List of works - Zornitza Stark

A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data.

scientific article

A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations.

scientific article published on 7 December 2017

A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis

scientific article published on 18 July 2019

A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

scientific article

A novel presentation of homozygous loss-of-function STAT-1 mutation in an infant with hyperinflammation-A case report and review of the literature

scientific article published on 22 April 2016

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

scientific article published on 3 March 2016

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.

scientific article published in December 2017

ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome

scientific article published on 2 March 2017

Apert syndrome: temporal lobe abnormalities on fetal brain imaging.

scientific article

Association of severe autosomal recessive osteopetrosis and structural brain abnormalities: A case report and review of the literature ⬇️

scientific article published on October 17, 2012

Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function

scientific article published on 17 January 2022

Clinical problem-solving. Spot diagnosis

scientific article

Cpipe: a shared variant detection pipeline designed for diagnostic settings

scientific article published on 10 July 2015

Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions.

scientific article published on 21 January 2013

De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations

scientific article published on 27 January 2016

De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic features

scientific article published on 27 July 2010

De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy

scientific article published on 24 June 2016

De novo mutations in HNRNPU result in a neurodevelopmental syndrome

scientific article published on 25 September 2017

Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1

scientific journal article

Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.

scientific article

Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy.

scientific article

Discussing withholding and withdrawing of life-sustaining medical treatment in paediatric inpatients: audit of current practice

scientific article published on July 2008

Ethical controversies in prenatal microarray

scientific article published on April 2013

Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders.

scientific article published on 16 February 2018

Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins

scientific article published on 12 November 2017

Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays

scientific article published on 19 September 2011

Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases

scientific article published on 14 October 2015

GA4GH: International policies and standards for data sharing across genomic research and healthcare

scientific article published on 10 November 2021

Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates

article

Genotype and phenotype spectrum of NRAS germline variants

scientific article published on 3 May 2017

Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome

scientific article

Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutations

scientific article

Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring

scientific article

KBG syndrome: An Australian experience

scientific article

Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomes

scientific article published on 21 May 2019

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

scientific article

MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability

scientific article published on 19 June 2017

Meeting report of the 2017 KidGen Renal Genetics Symposium

scientific article published on 30 January 2018

Metronidazole Toxicity in Cockayne Syndrome: A Case Series.

scientific article published on 24 August 2015

Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

scientific article published on 26 March 2013

Multi-omic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10

scientific article published on 10 November 2020

Mutations in CSPP1 Cause Primary Cilia Abnormalities and Joubert Syndrome with or without Jeune Asphyxiating Thoracic Dystrophy

Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy

scientific article

Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome

scientific article

Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study

scientific article published on 6 February 2018

Osteopetrosis

Phenotypic variability of distal 22q11.2 copy number abnormalities

article

Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway

Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?

scientific article published on 8 June 2016

Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement.

scientific article published on 26 January 2017

Rapid Genomic Testing in Intensive Care: Health Professionals’ Perspectives on Ethical Challenges

scientific article published in 2023

Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate

scientific article published on 09 September 2020

Renal Genetics in Australia: Kidney Medicine in the Genomic Age

article

SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia

scientific article published on 8 June 2015

The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care.

scientific article published on 23 July 2015

The SMAD-binding domain of SKI: a hotspot for de novo mutations causing Shprintzen-Goldberg syndrome

scientific article

The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy

scientific article published on 22 May 2020

Triad of tracheoesophageal fistula-esophageal atresia, pulmonary hypoplasia, and duodenal atresia

scientific article published on June 2007

List of works by Zornitza Stark

A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data.

A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations.

A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis

A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

A novel presentation of homozygous loss-of-function STAT-1 mutation in an infant with hyperinflammation-A case report and review of the literature

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.

ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome

Apert syndrome: temporal lobe abnormalities on fetal brain imaging.

Association of severe autosomal recessive osteopetrosis and structural brain abnormalities: A case report and review of the literature ⬇️

Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function

Clinical problem-solving. Spot diagnosis

Cpipe: a shared variant detection pipeline designed for diagnostic settings

Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions.

De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations

De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic features

De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy

De novo mutations in HNRNPU result in a neurodevelopmental syndrome

Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1

Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.

Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy.

Discussing withholding and withdrawing of life-sustaining medical treatment in paediatric inpatients: audit of current practice

Ethical controversies in prenatal microarray

Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders.

Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins

Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays

Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases

GA4GH: International policies and standards for data sharing across genomic research and healthcare

Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates

Genotype and phenotype spectrum of NRAS germline variants

Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome

Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutations

Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring

KBG syndrome: An Australian experience

Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomes

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability

Meeting report of the 2017 KidGen Renal Genetics Symposium

Metronidazole Toxicity in Cockayne Syndrome: A Case Series.

Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

Multi-omic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10

Mutations in CSPP1 Cause Primary Cilia Abnormalities and Joubert Syndrome with or without Jeune Asphyxiating Thoracic Dystrophy

Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy

Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome

Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study

Osteopetrosis

Phenotypic variability of distal 22q11.2 copy number abnormalities

Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway

Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?

Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement.

Rapid Genomic Testing in Intensive Care: Health Professionals’ Perspectives on Ethical Challenges

Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate

Renal Genetics in Australia: Kidney Medicine in the Genomic Age

SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia

The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care.

The SMAD-binding domain of SKI: a hotspot for de novo mutations causing Shprintzen-Goldberg syndrome

The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy

Triad of tracheoesophageal fistula-esophageal atresia, pulmonary hypoplasia, and duodenal atresia