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Reflection in Learning & Professional Development: Theory & Practice

Moon, Jennifer A

1999

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Developing a Culture of Mentorship to Strengthen Academic Medical Centers

Academic medicine, 2019-05, Vol.94 (5), p.630-633

2019

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PIF1 directly and indirectly regulates chlorophyll biosynthesis to optimize the greening process in Arabidopsis

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (27), p.9433-9438

2008

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Chromosome silencing in vitro reveals trisomy 21 causes cell-autonomous deficits in angiogenesis and early dysregulation in Notch signaling

Cell reports (Cambridge), 2022-08, Vol.40 (6), p.111174-111174, Article 111174

2022

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The Ubiquitin-Proteasome Pathway and Plant Development

The Plant cell, 2004-12, Vol.16 (12), p.3181-3195

2004

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Management of Cardiovascular Risk: The Importance of Meeting Lipid Targets

The American journal of cardiology, 2012-07, Vol.110 (1), p.3A-14A

2012

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Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature

Human mutation, 2015-04, Vol.36 (4), p.474-481

2015

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Evaluation of Lipids, Drug Concentration, and Safety Parameters Following Cessation of Treatment With the Cholesteryl Ester Transfer Protein Inhibitor Anacetrapib in Patients With or at High Risk for Coronary Heart Disease

The American journal of cardiology, 2014, Vol.113 (1), p.76-83

2014

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PIF1 is regulated by light-mediated degradation through the ubiquitin-26S proteasome pathway to optimize photomorphogenesis of seedlings in Arabidopsis

The Plant journal : for cell and molecular biology, 2005-12, Vol.44 (6), p.1023-1035

2005

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Recent Clinical Studies of the Effects of Lipid-Modifying Therapies

The American journal of cardiology, 2012-07, Vol.110 (1), p.15A-26A

2012

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Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity

Nature genetics, 2015-08, Vol.47 (8), p.921-925

2015

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Pharmacotherapies for lipid modification: beyond the statins

Nature reviews cardiology, 2013-10, Vol.10 (10), p.560-570

2013

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Whole Exome Sequencing to Identify Genetic Causes of Short Stature

Hormone research in paediatrics, 2014-01, Vol.82 (1), p.44-52

2014

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Meeting the challenges of medical student mental health and well‐being today

Medical education, 2020-03, Vol.54 (3), p.183-185

2020

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The Neuropsychology of Down Syndrome: Evidence for Hippocampal Dysfunction

Child development, 2003-01, Vol.74 (1), p.75-93

2003

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A Novel Deletion of IGF1 in a Patient With Idiopathic Short Stature Provides Insight Into IGF1 Haploinsufficiency

The journal of clinical endocrinology and metabolism, 2014-01, Vol.99 (1), p.E153-E159

2014

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Large-Scale Pooled Next-Generation Sequencing of 1077 Genes to Identify Genetic Causes of Short Stature

The journal of clinical endocrinology and metabolism, 2013-08, Vol.98 (8), p.E1428-E1437

2013

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Novel Microcephalic Primordial Dwarfism Disorder Associated with Variants in the Centrosomal Protein Ninein

The journal of clinical endocrinology and metabolism, 2012-11, Vol.97 (11), p.E2140-E2151

2012

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Novel germline mutation (Leu512Met) in the thyrotropin receptor gene (TSHR) leading to sporadic non-autoimmune hyperthyroidism

Journal of Pediatric Endocrinology and Metabolism, 2017-03, Vol.30 (3), p.343

2017

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Weill Cornell Medicine: A History of Cornell’s Medical School

1, 2016

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Safety of inhibition of cholesteryl ester transfer protein with anacetrapib: the DEFINE study

Expert review of cardiovascular therapy, 2012-08, Vol.10 (8), p.955-963

2012

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Lipids, Safety Parameters, and Drug Concentrations After an Additional 2 Years of Treatment With Anacetrapib in the DEFINE Study

Journal of cardiovascular pharmacology and therapeutics, 2014-11, Vol.19 (6), p.543-549

2014

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New CULLIN 1 Mutant Has Altered Responses to Hormones and Light in Arabidopsis

Plant physiology (Bethesda), 2007-02, Vol.143 (2), p.684-696

2007

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Short Courses & Workshops: Improving the Impact of Learning, Training & Professional Development

Moon, Jennifer

2001

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Functional Significance of Single Nucleotide Polymorphisms in the Lactase Gene in Diverse US Patients and Evidence for a Novel Lactase Persistence Allele at −13909 in Those of European Ancestry

Journal of pediatric gastroenterology and nutrition, 2015-02, Vol.60 (2), p.182-191

2015

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Reflection in Learning & Professional Development: Theory & Practice

Developing a Culture of Mentorship to Strengthen Academic Medical Centers

PIF1 directly and indirectly regulates chlorophyll biosynthesis to optimize the greening process in Arabidopsis

Chromosome silencing in vitro reveals trisomy 21 causes cell-autonomous deficits in angiogenesis and early dysregulation in Notch signaling

The Ubiquitin-Proteasome Pathway and Plant Development

Management of Cardiovascular Risk: The Importance of Meeting Lipid Targets

Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature

Evaluation of Lipids, Drug Concentration, and Safety Parameters Following Cessation of Treatment With the Cholesteryl Ester Transfer Protein Inhibitor Anacetrapib in Patients With or at High Risk for Coronary Heart Disease

PIF1 is regulated by light-mediated degradation through the ubiquitin-26S proteasome pathway to optimize photomorphogenesis of seedlings in Arabidopsis

Recent Clinical Studies of the Effects of Lipid-Modifying Therapies

Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity

Pharmacotherapies for lipid modification: beyond the statins

Whole Exome Sequencing to Identify Genetic Causes of Short Stature

Meeting the challenges of medical student mental health and well‐being today

The Neuropsychology of Down Syndrome: Evidence for Hippocampal Dysfunction

A Novel Deletion of IGF1 in a Patient With Idiopathic Short Stature Provides Insight Into IGF1 Haploinsufficiency

Large-Scale Pooled Next-Generation Sequencing of 1077 Genes to Identify Genetic Causes of Short Stature

Novel Microcephalic Primordial Dwarfism Disorder Associated with Variants in the Centrosomal Protein Ninein

Novel germline mutation (Leu512Met) in the thyrotropin receptor gene (TSHR) leading to sporadic non-autoimmune hyperthyroidism

Weill Cornell Medicine: A History of Cornell’s Medical School

Safety of inhibition of cholesteryl ester transfer protein with anacetrapib: the DEFINE study

Lipids, Safety Parameters, and Drug Concentrations After an Additional 2 Years of Treatment With Anacetrapib in the DEFINE Study

New CULLIN 1 Mutant Has Altered Responses to Hormones and Light in Arabidopsis

Short Courses & Workshops: Improving the Impact of Learning, Training & Professional Development

Functional Significance of Single Nucleotide Polymorphisms in the Lactase Gene in Diverse US Patients and Evidence for a Novel Lactase Persistence Allele at −13909 in Those of European Ancestry

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