Gail P. Clement

发表

Introducing Digital Object Identifiers (DOIs) and their value for Researchers: An AuthorCarpentry Lesson

Gail P. Clement, 2016 .

Sharing Research Openly with Creative Commons: An AuthorCarpentry Lesson

Gail P. Clement, 2016 .

Open Citations, BibTeX Format & Populating an ORCiD Profile: An AuthorCarpentry Lesson

Gail P. Clement, 2016 .

The UK10K project identifies rare variants in health and disease

Tom R. Gaunt, Hashem A. Shihab, Gail P. Clement, 2016 .

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.

Gail Clement, Gail P. Clement, Greg Gibson, 2009, Human molecular genetics.

JLSC Board Editorial 2018

Gail P. Clement, Danny Kingsley, S. Searle, 2018, Journal of Librarianship and Scholarly Communication.

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2017, Scientific Reports.

Universitet Low-frequency variation in TP 53 has large effects on head circumference and intracranial

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2019 .

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

Tom R. Gaunt, Hashem A. Shihab, Gail P. Clement, 2018, bioRxiv.

Choline-stabilized orthosilicic acid supplementation as an adjunct to Calcium/Vitamin D3 stimulates markers of bone formation in osteopenic females: a randomized, placebo-controlled trial

Gail P. Clement, T. Spector, J. Powell, 2008, BMC musculoskeletal disorders.

Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2019, Nature Communications.

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

Gail Clement, Jie Huang, Antonio Ciampi, 2014, Nature Communications.

Toward the Geoscience Paper of the Future: Best practices for documenting and sharing research from data to software to provenance

Gail Clement, Gail P. Clement, 2017 .

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2018, bioRxiv.

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Tom R. Gaunt, Klaudia Walter, Nicholas J Timpson, 2015, Nature Communications.

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2017, Scientific Reports.

UK 10 K Consortium

Tom R. Gaunt, Hashem A. Shihab, Gail P. Clement, 2019 .

Heritability analyses show visit-to-visit blood pressure variability reflects different pathological phenotypes in younger and older adults: evidence from UK twins

Gail P. Clement, T. Spector, M. Mangino, 2013, Journal of hypertension.

The Basis of Differential Responses to Folic Acid Supplementation

Gail P. Clement, G. Surdulescu, K. Ahmadi, 2011, Lifestyle Genomics.

Genetic epidemiology of induced CYP3A4 activity

Gail P. Clement, G. Surdulescu, K. Ahmadi, 2011, Pharmacogenetics and genomics.

The interaction of genes and smoking on forced expiratory volume: a classic twin study.

Gail P. Clement, T. Spector, D. Strachan, 2007, Chest.

A Twin Study of Mitochondrial DNA Polymorphisms Shows that Heteroplasmy at Multiple Sites Is Associated with mtDNA Variant 16093 but Not with Zygosity

Gail P. Clement, T. Spector, P. Chowienczyk, 2011, PloS one.

Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Gail Clement, Jie Huang, Inês Barroso, 2016, Nature Communications.

From the Ground Up: A Group Editorial on the Most Pressing Issues in Scholarly Communication

Gail Clement, Nicky Agate, Leah Vanderjagt, 2017 .

ETD Management and Publishing in the ProQuest System and the University Repository: A Comparative Analysis

Gail Clement, Fred Rascoe, Gail P. Clement, 2013 .

The UK10K project identifies rare variants in health and disease

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2015, Nature.

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Tom R. Gaunt, Thomas M. Keane, Colin A. Johnson, 2015, Nature Communications.

Sequencing of SCN5A Identifies Rare and Common Variants Associated With Cardiac Conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Tom R. Gaunt, Gail P. Clement, Shane A. McCarthy, 2014, Circulation. Cardiovascular genetics.

Collecting and Digitizing Forgotten Graduate Student Scholarship: The PILOs Project at Texas A&M University

Sarah Potvin, Sandra L. Tucker, Violeta Ilik, 2014 .

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2015, Nature Communications.

Choline-stabilized orthosilicic acid supplementation as an adjunct to Calcium/Vitamin D3 stimulates markers of bone formation in osteopenic females: a randomized, placebo-controlled trial

Gail P. Clement, T. Spector, J. Powell, 2008, BMC musculoskeletal disorders.

Establishing Your Scholarly/Professional Identity with ORCID: A Care and Feeding Manual for Graduate Students

Gail Clement, Gail P. Clement, 2014 .

ORCID Identifiers: Planned and Potential Uses by Associations, Publishers, and Librarians

Gail Clement, Gail P. Clement, Wm. Joseph Thomas, 2015 .