These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 24834846)

  • 61. Genetic susceptibility to multiple sclerosis in African Americans.
    Goodin DS; Oksenberg JR; Douillard V; Gourraud PA; Vince N
    PLoS One; 2021; 16(8):e0254945. PubMed ID: 34370753
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Genetic susceptibility to multiple sclerosis: interactions between conserved extended haplotypes of the MHC and other susceptibility regions.
    Goodin DS; Khankhanian P; Gourraud PA; Vince N
    BMC Med Genomics; 2021 Jul; 14(1):183. PubMed ID: 34246256
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Minireview: Novel Micropeptide Discovery by Proteomics and Deep Sequencing Methods.
    Tharakan R; Sawa A
    Front Genet; 2021; 12():651485. PubMed ID: 34025718
    [TBL] [Abstract][Full Text] [Related]  

  • 64. The nature of genetic and environmental susceptibility to multiple sclerosis.
    Goodin DS; Khankhanian P; Gourraud PA; Vince N
    PLoS One; 2021; 16(3):e0246157. PubMed ID: 33750973
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Integrated Network and Gene Ontology Analysis Identifies Key Genes and Pathways for Coronary Artery Diseases.
    Prakash T; Ramachandra NB
    Avicenna J Med Biotechnol; 2021; 13(1):15-23. PubMed ID: 33680369
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment.
    Cerván-Martín M; Bossini-Castillo L; Rivera-Egea R; Garrido N; Luján S; Romeu G; Santos-Ribeiro S; Ivirma Group ; Lisbon Clinical Group ; Castilla JA; Gonzalvo MC; Clavero A; Vicente FJ; Guzmán-Jiménez A; Costa C; Llinares-Burguet I; Khantham C; Burgos M; Barrionuevo FJ; Jiménez R; Sánchez-Curbelo J; López-Rodrigo O; Peraza MF; Pereira-Caetano I; Marques PI; Carvalho F; Barros A; Bassas L; Seixas S; Gonçalves J; Larriba S; Lopes AM; Palomino-Morales RJ; Carmona FD
    J Pers Med; 2020 Dec; 11(1):. PubMed ID: 33383876
    [TBL] [Abstract][Full Text] [Related]  

  • 67. The Biological Significance of Multi-copy Regions and Their Impact on Variant Discovery.
    Sun J; Zhang Y; Wang M; Guan Q; Yang X; Ou JX; Yan M; Wang C; Zhang Y; Li ZH; Lan C; Mao C; Zhou HW; Hao B; Zhang Z
    Genomics Proteomics Bioinformatics; 2020 Oct; 18(5):516-524. PubMed ID: 32827758
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the Clinic.
    Cerván-Martín M; Castilla JA; Palomino-Morales RJ; Carmona FD
    J Clin Med; 2020 Jan; 9(2):. PubMed ID: 31973052
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence.
    Hsieh AR; Chen LS; Li YJ; Fann CSJ
    Psychiatr Genet; 2019 Aug; 29(4):111-119. PubMed ID: 31033776
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.
    Coltell O; Asensio EM; Sorlí JV; Barragán R; Fernández-Carrión R; Portolés O; Ortega-Azorín C; Martínez-LaCruz R; González JI; Zanón-Moreno V; Gimenez-Alba I; Fitó M; Ros E; Ordovas JM; Corella D
    Nutrients; 2019 Jan; 11(1):. PubMed ID: 30621171
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Highly conserved extended haplotypes of the major histocompatibility complex and their relationship to multiple sclerosis susceptibility.
    Goodin DS; Khankhanian P; Gourraud PA; Vince N
    PLoS One; 2018; 13(2):e0190043. PubMed ID: 29438392
    [TBL] [Abstract][Full Text] [Related]  

  • 72. A non-threshold region-specific method for detecting rare variants in complex diseases.
    Hsieh AR; Chen DP; Chattopadhyay AS; Li YJ; Chang CC; Fann CSJ
    PLoS One; 2017; 12(11):e0188566. PubMed ID: 29190701
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Lifestyle Medicine: A Brief Review of Its Dramatic Impact on Health and Survival.
    Bodai BI; Nakata TE; Wong WT; Clark DR; Lawenda S; Tsou C; Liu R; Shiue L; Cooper N; Rehbein M; Ha BP; Mckeirnan A; Misquitta R; Vij P; Klonecke A; Mejia CS; Dionysian E; Hashmi S; Greger M; Stoll S; Campbell TM
    Perm J; 2018; 22():17-025. PubMed ID: 29035175
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target.
    Jo M; Chung AY; Yachie N; Seo M; Jeon H; Nam Y; Seo Y; Kim E; Zhong Q; Vidal M; Park HC; Roth FP; Suk K
    Genome Res; 2017 Sep; 27(9):1487-1500. PubMed ID: 28596290
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Big genomics and clinical data analytics strategies for precision cancer prognosis.
    Ow GS; Kuznetsov VA
    Sci Rep; 2016 Nov; 6():36493. PubMed ID: 27819294
    [TBL] [Abstract][Full Text] [Related]  

  • 76. The nature of genetic susceptibility to multiple sclerosis: constraining the possibilities.
    Goodin DS
    BMC Neurol; 2016 Apr; 16():56. PubMed ID: 27117889
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Systems Genetic Validation of the SNP-Metabolite Association in Rice Via Metabolite-Pathway-Based Phenome-Wide Association Scans.
    Lu Y; Liu Y; Niu X; Yang Q; Hu X; Zhang HY; Xia J
    Front Plant Sci; 2015; 6():1027. PubMed ID: 26640468
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray.
    Coleman JR; Euesden J; Patel H; Folarin AA; Newhouse S; Breen G
    Brief Funct Genomics; 2016 Jul; 15(4):298-304. PubMed ID: 26443613
    [TBL] [Abstract][Full Text] [Related]  

  • 79. The ABCC6 Transporter as a Paradigm for Networking from an Orphan Disease to Complex Disorders.
    De Vilder EY; Hosen MJ; Vanakker OM
    Biomed Res Int; 2015; 2015():648569. PubMed ID: 26356190
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Haplotype-based approach to known MS-associated regions increases the amount of explained risk.
    Khankhanian P; Gourraud PA; Lizee A; Goodin DS
    J Med Genet; 2015 Sep; 52(9):587-94. PubMed ID: 26185143
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.