Link: 31366155

Variant Present in the following documents:

• Main text

View BVdb publication page

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Polygenic Risk Score for Alzheimer's Disease Is Associated With Ch4 Volume in Normal Subjects.

Frontiers In Genetics

Wang, Tao T; Han, Zhifa Z; Yang, Yu Y; Tian, Rui R; Zhou, Wenyang W; Ren, Peng P; Wang, Pingping P; Zong, Jian J; Hu, Yang Y; Jiang, Qinghua Q

Publication Date: 2019

Variant appearance in text: rs6859

PubMed Link: 31354783

Variant Present in the following documents:

• Main text

View BVdb publication page

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Non-coding variability at the APOE locus contributes to the Alzheimer's risk.

Nature Communications

Zhou, Xiaopu X; Chen, Yu Y; Mok, Kin Y KY; Kwok, Timothy C Y TCY; Mok, Vincent C T VCT; Guo, Qihao Q; Ip, Fanny C FC; Chen, Yuewen Y; Mullapudi, Nandita N; , ; Giusti-Rodríguez, Paola P; Sullivan, Patrick F PF; Hardy, John J; Fu, Amy K Y AKY; Li, Yun Y; Ip, Nancy Y NY

Publication Date: 2019-07-25

Variant appearance in text: rs6859

PubMed Link: 31346172

Variant Present in the following documents:

• Main text
• 41467_2019_Article_10945.pdf
• 41467_2019_10945_MOESM1_ESM.pdf

View BVdb publication page

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Identification of Alzheimer's Disease-Related Genes Based on Data Integration Method.

Frontiers In Genetics

Hu, Yang Y; Zhao, Tianyi T; Zang, Tianyi T; Zhang, Ying Y; Cheng, Liang L

Publication Date: 2018

Variant appearance in text: rs6859

PubMed Link: 30740125

Variant Present in the following documents:

• Main text
• fgene-09-00703.pdf

View BVdb publication page

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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: NECTIN2: 1043-3434A>G; rs6859

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

View BVdb publication page

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Using Multi-Scale Genetic, Neuroimaging and Clinical Data for Predicting Alzheimer's Disease and Reconstruction of Relevant Biological Mechanisms.

Scientific Reports

Khanna, Shashank S; Domingo-Fernández, Daniel D; Iyappan, Anandhi A; Emon, Mohammad Asif MA; Hofmann-Apitius, Martin M; Fröhlich, Holger H

Publication Date: 2018-07-24

Variant appearance in text: rs6859

PubMed Link: 30042519

Variant Present in the following documents:

• Main text
• 41598_2018_Article_29433.pdf

View BVdb publication page

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Apolipoprotein E region molecular signatures of Alzheimer's disease.

Aging Cell

Kulminski, Alexander M AM; Huang, Jian J; Wang, Jiayi J; He, Liang L; Loika, Yury Y; Culminskaya, Irina I

Publication Date: 2018-08

Variant appearance in text: rs6859

PubMed Link: 29797398

Variant Present in the following documents:

• Main text
• ACEL-17-na.pdf

View BVdb publication page

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BCL3-PVRL2-TOMM40 SNPs, gene-gene and gene-environment interactions on dyslipidemia.

Scientific Reports

Miao, Liu L; Yin, Rui-Xing RX; Pan, Shang-Ling SL; Yang, Shuo S; Yang, De-Zhai DZ; Lin, Wei-Xiong WX

Publication Date: 2018-04-18

Variant appearance in text: rs6859

PubMed Link: 29670124

Variant Present in the following documents:

• Main text

View BVdb publication page

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