Citation Impact
Citing Papers
Human Hypertension Caused by Mutations in WNK Kinases
2001 StandoutScience
Disturbed Homeostasis in Sodium-Restricted Mice Heterozygous and Homozygous for Aldosterone Synthase Gene Disruption
2006 StandoutNobel
Case Detection, Diagnosis, and Treatment of Patients with Primary Aldosteronism: An Endocrine Society Clinical Practice Guideline
2008 Standout
Rodent-borne diseases and their risks for public health
2009 Standout
Guideline for disinfection and sterilization in healthcare facilities, 2008
2008 Standout
Management Guidelines for Children with Thyroid Nodules and Differentiated Thyroid Cancer
2015 Standout
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel
1995
ECLAMC: The Latin-American Collaborative Study of Congenital Malformations
2004 Standout
A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in North African Jews with phenylketonuria
1993
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
Antibiotic policies for short-term catheter bladder drainage in adults
2005
Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents
2017 Standout
Antioxidative peptides from food proteins: A review
2010 Standout
Cockayne syndrome: Review of 140 cases
1992
Clinical, Clinicopathologic, and Hematologic Features of Kyasanur Forest Disease
1989
World distribution of factor V Leiden
1995 Standout
Prevalence of intellectual disability: A meta-analysis of population-based studies
2011 Standout
Kidney function in mice lacking aldosterone
2005 StandoutNobel
Why are some genetic diseases common?
1993
Hypertension in patients with cushing’s disease: Pathophysiology, diagnosis, and management
2005
Psychosocial resilience and protective mechanisms.
1987 Standout
Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis
2003 Standout
The Hutchinson-Gilford progeria syndrome
1972
Geometric and Electronic Structure/Function Correlations in Non-Heme Iron Enzymes
1999 Standout
Epidemiology of congenital pigmented naevi:.
1981
INTESTINAL ASSIMILATION OF INTACT PEPTIDES AND PROTEINS FROM THE DIET‐A NEGLECTED FIELD?
1984
Clinical practice guidelines for antimicrobial prophylaxis in surgery
2013 Standout
Risk factors for mental retardation.
1985
Disorders of Glutamate Metabolism and Neurological Dysfunction
1981 StandoutNobel
The Significance of Elevated Levels of Plasma 18-Hydroxycorticosterone in Patients with Primary Aldosteronism*
1979
ICRP PUBLICATION 118: ICRP Statement on Tissue Reactions and Early and Late Effects of Radiation in Normal Tissues and Organs — Threshold Doses for Tissue Reactions in a Radiation Protection Context
2012 Standout
Inborn Error in the Terminal Step of Aldosterone Biosynthesis
1980
The alleged antecedent brother effect in sex ratio
1985
Yeast Nucleotide Excision Repair Proteins Rad2 and Rad4 Interact with RNA Polymerase II Basal Transcription Factor b (TFIIH)
1994 StandoutNobel
Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): Role of increased renal chloride reabsorption
1981
Yeast nucleotide excision repair proteins Rad2 and Rad4 interact with RNA polymerase II basal transcription factor b (TFIIH).
1994 StandoutNobel
Diagnosis, Prevention, and Treatment of Catheter-Associated Urinary Tract Infection in Adults: 2009 International Clinical Practice Guidelines from the Infectious Diseases Society of America
2010 Standout
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
Maternal Phenylketonuria and Hyperphenylalaninemia
1980
The human sex ratio. Part 1: A review of the literature.
1987 Standout
The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline
2016 Standout
An immunoreactive theory of selective male affliction
1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiency.
1985 Standout
Ureteropelvic Junction Obstruction
2012
The Natural History of Salt-Wasting Disorders of Adrenal and Renal Origin*
1984
IS PROPHYLACTIC ANTIMICROBIAL TREATMENT NECESSARY AFTER HYPOSPADIAS REPAIR?
2004
Cockayne syndrome group B protein enhances elongation by RNA polymerase II
1997 StandoutNobel
Resistant Hypertension: Diagnosis, Evaluation, and Treatment
2008 Standout
Works of B. E. Cohen being referenced
Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria.
1991
Symptomatic spinal epidural lipomatosis in a patient with Cushing's disease
1995
A single origin of phenylketonuria in Yemenite Jews
1990 Nature
Postoperative catheterization and prophylactic antimicrobials in children with hypospadias
1983
Amino-aciduria and Hypermetabolism in Progeria
1957
Cysteine peptiduria in a mentally retarded patient
1973
Ureteropelvic Junction Obstruction: Its Occurrence in 3 Members of a Single Family
1978
Relative importance of genetic and nongenetic etiologies in idiopathic mental retardation: estimates based on analysis of medical histories
1983
Pathogenic Factors in Idiopathic Mental Retardation
1981
Phenylketonuria (PKU) in Israel
2015
IgE induces secretion of prostaglandin E2 by human monocytes.
1984
MENTAL RETARDATION IN A FAMILY WITH PHENYLKETONURIA AND MILD HYPERPH ENYLALANINEMIA
1969
BIOLOGICAL FACTORS IN MILD MENTAL RETARDATION
1983
Metabolic Responses to the Administration of Angiotensin II, K and ACTH in Two Salt-Wasting Syndromes
1977
Collagen synthesis by fibroblasts in a patient with the Cockayne syndrome
1981
GENETIC CONSIDERATIONS IN GIANT PIGMENTED HAIRY NAEVUS
1971