Ecosyste.ms: Papers
An open API service providing mapping between scientific papers and software projects that are mentioned in them.
All mentions data is based on the CZI Software Mentions dataset.
Projects: cran: SMR
https://packages.ecosyste.ms/registries/cran.r-project.org/packages/SMR
Externally Studentized Midrange Distribution
5 versions
Latest release: about 1 year ago
3 dependent packages
427 downloads last month
Papers Mentioning SMR 65
10.1371/journal.pgen.1008927
On the cross-population generalizability of gene expression prediction modelsCited by: 34
Author(s): Kevin L. Keys, Angel C. Y. Mak, Marquitta J. White, Walter L. Eckalbar, Andrew Dahl, Joel Mefford, Anna V. Mikhaylova, María G. Contreras, Jennifer R. Elhawary, Celeste Eng, Donglei Hu, Scott Huntsman, Sam S. Oh, Sandra Salazar, Michael A. LeNoir, Jimmie C. Ye, Timothy A. Thornton, Noah Zaitlen, Esteban G. Burchard, Christopher R. Gignoux
Software Mentions: 16
Published: over 4 years ago
10.1371/journal.pgen.1009331
A 12 kb multi-allelic copy number variation encompassing a GC gene enhancer is associated with mastitis resistance in dairy cattleCited by: 20
Author(s): Young Lim Lee, Hitoshi Takeda, Gabriel Costa Monteiro Moreira, Latifa Karim, Erik Mullaart, Wouter Coppieters, Ruth Appeltant, R.F. Veerkamp, Martien A. M. Groenen, Michel Georges, Mirte Bosse, Tom Druet, A.C. Bouwman, Carole Charlier
Software Mentions: 7
Published: over 3 years ago
10.1038/s41597-020-00659-z
lncRNAKB, a knowledgebase of tissue-specific functional annotation and trait association of long noncoding RNACited by: 35
Author(s): Fayaz Seifuddin, Komudi Singh, Abhilash Suresh, Jennifer Judy, Yun Ching Chen, Vijender Chaitankar, Ilker Tunc, Xiangbo Ruan, Ping Li, Yi Chen, Haiming Cao, Richard S. Lee, Fernando S. Goes, Peter P. Zandi, M. Saleet Jafri, Mehdi Pirooznia
Software Mentions: 7
Published: about 4 years ago
10.7554/eLife.34408
The MR-Base platform supports systematic causal inference across the human phenomeCited by: 2,864
Author(s): Gibran Hemani, Jie Zheng, Benjamin Elsworth, Kaitlin H Wade, Valeriia Haberland, Denis Baird, Charles Laurin, Stephen Burgess, Jack Bowden, Ryan Langdon, Vanessa Tan, James Yarmolinsky, Hashem A. Shihab, Nicholas J. Timpson, David M. Evans, Caroline L Relton, Richard M. Martin, George Davey Smith, Tom R. Gaunt, Philip Haycock
Software Mentions: 6
Published: over 6 years ago
10.1002/mds.28197
The Parkinson's Disease <scp>Genome‐Wide</scp> Association Study Locus BrowserCited by: 61
Author(s): Francis P. Grenn, Jonggeol J. Kim, Mary B. Makarious, Hirotaka Iwaki, Anastasia Illarionova, Kajsa Brolin, Jillian H. Kluss, Artur Schumacher-Schuh, Hampton Leonard, Faraz Faghri, Kimberley Billingsley, Lynne Krohn, Ashley Hall, Mónica Díez-Fairén, María Teresa Periñán, Jia Nee Foo, Cynthia Sandor, Caleb Webber, Brian Fiske, J. Raphael Gibbs, Mike A. Nalls, Andrew B. Singleton, Sara Bandrés‐Ciga, Xylena Reed, Cornelis Blauwendraat
Software Mentions: 5
Published: about 4 years ago
10.1371/journal.pgen.1009455
MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneityCited by: 19
Author(s): Anqi Zhu, Nana Matoba, Emmaleigh Wilson, Amanda L. Tapia, Yun Li, Joseph G. Ibrahim, Jason L. Stein, Michael I. Love
Software Mentions: 5
Published: over 3 years ago
10.1038/s42003-021-01784-0
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconusCited by: 36
Author(s): Alison J. Hardcastle, Petra Lišková, Yelena Bykhovskaya, Bennet J McComish, Alice E. Davidson, Chris F. Inglehearn, Xiaohui Li, Hélène Choquet, Mahmoud Habeeb, Sionne E. M. Lucas, Srujana Sahebjada, Nikolas Pontikos, Karla E. Rojas López, Anthony P Khawaja, Manir Ali, Ľubica Ďuďáková, Pavlína Skalická, Bart T. H. van Dooren, Annette J M Geerards, Christoph Haudum, Valeria Lo Faro, Abi Tenen, Mark James Simcoe, Karina Patasova, Darioush Yarrand, Jie Yin, Salina Siddiqui, Anthony J. Rice, Layal Abi Farraj, Yii Der Ida Chen, Jugnoo S Rahi, Ronald M. Krauss, Elizabeth Theusch, Jac Charlesworth, Loretta Szczotka-Flynn, Carmel Toomes, Magda A. Meester-Smoor, Andrea J. Richardson, Paul Mitchell, Kent D. Taylor, Ronald B. Melles, Anthony J. Aldave, Richard A. Mills, Ke Cao, Elsie Chan, Mark Daniell, Jie Jin Wang, Jerome I. Rotter, Alex W. Hewitt, Stuart MacGregor, Caroline C W Klaver, Wishal D. Ramdas, Jamie E Craig, Sudha K. Iyengar, David O’Brart, Eric Jorgenson, Paul N. Baird, Yaron S. Rabinowitz, Kathryn P. Burdon, Chris Hammond, Stephen Tuft, Pirro G. Hysi
Software Mentions: 4
Published: over 3 years ago
10.1186/s13059-020-01997-2
Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclastsCited by: 29
Author(s): Benjamin H. Mullin, Jennifer Tickner, Kun Zhu, Jacob Kenny, Shelby Mullin, Suzanne J. Brown, Frank Dudbridge, Nathan J. Pavlos, Edward S. Mocarski, John P. Walsh, Jiake Xu, Scott G. Wilson
Software Mentions: 4
Published: over 4 years ago
10.1186/s13059-020-02248-0
The variant call format provides efficient and robust storage of GWAS summary statisticsCited by: 55
Author(s): M. Lyon, Shea J. Andrews, Benjamin Elsworth, Tom R. Gaunt, Gibran Hemani, Edoardo Marcora
Software Mentions: 4
Published: almost 4 years ago
10.1038/s41398-020-0777-y
Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics dataCited by: 23
Author(s): Huijuan Li, Na Qu, Hui Li, Xin Cai, Chuyi Zhang, Bao‐Liang Zhong, Shufang Zhang, Jing Chen, Bin Xia, Lu Wang, Qi Jia, Wei Li, Hong Chang, Xiao Xiao, Ming Li, Yi Li
Software Mentions: 3
Published: over 4 years ago
10.1016/j.ajhg.2018.09.007
Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex TraitsCited by: 118
Author(s): Eilís Hannon, T.J. Gorrie-Stone, Melissa Smart, Joe Burrage, Amanda Hughes, Yanchun Bao, Meena Kumari, Leonard C Schalkwyk, Jonathan Mill
Software Mentions: 3
Published: about 6 years ago
10.1172/jci.insight.136477
Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPsCited by: 10
Author(s): Xiaofeng Chen, Mingrui Guo, Yuanyuan Duan, Feng Jiang, Hao Wu, Shanshan Dong, Xiaorong Zhou, Hlaing Nwe Thynn, C.C. Liu, Lin Zhang, Yan Guo, Tie‐Lin Yang
Software Mentions: 3
Published: about 4 years ago
10.1371/journal.pone.0176769
Robust auto-weighted multi-view subspace clustering with common subspace representation matrixCited by: 16
Author(s): Wenzhang Zhuge, Chenping Hou, Yuling Jiao, Jia Yue, Tao Hong, Dongyun Yi
Software Mentions: 3
Published: over 7 years ago
10.3389/fgene.2020.00486
Expression Quantitative Trait Loci (eQTL) Mapping in Korean Patients With Crohn’s Disease and Identification of Potential Causal Genes Through Integration With Disease AssociationsCited by: 14
Author(s): Seulgi Jung, Wenting Liu, Jiwon Baek, Jung Won Moon, Byong Duk Ye, Ho‐Su Lee, Sang Hyoung Park, Suk Kyun Yang, Buhm Han, Jing Liu, Kyuyoung Song
Software Mentions: 3
Published: over 4 years ago
10.18632/aging.102230
Epigenome-wide association study of leukocyte telomere lengthCited by: 16
Author(s): Yunsung Lee, Dianjianyi Sun, Anil P.S. Ori, Ake T. Lu, Anne Seeboth, Sarah E. Harris, Ian J. Deary, Riccardo E. Marioni, Mette Soerensen, Jonas Mengel‐From, Jacob Hjelmborg, Kaare Christensen, James G. Wilson, Daniel Levy, Alex P. Reiner, Wei Chen, Shengxu Li, Jennifer R. Harris, Per Magnus, Abraham Aviv, Astanand Jugessur, Steve Horvath
Software Mentions: 2
Published: about 5 years ago
10.1186/s13059-020-02026-y
PTWAS: investigating tissue-relevant causal molecular mechanisms of complex traits using probabilistic TWAS analysisCited by: 41
Author(s): Yuhua Zhang, Corbin Quick, Ketian Yu, Alvaro N. Barbeira, Francesca Luca, Roger Piqué-Regi, Hae Kyung Im, Xiaoquan Wen
Software Mentions: 2
Published: about 4 years ago
10.1186/s13073-019-0613-2
Prioritizing putative influential genes in cardiovascular disease susceptibility by applying tissue-specific Mendelian randomizationCited by: 26
Author(s): Kenneth B. Taylor, George Davey Smith, Caroline L Relton, Tom R. Gaunt, Tom G Richardson
Software Mentions: 2
Published: almost 6 years ago
10.1186/s13073-021-00890-2
Multi-tissue neocortical transcriptome-wide association study implicates 8 genes across 6 genomic loci in Alzheimer’s diseaseCited by: 18
Author(s): Jake Gockley, Kelsey S. Montgomery, William L. Poehlman, Jesse C. Wiley, Yue Liu, Ekaterina S. Gerasimov, Anna K. Greenwood, Solveig K. Sieberts, Thomas S. Wingo, Lara M. Mangravite, Benjamin A. Logsdon
Software Mentions: 2
Published: over 3 years ago
10.1186/s13040-020-00216-9
Identification of therapeutic targets from genetic association studies using hierarchical component analysisCited by: 3
Author(s): Hao-Chih Lee, Osamu Ichikawa, Benjamin S. Glicksberg, Aparna A. Divaraniya, Christine Becker, Pankaj Agarwal, Joel T. Dudley
Software Mentions: 2
Published: over 4 years ago
10.1038/srep41036
Estimating carnivore community structuresCited by: 38
Author(s): José Jímenez, Juan Carlos Nuñez-Arjona, Carmen Rueda, Luis Mariano González, Francisco García‐Dominguez, Jaime Múñoz-Igualada, José Vicente López‐Bao
Software Mentions: 2
Published: almost 8 years ago
10.1371/journal.pone.0188877
Response of pumas (Puma concolor) to migration of their primary prey in PatagoniaCited by: 21
Author(s): Maria L. Gelin, Lyn C. Branch, Daniel H. Thornton, Andrés J. Novaro, Matthew J. Gould, Anthony Caragiulo
Software Mentions: 2
Published: almost 7 years ago
10.1038/s41598-018-29462-y
Genetic regulation of disease risk and endometrial gene expression highlights potential target genes for endometriosis and polycystic ovarian syndromeCited by: 42
Author(s): Jenny N. Fung, Sally Mortlock, Jane E. Girling, Sarah J. Holdsworth-Carson, Wan Tinn Teh, Zhihong Zhu, Samuel W. Lukowski, Brett McKinnon, Allan F. McRae, Jian Yang, Martin Healey, Joseph E. Powell, Peter A. W. Rogers, Grant W. Montgomery
Software Mentions: 2
Published: over 6 years ago
10.3389/fgene.2021.716236
Integrative Transcriptome-Wide Analyses Uncover Novel Risk-Associated MicroRNAs in Hormone-Dependent CancersCited by: 3
Author(s): Dulari K. Jayarathna, Miguel E. Rentería, Adil Malik, Emilie Sauret, Jyotsna Batra, Neha S. Gandhi
Software Mentions: 2
Published: about 3 years ago
10.3390/s140305004
Seluge++: A Secure Over-the-Air Programming Scheme in Wireless Sensor NetworksCited by: 8
Author(s): Farzan Doroodgar, Mohammad A. Razzaque, Ismail Fauzi Isnin
Software Mentions: 2
Published: over 10 years ago
10.1371/journal.pgen.1009405
Power analysis of transcriptome-wide association study: Implications for practical protocol choiceCited by: 37
Author(s): Chen Cao, Bowei Ding, Qing Li, Devin Kwok, Jingjing Wu, Quan Long
Software Mentions: 2
Published: over 3 years ago
10.1186/s13148-019-0648-7
Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseasesCited by: 24
Author(s): Sally Mortlock, Restuadi Restuadi, Rupert Levien, Jane E. Girling, Sarah J. Holdsworth-Carson, Martin Healey, Zhihong Zhu, Ting Qi, Yang Wu, Samuel W. Lukowski, Peter A. W. Rogers, Jian Yang, Allan F. McRae, Jenny N. Fung, Grant W. Montgomery
Software Mentions: 2
Published: over 5 years ago
10.1038/s42003-020-01334-0
The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank studyCited by: 62
Author(s): Yu‐Fang Pei, Yaozhong Liu, Xiaolin Yang, Lei Zhang, Guoliang Feng, Xin‐Tong Wei
Software Mentions: 2
Published: about 4 years ago
10.3389/fpsyt.2020.00256
Integrated Analysis of Summary Statistics to Identify Pleiotropic Genes and Pathways for the Comorbidity of Schizophrenia and Cardiometabolic DiseaseCited by: 22
Author(s): Hao Líu, Yang Sun, Xinxin Zhang, Shiyang Li, Dong Hu, Lei Xiao, Yanghui Chen, Lin He, Dao Wen Wang
Software Mentions: 2
Published: over 4 years ago
10.1038/s41598-018-25065-9
Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAsCited by: 11
Author(s): Tetsuya Hirata, Kaori Koga, Todd A. Johnson, Ryoko Morino, Kazuyuki Nakazono, Shigeo Kamitsuji, Masanori Akita, Maiko Kawajiri, Azusa Kami, Yuria Hoshi, Asami Tada, Ken-ichi Ishikawa, Maaya Hine, Miki Kobayashi, Nami Kurume, Tomoyuki Fujii, Naoyuki Kamatani, Yutaka Osuga
Software Mentions: 1
Published: over 6 years ago
10.1038/s41598-018-27145-2
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associationsCited by: 50
Author(s): Chihiro Endo, Todd A. Johnson, Ryoko Morino, Kazuyuki Nakazono, Shigeo Kamitsuji, Masanori Akita, Maiko Kawajiri, Tatsuya Yamasaki, Azusa Kami, Yuria Hoshi, Asami Tada, Ken-ichi Ishikawa, Maaya Hine, Miki Kobayashi, Nami Kurume, Yuichiro Tsunemi, Naoyuki Kamatani, Makoto Kawashima
Software Mentions: 1
Published: over 6 years ago
10.1038/s41598-021-87219-6
Effect of selection bias on two sample summary data based Mendelian randomizationCited by: 10
Author(s): Kai Wang, Shizhong Han
Software Mentions: 1
Published: over 3 years ago
10.3390/s101009529
A Feedback-Based Secure Path Approach for Wireless Sensor Network Data CollectionCited by: 5
Author(s): Yuxin Mao, Guiyi Wei
Software Mentions: 1
Published: about 14 years ago
10.1038/s41398-018-0114-x
The integrated landscape of causal genes and pathways in schizophreniaCited by: 58
Author(s): Chenhui Ma, Chunjie Gu, Yongxia Huo, Xiaoyan Li, Xiong‐Jian Luo
Software Mentions: 1
Published: over 6 years ago
10.1038/s41398-021-01348-0
Mendelian randomization integrating GWAS and eQTL data revealed genes pleiotropically associated with major depressive disorderCited by: 18
Author(s): Huiru Yang, Di Liu, Chuntao Zhao, Bowen Feng, Wenjin Lu, Xiaohan Yang, Minglu Xu, Weizhu Zhou, Huiquan Jing, Jingyun Yang
Software Mentions: 1
Published: over 3 years ago
10.1186/s40246-021-00307-6
Convergent lines of evidence support BIN1 as a risk gene of Alzheimer’s diseaseCited by: 5
Author(s): Jin Liang Zhu, Xia Liu, Hongtao Yin, Yan Gao, Hao Yu
Software Mentions: 1
Published: almost 4 years ago
10.3390/jimaging7070103
Restoration and Enhancement of Historical Stereo PhotosCited by: 1
Author(s): Marco Fanfani, Colombo Carlo, Fabio Bellavia
Software Mentions: 1
Published: over 3 years ago
10.3390/ijms21197332
Genetic Risk Profiling in Parkinson’s Disease and Utilizing Genetics to Gain Insight into Disease-Related Biological PathwaysCited by: 15
Author(s): Ashley Hall, Sara Bandrés‐Ciga, Mónica Díez-Fairén, John P. Quinn, Kimberley Billingsley
Software Mentions: 1
Published: about 4 years ago
10.3390/nu13061984
Epigenome-Wide Study Identified Methylation Sites Associated with the Risk of ObesityCited by: 6
Author(s): Majid Nikpay, Sepehr Ravati, Robert Dent, Ruth McPherson
Software Mentions: 1
Published: over 3 years ago
10.1186/s13195-018-0458-8
Genome-wide analysis of genetic predisposition to Alzheimer’s disease and related sex disparitiesCited by: 55
Author(s): Alireza Nazarian, Anatoliy I. Yashin, Alexander M. Kulminski
Software Mentions: 1
Published: almost 6 years ago
10.1186/s12864-021-07860-3
Mendelian randomization analysis identified genes pleiotropically associated with central corneal thicknessCited by: 7
Author(s): Zhikun Yang, Jingyun Yang, Di Liu, Weihong Yu
Software Mentions: 1
Published: over 3 years ago
10.1186/s12881-020-0977-6
Disentangling the genetics of sarcopenia: prioritization of NUDT3 and KLF5 as genes for lean mass & HLA-DQB1-AS1 for hand grip strength with the associated enhancing SNPs & a scoring systemCited by: 18
Author(s): Abhishek Narain Singh, Bili Gasman
Software Mentions: 1
Published: over 4 years ago
10.1155/2018/3848560
A Genomewide Integrative Analysis of GWAS and eQTLs Data Identifies Multiple Genes and Gene Sets Associated with ObesityCited by: 7
Author(s): Li Liu, Qunping Fan, Feng Zhang, Xiong Guo, Xiao Liang, Yanan Du, Ping Li, Yan Wen, Jingcan Hao, Wenyu Wang, Awen He
Software Mentions: 1
Published: almost 7 years ago
10.1155/2017/1758636
Integrating Genome-Wide Association and eQTLs Studies Identifies the Genes and Gene Sets Associated with DiabetesCited by: 2
Author(s): Xiao Liang, Awen He, Wenyu Wang, Li Liu, Yanan Du, Qunping Fan, Ping Li, Yan Wen, Jingcan Hao, Xiong Guo, Feng Zhang
Software Mentions: 1
Published: almost 8 years ago
10.1371/journal.pgen.1007799
Genetic regulation of the placental transcriptome underlies birth weight and risk of childhood obesityCited by: 31
Author(s): Shouneng Peng, Maya A. Deyssenroth, Antonio Fabio Di Narzo, Haoxiang Cheng, Zhongyang Zhang, Luca Lambertini, Arno Ruusalepp, Jason C. Kovacic, Johan Björkegren, Carmen J. Marsit, Jia Chen, Ke Hao
Software Mentions: 1
Published: almost 6 years ago
10.1371/journal.pgen.1008785
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traitsCited by: 26
Author(s): Andrew D. Bretherick, Oriol Canela-Xandri, Peter K. Joshi, David W. Clark, Konrad Rawlik, Thibaud Boutin, Yanni Zeng, Carmen Amador, Pau Navarro, Igor Rudan, Alan F. Wright, Harry Campbell, Véronique Vitart, Caroline Hayward, James F. Wilson, Albert Tenesa, Chris P. Ponting, J Kenneth Baillie, Chris Haley
Software Mentions: 1
Published: over 4 years ago
10.1371/journal.pone.0181470
Severe maternal morbidity in Zanzibar’s referral hospital: Measuring the impact of in-hospital careCited by: 25
Author(s): Tanneke Herklots, Lieke van Acht, Tarek Meguid, Arie Franx, Benoit Jacod
Software Mentions: 1
Published: about 7 years ago
10.1371/journal.pone.0213953
Integrating genome-wide association and eQTLs studies identifies the genes associated with age at menarche and age at natural menopauseCited by: 5
Author(s): Gang Wang, Jian Lv, Xiaoxin Qiu, Yujun An
Software Mentions: 1
Published: over 5 years ago
10.1016/j.cell.2016.10.042
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseCited by: 962
Author(s): William Astle, Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice Mann, Daniel Mead, H. J. Bouman, Fernando Riveros-Mckay, Myrto Kostadima, John Lambourne, Suthesh Sivapalaratnam, Kate Downes, Kousik Kundu, Lorenzo Bomba, Kim Berentsen, John R. Bradley, Louise C. Daugherty, Olivier Delaneau, Kathleen Freson, Stephen F. Garner, Luigi Grassi, José Antonio López Guerrero, Matthias Haimel, Eva M. Janssen-Megens, Anita Kaan, Mihir Kamat, Bowon Kim, Amit Mandoli, Jonathan Marchini, Joost H.A. Martens, Stuart Meacham, Karyn Mégy, Jared O’Connell, R. Petersen, Nilofar Sharifi, Simon Sheard, James R Staley, Salih Tuna, Martijn van der Ent, Klaudia Walter, Shuang-Yin Wang, Eleanor Wheeler, Steven P. Wilder, Valentina Iotchkova, Carmel Moore, Jennifer Sambrook, Hendrik G. Stunnenberg, Emanuele Di Angelantonio, Stephen Kaptoge, Taco W. Kuijpers, Enrique Carrillo de Santa Pau, David Juan, Daniel Rico, Alfonso Valencia, Ciyong Lu, Bing Ge, Louella Vasquez, Tony Kwan, Diego Garrido-Martín, Stephen Watt, Ying Yang, Roderic Guigó, Stephan Beck, Dirk S. Paul, Tomi Pastinen, David Bujold, Guillaume Bourque, Mattia Frontini, John Danesh, David J. Roberts, Willem H. Ouwehand, Adam S. Butterworth, Nicole Soranzo
Software Mentions: 1
Published: about 8 years ago
10.1155/2018/4617816
Different Performances of Different Intelligent Algorithms for Solving FJSP: A Perspective of StructureCited by: 5
Author(s): Xiaohu Shi, Wei Long, Yan-Yan Li, Yonglai Wei, Dayong Deng
Software Mentions: 1
Published: about 6 years ago
10.1002/ece3.5077
Generalized spatial mark–resight models with incomplete identification: An application to red fox density estimatesCited by: 27
Author(s): José Jímenez, Richard B. Chandler, Jorge Tobajas, Esther Descalzo, Rafael Mateo, Pablo Ferreras
Software Mentions: 1
Published: over 5 years ago
10.3389/fcell.2020.00472
Identifying Protein Biomarkers in Blood for Alzheimer's DiseaseCited by: 7
Author(s): Tianyi Zhao, Yang Hu, Tianyi Zang, Yadong Wang
Software Mentions: 1
Published: over 4 years ago
10.3389/fgene.2019.00511
A Trans-Ethnic Genome-Wide Association Study of Uterine FibroidsCited by: 27
Author(s): Todd L. Edwards, Ayush Giri, Jacklyn N. Hellwege, Katherine E. Hartmann, Elizabeth A. Stewart, Janina M. Jeff, Michael J. Bray, Sarah A. Pendergrass, Eric S. Torstenson, Jacob M. Keaton, Sara Jones, Radhika Gogoi, Helena Kuivaniemi, Kathryn Jackson, Abel N. Kho, Iftikhar J. Kullo, Catherine A. McCarty, Hae Kyung Im, Jennifer A. Pacheco, Jyotishman Pathak, Marc S. Williams, Gerard Tromp, Eimear E. Kenny, Peggy L. Peissig, Joshua C. Denny, Dan M. Roden, Digna R. Velez Edwards
Software Mentions: 1
Published: over 5 years ago
10.3389/fgene.2020.00424
From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex DiseasesCited by: 271
Author(s): Eddie Cano-Gamez, Gosia Trynka
Software Mentions: 1
Published: over 4 years ago
10.3389/fgene.2021.726599
Genetic Mechanism Revealed of Age-Related Macular Degeneration Based on Fusion of Statistics and Machine Learning MethodCited by: 1
Author(s): Yongyi Du, Ning Kong, Jibin Zhang
Software Mentions: 1
Published: over 3 years ago
10.3389/fgene.2020.00060
Mendelian Randomization Identifies CpG Methylation Sites With Mediation Effects for Genetic Influences on BMD in Peripheral Blood MonocytesCited by: 8
Author(s): Fangtang Yu, Chuan Qiu, Chao Xu, Qing Tian, Lan‐Juan Zhao, Lijun Wu, Hong‐Wen Deng, Hui Shen
Software Mentions: 1
Published: over 4 years ago
10.3389/fgene.2020.00320
The Integrated Landscape of Biological Candidate Causal Genes in Coronary Artery DiseaseCited by: 11
Author(s): Qiwen Zheng, Yujia Ma, Si Chen, Qianzi Che, Dafang Chen
Software Mentions: 1
Published: over 4 years ago
10.3389/fgene.2019.01336
Integrating Multi-Omics Data to Identify Novel Disease Genes and Single-Neucleotide PolymorphismsCited by: 7
Author(s): Song Zhao, Huijie Jiang, Zonghui Liang, Hong Ju
Software Mentions: 1
Published: almost 5 years ago
10.3389/fgene.2021.728563
Identification of New Genes and Loci Associated With Bone Mineral Density Based on Mendelian RandomizationCited by: 3
Author(s): Yijun Liu, Guang Jin, Xue Wang, Ying Dong, Fupeng Ding
Software Mentions: 1
Published: about 3 years ago
10.3389/fnhum.2017.00356
Resting-State Fluctuations of EEG Sensorimotor Rhythm Reflect BOLD Activities in the Pericentral Areas: A Simultaneous EEG-fMRI StudyCited by: 20
Author(s): Shohei Tsuchimoto, Shuka Shibusawa, Nobuaki Mizuguchi, Kenji Kato, Hiroki Ebata, Meigen Liu, Takashi Hanakawa, Junichi Ushiba
Software Mentions: 1
Published: over 7 years ago
10.3389/fneur.2019.00517
Integrative Analysis Identified IRF6 and NDST1 as Potential Causal Genes for Ischemic StrokeCited by: 13
Author(s): Xing‐Bo Mo, Shu‐Feng Lei, Yonghong Zhang, Huan Zhang
Software Mentions: 1
Published: over 5 years ago
10.3389/fnsys.2012.00070
ADHD diagnosis from multiple data sources with batch effectsCited by: 17
Author(s): Emanuele Olivetti, Susanne Greiner, Paolo Avesani
Software Mentions: 1
Published: almost 13 years ago
10.3390/genes11091100
Identifying Risk Genes and Interpreting Pathogenesis for Parkinson’s Disease by a Multiomics AnalysisCited by: 11
Author(s): Wenwen Cheng, Qiang Zhu, Hongyu Zhang
Software Mentions: 1
Published: about 4 years ago
10.1186/s13073-016-0338-4
Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traitsCited by: 84
Author(s): Jennifer M. Whitehead Pavlides, Zhihong Zhu, Jacob Gratten, Allan F. McRae, Naomi R. Wray, Jian Yang
Software Mentions: 1
Published: over 8 years ago
10.3390/jcm9051489
Summary-Based Methylome-Wide Association Analyses Suggest Potential Genetically Driven Epigenetic Heterogeneity of Alzheimer’s DiseaseCited by: 9
Author(s): Alireza Nazarian, Anatoliy I. Yashin, Alexander M. Kulminski
Software Mentions: 1
Published: over 4 years ago
10.1093/schbul/sbab032
Integrative Analyses Followed by Functional Characterization Reveal <i>TMEM180</i> as a Schizophrenia Risk GeneCited by: 7
Author(s): Jun-Yang Wang, Xiaoyan Li, Huijuan Li, Jie-wei Liu, Yong-Gang Yao, Ming Li, Xiao Xiao, Xiong-Jian Luo
Software Mentions: 1
Published: over 3 years ago