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1
Global sites for mutations of unknown origins
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Global sites for mutations of unknown origins

Nature (London), 2024-05, Vol.629 (8013), p.767-768 [Peer Reviewed Journal]

Copyright Nature Publishing Group May 23, 2024 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/d41586-024-01190-6

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2
African ancestry-derived APOL1 risk genotypes show proximal epigenetic associations
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African ancestry-derived APOL1 risk genotypes show proximal epigenetic associations

BMC genomics, 2024-05, Vol.25 (1), p.452-452 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;ISSN: 1471-2164 ;EISSN: 1471-2164 ;DOI: 10.1186/s12864-024-10226-0 ;PMID: 38714935

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3
Age Prediction Using DNA Methylation Heterogeneity Metrics
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Age Prediction Using DNA Methylation Heterogeneity Metrics

International journal of molecular sciences, 2024-05, Vol.25 (9), p.4967 [Peer Reviewed Journal]

COPYRIGHT 2024 MDPI AG ;2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25094967 ;PMID: 38732187

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4
A chromosome-scale fishing cat reference genome for the evaluation of potential germline risk variants
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A chromosome-scale fishing cat reference genome for the evaluation of potential germline risk variants

Scientific reports, 2024-04, Vol.14 (1), p.8073-8073 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-56003-7 ;PMID: 38580653

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5
The association between serum methylmalonic acid, cobalamin-related biomarkers, and long-term mortality risk in cancer survivors: a prospective cohort study
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The association between serum methylmalonic acid, cobalamin-related biomarkers, and long-term mortality risk in cancer survivors: a prospective cohort study

The American journal of clinical nutrition, 2024-05, Vol.119 (5), p.1122-1132 [Peer Reviewed Journal]

2024 American Society for Nutrition ;Copyright © 2024 American Society for Nutrition. Published by Elsevier Inc. All rights reserved. ;Copyright American Society for Clinical Nutrition, Inc. May 2024 ;ISSN: 0002-9165 ;EISSN: 1938-3207 ;DOI: 10.1016/j.ajcnut.2024.02.009 ;PMID: 38702109

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6
Integrating population genetics, stem cell biology and cellular genomics to study complex human diseases
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Integrating population genetics, stem cell biology and cellular genomics to study complex human diseases

Nature genetics, 2024-05, Vol.56 (5), p.758-766 [Peer Reviewed Journal]

2024. Springer Nature America, Inc. ;Copyright Nature Publishing Group May 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01731-9 ;PMID: 38741017

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7
Protein-altering variants at copy number-variable regions influence diverse human phenotypes
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Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Nature genetics, 2024-04, Vol.56 (4), p.569-2 [Peer Reviewed Journal]

2024. The Author(s). ;Copyright Nature Publishing Group Apr 2024 ;The Author(s) 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01684-z ;PMID: 38548989

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8
Using genome and transcriptome data from African-ancestry female participants to identify putative breast cancer susceptibility genes
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Using genome and transcriptome data from African-ancestry female participants to identify putative breast cancer susceptibility genes

Nature communications, 2024-05, Vol.15 (1), p.3718-3718 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-47650-5 ;PMID: 38697998

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9
Phenome-wide Mendelian randomisation analysis of 378,142 cases reveals risk factors for eight common cancers
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Phenome-wide Mendelian randomisation analysis of 378,142 cases reveals risk factors for eight common cancers

Nature communications, 2024-03, Vol.15 (1), p.2637-2637 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-46927-z ;PMID: 38527997

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10
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
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Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes

Nature communications, 2024, Vol.15 (1), p.3557-3557 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-47399-x ;PMID: 38670944

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11
Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction
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Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction

Nature genetics, 2024-05, Vol.56 (5), p.819-3 [Peer Reviewed Journal]

2024. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group May 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01736-4 ;PMID: 38741014

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12
Cell-type-specific and disease-associated expression quantitative trait loci in the human lung
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Cell-type-specific and disease-associated expression quantitative trait loci in the human lung

Nature genetics, 2024-04, Vol.56 (4), p.595-3 [Peer Reviewed Journal]

2024. The Author(s). ;Copyright Nature Publishing Group Apr 2024 ;The Author(s) 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01702-0 ;PMID: 38548990

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13
The 1+Million Genomes Minimal Dataset for Cancer
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The 1+Million Genomes Minimal Dataset for Cancer

Nature genetics, 2024-05, Vol.56 (5), p.733-736 [Peer Reviewed Journal]

Copyright Nature Publishing Group May 2024 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01721-x ;PMID: 38702538

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14
Rheumatoid arthritis and idiopathic pulmonary fibrosis: a bidirectional Mendelian randomisation study
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Rheumatoid arthritis and idiopathic pulmonary fibrosis: a bidirectional Mendelian randomisation study

Thorax, 2024-04, Vol.79 (6), p.538-544 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. 2024 ;ISSN: 0040-6376 ;EISSN: 1468-3296 ;DOI: 10.1136/thorax-2023-220856 ;PMID: 38649271

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15
Spatial-temporal transmission dynamics of HIV-1 CRF01_AE in Indonesia
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Spatial-temporal transmission dynamics of HIV-1 CRF01_AE in Indonesia

Scientific reports, 2024-05, Vol.14 (1), p.9917-9917 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-59820-y ;PMID: 38730038

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16
Genetically identification of endometriosis and cancers risk in women through a two-sample Mendelian randomization study
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Genetically identification of endometriosis and cancers risk in women through a two-sample Mendelian randomization study

Scientific reports, 2024-04, Vol.14 (1), p.8382-8382 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-58950-7 ;PMID: 38600147

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17
Ensemble learning for integrative prediction of genetic values with genomic variants
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Ensemble learning for integrative prediction of genetic values with genomic variants

BMC bioinformatics, 2024-03, Vol.25 (1), p.120-120 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;ISSN: 1471-2105 ;EISSN: 1471-2105 ;DOI: 10.1186/s12859-024-05720-x ;PMID: 38515026

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18
Genetic regulation of cell type-specific chromatin accessibility shapes brain disease etiology
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Genetic regulation of cell type-specific chromatin accessibility shapes brain disease etiology

Science (American Association for the Advancement of Science), 2024-05, Vol.384 (6698), p.eadh4265-eadh4265 [Peer Reviewed Journal]

Copyright © 2024 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.adh4265 ;PMID: 38781378

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19
Molecular characterization of emerging Echovirus 11 (E11) shed light on the recombinant origin of a variant associated with severe hepatitis in neonates
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Molecular characterization of emerging Echovirus 11 (E11) shed light on the recombinant origin of a variant associated with severe hepatitis in neonates

Journal of medical virology, 2024-05, Vol.96 (5), p.e29658 [Peer Reviewed Journal]

2024 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC. ;EISSN: 1096-9071 ;DOI: 10.1002/jmv.29658 ;PMID: 38727043

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20
Changes in intrahost genetic diversity according to lesion severity in longitudinal HPV16 samples
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Article
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Changes in intrahost genetic diversity according to lesion severity in longitudinal HPV16 samples

Journal of medical virology, 2024-05, Vol.96 (5), p.e29641 [Peer Reviewed Journal]

2024 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC. ;EISSN: 1096-9071 ;DOI: 10.1002/jmv.29641 ;PMID: 38708811

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