Publications by authors named "Allan Daly"

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Alzheimer's disease medication use and adherence patterns by race and ethnicity.
Natalia Olchanski, Allan T Daly, Yingying Zhu, Rachel Breslau, Joshua T Cohen

Alzheimers Dement· April 2023

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Low-Value Prostate-Specific Antigen Test for Prostate Cancer Screening and Subsequent Health Care Utilization and Spending.
David D Kim, Allan T Daly, Benjamin C Koethe, A Mark Fendrick, Daniel A Ollendorf

JAMA Netw Open· November 2022

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Cost-effectiveness of DPYD Genotyping Prior to Fluoropyrimidine-based Adjuvant Chemotherapy for Colon Cancer.
Gabriel A Brooks, Stephanie Tapp, Allan T Daly, Jonathan A Busam, Anna N A Tosteson

Clin Colorectal Cancer· September 2022

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Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.
Aleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, Kai Yuan, Brandon Avila, Allan Daly, Mark J Daly

Nat Genet· September 2022

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State-Level Variation In Low-Value Care For Commercially Insured And Medicare Advantage Populations.
Lauren A Do, Benjamin C Koethe, Allan T Daly, James D Chambers, Daniel A Ollendorf

Health Aff (Millwood)· September 2022

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An Evidence Review of Low-Value Care Recommendations: Inconsistency and Lack of Economic Evidence Considered.
David D Kim, Lauren A Do, Allan T Daly, John B Wong, James D Chambers

J Gen Intern Med· November 2021

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Dementia Diagnosis Disparities by Race and Ethnicity.
Pei-Jung Lin, Allan T Daly, Natalia Olchanski, Joshua T Cohen, Peter J Neumann

Med Care· August 2021

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Racial and Ethnic Differences in Knowledge About One's Dementia Status.
Pei-Jung Lin, Joanna Emerson, Jessica D Faul, Joshua T Cohen, Peter J Neumann, Allan T Daly

J Am Geriatr Soc· August 2020

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Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription.
Gaëlle Marenne, Audrey E Hendricks, Aliki Perdikari, Rebecca Bounds, Felicity Payne, Allan Daly

Cell Metab· June 2020

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Cost-effectiveness analysis of smoking cessation interventions using cell phones in a low-income population.
Allan T Daly, Ashish A Deshmukh, Damon J Vidrine, Alexander V Prokhorov, Summer G Frank

Tob Control· January 2019

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Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutations.
Isabel Huang-Doran, Patsy Tomlinson, Felicity Payne, Alexandra Gast, Alison Sleigh, Allan Daly

JCI Insight· October 2016

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Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Allan Daly

Nat Genet· September 2016

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Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient.
Eleanor Raffan, Liam A Hurst, Saeed Al Turki, Gillian Carpenter, Carol Scott, Allan Daly

Front Endocrinol (Lausanne)· August 2012

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Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA.
Marjorie J Lindhurst, Victoria E R Parker, Felicity Payne, Julie C Sapp, Simon Rudge, Allan Daly

Nat Genet· June 2012

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Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk.
Katherine A Fawcett, Eleanor Wheeler, Andrew P Morris, Sally L Ricketts, Göran Hallmans, Allan Daly

Diabetes· March 2010

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Population differentiation as an indicator of recent positive selection in humans: an empirical evaluation.
Yali Xue, Xuelong Zhang, Ni Huang, Allan Daly, Christopher J Gillson

Genetics· November 2009

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Variation of the oxytocin/neurophysin I (OXT) gene in four human populations.
Yang Xu, Yali Xue, Asan, Allan Daly, Lijie Wu

J Hum Genet· September 2008

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Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations.
Katherine A Fawcett, Neil Grimsey, Ruth J F Loos, Eleanor Wheeler, Allan Daly

Diabetes· September 2008

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Adaptive evolution of UGT2B17 copy-number variation.
Yali Xue, Donglin Sun, Allan Daly, Fengtang Yang, Xue Zhou

Am J Hum Genet· September 2008

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Common variants in WFS1 confer risk of type 2 diabetes.
Manjinder S Sandhu, Michael N Weedon, Katherine A Fawcett, Jon Wasson, Sally L Debenham, Allan Daly

Nat Genet· August 2007

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Spread of an inactive form of caspase-12 in humans is due to recent positive selection.
Yali Xue, Allan Daly, Bryndis Yngvadottir, Mengning Liu, Graham Coop

Am J Hum Genet· April 2006

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