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                             19 results found
no title author magazine year volume issue page(s) type
1 Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project Machini, Kalotina
2019
105 1 p. 177-188
article
2 Australian Genomics: A Federated Model for Integrating Genomics into Healthcare Stark, Zornitza
2019
105 1 p. 7-14
article
3 Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS Rafehi, Haloom
2019
105 1 p. 151-165
article
4 David “DJ” Weatherall Peto, Tim E.
2019
105 1 p. 3-6
article
5 De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders Dulovic-Mahlow, Marija
2019
105 1 p. 213-220
article
6 Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology Spracklen, Cassandra N.
2019
105 1 p. 15-28
article
7 Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders Tian, Yun
2019
105 1 p. 166-176
article
8 Fast and Accurate Shared Segment Detection and Relatedness Estimation in Un-phased Genetic Data via TRUFFLE Dimitromanolakis, Apostolos
2019
105 1 p. 78-88
article
9 Genes for Good: Engaging the Public in Genetics Research via Social Media Brieger, Katharine
2019
105 1 p. 65-77
article
10 Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human Liver Çalışkan, Minal
2019
105 1 p. 89-107
article
11 Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia Whitfield, Marjorie
2019
105 1 p. 198-212
article
12 NCALD Antisense Oligonucleotide Therapy in Addition to Nusinersen further Ameliorates Spinal Muscular Atrophy in Mice Torres-Benito, Laura
2019
105 1 p. 221-230
article
13 Pathogenic Variants in NUP214 Cause “Plugged” Nuclear Pore Channels and Acute Febrile Encephalopathy Fichtman, Boris
2019
105 1 p. 48-64
article
14 Public Discussion Affects Question Asking at Academic Conferences Telis, Natalie
2019
105 1 p. 189-197
article
15 RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities Cousin, Margot A.
2019
105 1 p. 108-121
article
16 Systematic Functional Interrogation of Genes in GWAS Loci Identified ATF1 as a Key Driver in Colorectal Cancer Modulated by a Promoter-Enhancer Interaction Tian, Jianbo
2019
105 1 p. 29-47
article
17 The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance Pehlivan, Davut
2019
105 1 p. 132-150
article
18 Third-Party Genetic Interpretation Tools: A Mixed-Methods Study of Consumer Motivation and Behavior Nelson, Sarah C.
2019
105 1 p. 122-131
article
19 This Month in The Journal Ratzel, Sarah
2019
105 1 p. 1-2
article
                             19 results found
 
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