Concepedia

Author

David Francis

Victorian Clinical Genetics ServicesORCID

Also Known As

D Francis, D. Francis, D., Francis, D.I. Francis, DAVID FRANCIS, David Francis, David I Francis, David I. Francis, Francis, David

95

Publications

2.5K

Citations

27

H-Index

90

Concepts

All Affiliations

Victorian Clinical Genetics ServicesMurdoch Children's Research InstituteRoyal Children's HospitalThe University of MelbourneLa Trobe University
DF

About

David Francis is an author at Victorian Clinical Genetics Services specializing in medicine, genetics, and public health.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

16

16

1.1K

2

Public Health

7

7

252

3

Health Sciences

2

2

208

4

Engineering

1

1

157

5

Natural Sciences

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29

David Francis

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51

Publications

2.4K

Citations

26

H-Index

YearCitations

A Genetic Association Study of the Functional A118G Polymorphism of the Human ??-Opioid Receptor Gene in Patients with Acute and Chronic Pain

Piotr K. Janicki, Gregg H. Schuler, David Francis,

Anesthesia & Analgesia

2006

166

ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism

Radha Desai, Ann E. Frazier, Romina Durigon,

Brain

2017

157

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

Przemysław Szafrański, Tomasz Gambin, Avinash V. Dharmadhikari,

Human Genetics

2016

155

NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits

Piotr Dittwald, Tomasz Gambin, Przemysław Szafrański,

Genome Research

2013

143

Integrated multi-omics for rapid rare disease diagnosis on a national scale

Sebastian Lunke, Sophie E. Bouffler, Chirag Patel,

Nature Medicine

2023

122

Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests

Alison D. Archibald, Melanie Smith, Trent Burgess,

Genetics in Medicine

2017

117

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

Ricky S. Joshi, Paras Garg, Noah Zaitlen,

The American Journal of Human Genetics

2016

115

Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping

Damien L. Bruno, Stuart White, Devika Ganesamoorthy,

Journal of Medical Genetics

2011

105

Pallister–Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p

Alison Yeung, David Francis, Olivia Giouzeppos,

American Journal of Medical Genetics Part A

2009

86

Two cases of trisomy 16 mosaicism ascertained postnatally

Claudine Rieubland, David Francis, Leonie Houben,

American Journal of Medical Genetics Part A

2009

84

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