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Is there a place for undergraduate and graduate students in the systematic review process?

Journal of the Medical Library Association, 2018-04, Vol.106 (2), p.248-250

Wissinger, Christina L

2018

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Privacy Literacy: From Theory to Practice

Communications in information literacy, 2017-01, Vol.11 (2), p.378-389

Wissinger, Christina

2017

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Using the Extended Parallel Process Model to Frame E-Professionalism Instruction in Healthcare Education

Teaching and learning in medicine, 2019-05, Vol.31 (3), p.335-341

2019

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Expert Teams in the Academic Library: Going Beyond Subject Expertise to Create Scaffolded Instruction

Journal of library administration, 2018-05, Vol.58 (4), p.313-333

2018

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It’s Not Where You Start or Where You Finish - It’s How You Get There

Pennsylvania libraries, 2021-12, Vol.9 (2), p.74-78

2021

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Physical Examination-Indicated Cerclage: A Systematic Review and Meta-analysis

Obstetrics and gynecology (New York. 1953), 2015-07, Vol.126 (1), p.125-135

2015

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152: Physical exam indicated cerclage versus expectant management: a systematic review and metaanalysis

American journal of obstetrics and gynecology, 2013, Vol.208 (1), p.S76-S76

2013

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Editorial Responsibilities

Evidence based library and information practice, 2019-01, Vol.14 (3), p.1-1

., .

2019

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The language of privacy and power in social media: A quantitative analysis of ambiguous content in privacy policies

Wissinger, Christina L

2016

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Student Perceptions of Facebook’s Privacy Policies & Rights

Journal of Social Media Studies, 2015-06, Vol.2 (1), p.15-26

Wissinger, Christina L.

2015

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Beyond the lab: Virtual reality for undergraduate Anatomy and Physiology students

College & Research Libraries News, 2021-04, Vol.82 (4), p.186

2021

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Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

PloS one, 2016-01, Vol.11 (1), p.e0145951-e0145951

2016

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A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

American journal of human genetics, 2012-09, Vol.91 (3), p.527-532

2012

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Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy

American journal of human genetics, 2006-11, Vol.79 (5), p.973-977

2006

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Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

Nature genetics, 2004-08, Vol.36 (8), p.850-854

2004

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

American journal of human genetics, 2012-02, Vol.90 (2), p.321-330

2012

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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

American journal of human genetics, 2006-10, Vol.79 (4), p.657-667

2006

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Nature genetics, 2000-11, Vol.26 (3), p.324-327

2000

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Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy

The Journal of clinical investigation, 2018-12, Vol.128 (12), p.5663-5675

2018

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Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F‐mediated inherited retinal disorders

Human mutation, 2019-06, Vol.40 (6), p.765-787

2019

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Targeted Ablation of the Pde6h Gene in Mice Reveals Cross-species Differences in Cone and Rod Phototransduction Protein Isoform Inventory

The Journal of biological chemistry, 2015-04, Vol.290 (16), p.10242-10255

2015

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Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration

Human molecular genetics, 2005-01, Vol.14 (2), p.255-265

2005

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Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle

Human molecular genetics, 2005-12, Vol.14 (24), p.3865-3875

2005

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Is there a place for undergraduate and graduate students in the systematic review process?

Privacy Literacy: From Theory to Practice

Using the Extended Parallel Process Model to Frame E-Professionalism Instruction in Healthcare Education

Expert Teams in the Academic Library: Going Beyond Subject Expertise to Create Scaffolded Instruction

It’s Not Where You Start or Where You Finish - It’s How You Get There

Physical Examination-Indicated Cerclage: A Systematic Review and Meta-analysis

152: Physical exam indicated cerclage versus expectant management: a systematic review and metaanalysis

Editorial Responsibilities

The language of privacy and power in social media: A quantitative analysis of ambiguous content in privacy policies

Student Perceptions of Facebook’s Privacy Policies & Rights

Beyond the lab: Virtual reality for undergraduate Anatomy and Physiology students

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy

Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy

CNGB1‐related rod‐cone dystrophy: A mutation review and update

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F‐mediated inherited retinal disorders

Targeted Ablation of the Pde6h Gene in Mice Reveals Cross-species Differences in Cone and Rod Phototransduction Protein Isoform Inventory

Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration

Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle

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