List of works - Hassan Rokni-Zadeh

A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia

scientific article published on 30 September 2019

Assessing the impact of exact reads on reducing the error rate of read mapping

scientific article published on 06 November 2018

Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation

scientific article published on 22 February 2019

Co-expressional conservation in virulence and stress related genes of three Gammaproteobacterial species: Escherichia coli, Salmonella enterica and Pseudomonas aeruginosa.

scientific article published on 21 September 2015

Distinct lipopeptide production systems for WLIP (white line-inducing principle) in Pseudomonas fluorescens and Pseudomonas putida

scientific article published on 4 December 2012

Draft Genome Sequence of Cyclic Lipopeptide Producer Pseudomonas sp. Strain SWRI103, Isolated from Wheat Rhizosphere

scientific article published on 02 July 2020

Draft Genome Sequence of Kocuria rhizophila RF, a Radiation-Resistant Soil Isolate

scientific article

Draft Genome Sequence of Pseudomonas aeruginosa Strain LMG 1272, an Atypical White Line Reaction Producer

scientific article published on 13 February 2020

Draft Genome Sequence of Pseudomonas fluorescens LMG 5329, a White Line-Inducing Principle-Producing Bioindicator for the Mushroom Pathogen Pseudomonas tolaasii

scientific article published on 25 July 2013

Draft Genome Sequence of Pseudomonas gingeri Strain LMG 5327, the Causative Agent of Ginger Blotch in Agaricus bisporus.

scientific article

Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia

scientific article published on 10 October 2017

GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenita

scientific article published on 22 May 2019

Genetic and functional characterization of cyclic lipopeptide white-line-inducing principle (WLIP) production by rice rhizosphere isolate Pseudomonas putida RW10S2.

scientific article published on 27 April 2012

Impact of a stereocentre inversion in cyclic lipodepsipeptides from the viscosin group: a comparative study of the viscosinamide and pseudodesmin conformation and self-assembly ⬇️

scientific article published on 7 November 2014

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

scientific article published on 03 July 2019

Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report

scientific article published on 26 September 2018

Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature.

scientific article published on 19 October 2016

PCR detection of novel non-ribosomal peptide synthetase genes in lipopeptide-producing Pseudomonas.

scientific article published on 7 June 2011

The antimicrobial compound xantholysin defines a new group of Pseudomonas cyclic lipopeptides ⬇️

scientific article

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

scientific article published on 29 February 2024

Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss

scientific article published on 08 September 2018

List of works by Hassan Rokni-Zadeh

A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia

Assessing the impact of exact reads on reducing the error rate of read mapping

Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation

Co-expressional conservation in virulence and stress related genes of three Gammaproteobacterial species: Escherichia coli, Salmonella enterica and Pseudomonas aeruginosa.

Distinct lipopeptide production systems for WLIP (white line-inducing principle) in Pseudomonas fluorescens and Pseudomonas putida

Draft Genome Sequence of Cyclic Lipopeptide Producer Pseudomonas sp. Strain SWRI103, Isolated from Wheat Rhizosphere

Draft Genome Sequence of Kocuria rhizophila RF, a Radiation-Resistant Soil Isolate

Draft Genome Sequence of Pseudomonas aeruginosa Strain LMG 1272, an Atypical White Line Reaction Producer

Draft Genome Sequence of Pseudomonas fluorescens LMG 5329, a White Line-Inducing Principle-Producing Bioindicator for the Mushroom Pathogen Pseudomonas tolaasii

Draft Genome Sequence of Pseudomonas gingeri Strain LMG 5327, the Causative Agent of Ginger Blotch in Agaricus bisporus.

Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia

GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenita

Genetic and functional characterization of cyclic lipopeptide white-line-inducing principle (WLIP) production by rice rhizosphere isolate Pseudomonas putida RW10S2.

Impact of a stereocentre inversion in cyclic lipodepsipeptides from the viscosin group: a comparative study of the viscosinamide and pseudodesmin conformation and self-assembly ⬇️

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report

Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature.

PCR detection of novel non-ribosomal peptide synthetase genes in lipopeptide-producing Pseudomonas.

The antimicrobial compound xantholysin defines a new group of Pseudomonas cyclic lipopeptides ⬇️

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss