Citation Impact
Citing Papers
TFEB Links Autophagy to Lysosomal Biogenesis
2011 StandoutScience
Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy
2010 StandoutScience
Impairment of starvation-induced and constitutive autophagy in Atg7 -deficient mice
2005 StandoutNobel
2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease
2014 Standout
2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer
2015 Standout
AIF meets the CHCHD4/Mia40-dependent mitochondrial import pathway
2020
Acromegaly
2006 Standout
Molecular genetics of congenital nuclear cataract
2014
Kidney stones: pathophysiology and medical management
2006 Standout
Myopia
2012 Standout
Gout-associated uric acid crystals activate the NALP3 inflammasome
2006 StandoutNature
Deletion of Autophagy-related 5 (Atg5) and Pik3c3 Genes in the Lens Causes Cataract Independent of Programmed Organelle Degradation
2013
Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia
2004
Risk Factors for Hospital-Acquired Staphylococcus aureus Bacteremia
1999
Autoinflammatory Disease Reloaded: A Clinical Perspective
2010 Standout
Clinical and molecular aspects of adrenocortical tumourigenesis
2003
Excess Length of Stay, Charges, and Mortality Attributable to Medical Injuries During Hospitalization
2003 Standout
Cushing's syndrome
2015 Standout
Guidelines on Prevention, Diagnosis and Treatment of Infective Endocarditis Executive Summary The Task Force on Infective Endocarditis of the European Society of Cardiology
2004 Standout
Abnormal Adrenal and Vascular Responses to Vasopressin Mediated by a V1-Vasopressin Receptor in a Patient with Adrenocorticotropin-Independent Macronodular Adrenal Hyperplasia, Cushing’s Syndrome, and Orthostatic Hypotension1
1997
Candida tropicalis Pacemaker Endocarditis
2000
Paediatric Cushing's syndrome: epidemiology, investigation and therapeutic advances
2007
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex
2000 Standout
Cyclical Cushing Syndrome Presenting in Infancy: An Early Form of Primary Pigmented Nodular Adrenocortical Disease, or a New Entity?
2004
Diagnostic and treatment concerns in familial Mediterranean fever
2000
Infective Endocarditis—A Prospective Study at the End of the Twentieth Century
2001
Nosocomial cardiac infections
2002
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
Epidemiology of Acromegaly
1999
Decoding ALS: from genes to mechanism
2016 StandoutNature
Pacemaker Endocarditis: Clinical Features and Management of 60 Consecutive Cases
2007
mTOR Signaling in Growth, Metabolism, and Disease
2017 Standout
Infective Endocarditis Complicating Permanent Pacemaker and Implantable Cardioverter-Defibrillator Infection
2008
Pacemaker infective endocarditis
1998
Update on Cardiovascular Implantable Electronic Device Infections and Their Management
2010
Retinitis pigmentosa
2006 Standout
Clinical disease among patients heterozygous for familial mediterranean fever
2009
Characterization of a Mutation in the Lens-specific MP70 Encoding Gene of the Mouse Leading to a Dominant Cataract
2001
cAMP/PKA signaling defects in tumors: Genetics and tissue-specific pluripotential cell-derived lesions in human and mouse
2013
Genome‐scale identification of UDP‐GlcNAc‐dependent pathways
2008
The CEPH Consortium Linkage Map of Human Chromosome 13
1993
Primary Pigmented Nodular Adrenocortical Disease: Reevaluation of a Patient with Carney Complex 27 Years after Unilateral Adrenalectomy
1997
Spondylodiscitis Associated with Bacteraemia due to Coagulase-Negative Staphylococci
2000
Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever
1997
Familial Mediterranean fever in three Japanese patients, and a comparison of the frequency of MEFV gene mutations in Japanese and Mediterranean populations
2007
Vertebral Osteomyelitis
2010 Standout
p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataract
2013
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
The Inflammasomes
2010 Standout
The Amyloid State of Proteins in Human Diseases
2012 Standout
Mechanisms for pituitary tumorigenesis: the plastic pituitary
2003
A Large Family with Carney Complex Caused by the S147G PRKAR1A Mutation Shows a Unique Spectrum of Disease Including Adrenocortical Cancer
2011
AKT/PKB Signaling: Navigating the Network
2017 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Ferroptosis: mechanisms, biology and role in disease
2021 Standout
Cushing's syndrome
2006 Standout
The Hallmarks of Aging
2013 Standout
Points of control in inflammation
2002 StandoutNature
Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complex
2000
The TNF and TNF Receptor Superfamilies
2001 Standout
Infections of intracardiac devices
2003
Pacemaker Endocarditis Due to Candida albicans: Case Report and Review
1997
Autoimmunity and Apoptosis
2001 StandoutNobel
Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update
2010
Infective endocarditis
2004 Standout
TMEM41B Is a Pan-flavivirus Host Factor
2020 StandoutNobel
The epidemiology and genetics of pituitary adenomas
2009
Molecular Mechanisms of Amyloidosis
2003 Standout
TNFRSF1A mutations and autoinflammatory syndromes
2000
Familial Syndromes Associated with Thyroid Cancer in the Era of Personalized Medicine
2010
TBC1D20 mediates autophagy as a key regulator of autophagosome maturation
2016
Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (PRKAR1A): Phenotype Analysis in 353 Patients and 80 Different Genotypes
2009
Candida Infections of Medical Devices
2004 Standout
Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci
1998
Metabolic cross-talk allows labeling of O-linked β- N -acetylglucosamine-modified proteins via the N -acetylgalactosamine salvage pathway
2011 StandoutNobel
Clinical Characteristics and Outcome of Infective Endocarditis Involving Implantable Cardiac Devices
2012
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991 Standout
Autosomal Recessive Retinitis Pigmentosa Is Associated with Mutations inRP1in Three Consanguineous Pakistani Families
2005
Molecular and functional analysis of PRKAR1A and its locus (17q22-24) in sporadic adrenocortical tumors: 17q losses, somatic mutations, and protein kinase A expression and activity.
2003
The Heritability of Ocular Traits
2010
Familial Mediterranean fever in three Japanese patients, and a comparison of the frequency ofMEFVgene mutations in Japanese and Mediterranean populations
2008
An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma
2001
Membrane proteomics of phagosomes suggests a connection to autophagy
2008 StandoutNobel
The amino acid transport system bo,+and cystinuria
2001
Adrenocortical Overexpression of Gastric Inhibitory Polypeptide Receptor Underlies Food-Dependent Cushing’s Syndrome1
1998
Fluorescence Lifetime Measurements and Biological Imaging
2010 Standout
PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein
1996 StandoutScience
Diagnosis and Management of Infections Involving Implantable Electrophysiologic Cardiac Devices
2000
Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient Evaluation
2001
The Diagnosis and Differential Diagnosis of Cushing’s Syndrome and Pseudo-Cushing’s States
1998
ACC/AHA 2006 Guidelines for the Management of Patients With Valvular Heart Disease
2006 Standout
Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes
2000
Primary Pigmented Nodular Adrenocortical Disease: Paradoxical Responses of Cortisol Secretion to Dexamethasone Occur in Vitro and Are Associated with Increased Expression of the Glucocorticoid Receptor
2003
Nonvalvular Cardiovascular Device–Related Infections
2003
Paradoxical Response to Dexamethasone in the Diagnosis of Primary Pigmented Nodular Adrenocortical Disease
1999
Cataracts
2017 Standout
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
2004
Cloning and characterization of a functional human homolog of Escherichia coli endonuclease III
1997 StandoutNobel
The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16
1994
Genetics of Congenital Cataract
2016
The diversity of abnormal hormone receptors in adrenal Cushing's syndrome allows novel pharmacological therapies
2000
Identification of a Novel Genetic Locus for Familial Cardiac Myxomas and Carney Complex
1998
Membrane Morphology Is Actively Transformed by Covalent Binding of the Protein Atg8 to PE-Lipids
2014 StandoutNobel
Ectopic and Abnormal Hormone Receptors in Adrenal Cushing’s Syndrome*
2001
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
2009 StandoutScience
SMART, a simple modular architecture research tool: Identification of signaling domains
1998 Standout
PanR1, a Dominant Negative Missense Allele of the Gene Encoding TNF-α (Tnf), Does Not Impair Lymphoid Development
2006 StandoutNobel
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
Protein folding pathology in domestic animals
2004
Autophagy in Health and Disease: A Double-Edged Sword
2004 StandoutScience
Works of Eran Pras being referenced
Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome
2008
Refined Mapping of the CSNU3 Gene to a 1.8-Mb Region on Chromosome 19q13.1 Using Historical Recombinants in Libyan Jewish Cystinuria Patients
1999
Pacemaker Endocarditis Report of 44 Cases and Review of the Literature
1994
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
2017
Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts
2011
Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).
1996
A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family
2002
Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.
1996
Clinical differences between North African and Iraqi Jews with familial Mediterranean fever
1998
Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.
1993
Genotype-phenotype assessment of common genotypes among patients with familial Mediterranean fever.
2000
Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features.
1997
A Nonsense Mutation in the Glucosaminyl (N-acetyl) Transferase 2 Gene (GCNT2): Association with Autosomal Recessive Congenital Cataracts
2004
A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family.
2000