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A Primer on Bayesian Inference for Biophysical Systems

Biophysical journal, 2015-05, Vol.108 (9), p.2103-2113

Hines, Keegan E.

2015

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Determination of parameter identifiability in nonlinear biophysical models: A Bayesian approach

The Journal of general physiology, 2014-03, Vol.143 (3), p.401-416

2014

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Inferring subunit stoichiometry from single molecule photobleaching

The Journal of general physiology, 2013-06, Vol.141 (6), p.737-746

Hines, Keegan E

2013

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Insights into DNA-binding motifs and mechanisms of Francisella tularensis novicida two-component system response regulator proteins QseB, KdpE, and BfpR

Biochemical and biophysical research communications, 2024-08, Vol.722, p.150150, Article 150150

2024

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Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis

International journal of molecular sciences, 2021-04, Vol.22 (9), p.4448

2021

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Analyzing Single-Molecule Time Series via Nonparametric Bayesian Inference

Biophysical journal, 2015-02, Vol.108 (3), p.540-556

2015

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Becoming a birth mother in the context of a planned same-sex family: 'As amazing as it is, it's kind of a tough road to navigate'

Journal of family studies, 2023-03, Vol.29 (2), p.807-823

2023

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Periurethral injection therapy for urinary incontinence in women

Cochrane database of systematic reviews, 2007-01 (3), p.CD003881

2007

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Genotype-phenotype analysis of 523 patients by genetics evaluation and clinical exome sequencing

Pediatric research, 2020-03, Vol.87 (4), p.735-739

2020

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Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability

Frontiers in molecular neuroscience, 2018-04, Vol.11, p.104-104

2018

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Winter Rye Cover Crop Impacts on Runoff Water Quality in a Northern New York (USA) Tile-Drained Maize Agroecosystem

Water, air, and soil pollution, 2020-02, Vol.231 (2), Article 84

2020

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Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia

American journal of human genetics, 2003-02, Vol.72 (2), p.408-418

2003

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Telomere Protection by TPP1 Is Mediated by POT1a and POT1b

Molecular and Cellular Biology, 2010-02, Vol.30 (4), p.1059-1066

2010

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Genetics of Bladder-Exstrophy-Epispadias Complex (BEEC): Systematic Elucidation of Mendelian and Multifactorial Phenotypes

Current genomics, 2016-02, Vol.17 (1), p.4-13

2016

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Trauma as a Public Health Moment: Addressing Vaccine Uptake in Trauma Patients

Annals of surgery open, 2023-12, Vol.4 (4), p.e356-e356

2023

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A chromatin remodelling SWI/SNF subunit, Snr1, regulates neural stem cell determination and differentiation

Development (Cambridge), 2023-07, Vol.150 (13)

2023

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Urethral injection therapy for urinary incontinence in women

Cochrane database of systematic reviews, 2017-07, Vol.7 (7), p.CD003881

2017

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TPP1 mutagenesis screens unravel shelterin interfaces and functions in hematopoiesis

JCI insight, 2021-05, Vol.6 (9)

2021

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An Interdisciplinary Approach to Müllerian Outflow Tract Obstruction Associated with Cloacal Malformation and Cloacal Exstrophy

Journal of clinical medicine, 2022-07, Vol.11 (15), p.4408

2022

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Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1

Genes & development, 2014-10, Vol.28 (19), p.2090-2102

2014

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Urethral injection therapy for urinary incontinence in women

Cochrane database of systematic reviews, 2012-02 (2), p.CD003881

2012

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Identification of critical regions for clinical features of distal 10q deletion syndrome

Clinical genetics, 2009-07, Vol.76 (1), p.54-62

2009

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Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes

Genetics in medicine, 2008-04, Vol.10 (4), p.267-277

2008

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Next-generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression

PLoS genetics, 2013-02, Vol.9 (2), p.e1003205

2013

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Recent insights into organogenesis of the adrenal cortex

Trends in Endocrinology & Metabolism, 2002-07, Vol.13 (5), p.200-208

2002

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A Primer on Bayesian Inference for Biophysical Systems

Determination of parameter identifiability in nonlinear biophysical models: A Bayesian approach

Inferring subunit stoichiometry from single molecule photobleaching

Insights into DNA-binding motifs and mechanisms of Francisella tularensis novicida two-component system response regulator proteins QseB, KdpE, and BfpR

Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis

Analyzing Single-Molecule Time Series via Nonparametric Bayesian Inference

Becoming a birth mother in the context of a planned same-sex family: 'As amazing as it is, it's kind of a tough road to navigate'

Periurethral injection therapy for urinary incontinence in women

Genotype-phenotype analysis of 523 patients by genetics evaluation and clinical exome sequencing

Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability

Winter Rye Cover Crop Impacts on Runoff Water Quality in a Northern New York (USA) Tile-Drained Maize Agroecosystem

Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia

Telomere Protection by TPP1 Is Mediated by POT1a and POT1b

Genetics of Bladder-Exstrophy-Epispadias Complex (BEEC): Systematic Elucidation of Mendelian and Multifactorial Phenotypes

Trauma as a Public Health Moment: Addressing Vaccine Uptake in Trauma Patients

A chromatin remodelling SWI/SNF subunit, Snr1, regulates neural stem cell determination and differentiation

Urethral injection therapy for urinary incontinence in women

TPP1 mutagenesis screens unravel shelterin interfaces and functions in hematopoiesis

An Interdisciplinary Approach to Müllerian Outflow Tract Obstruction Associated with Cloacal Malformation and Cloacal Exstrophy

Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1

Urethral injection therapy for urinary incontinence in women

Identification of critical regions for clinical features of distal 10q deletion syndrome

Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes

Next-generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression

Recent insights into organogenesis of the adrenal cortex

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