Concepedia

Author

Jennie Slee

Princess Margaret Hospital for Children

Also Known As

J J SLEE, J J Slee, J Slee, J. Slee, Jennie Slee, Slee, J

35

Publications

1.7K

Citations

18

H-Index

21

Concepts

All Affiliations

Princess Margaret Hospital for ChildrenKing Edward Memorial HospitalThe University of Western AustraliaWomen's and Children's HospitalQueen Elizabeth II Medical Centre
JS

About

Jennie Slee is an author at Princess Margaret Hospital for Children specializing in medicine, genetics, and developmental biology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

553

2

Public Health

1

1

276

3

Diabetes

1

1

13

4

Molecular Genetics

1

1

276

5

Obstetrics

1

1

13

Jennie Slee

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18

Publications

1.2K

Citations

15

H-Index

YearCitations

Identification of SOX3 as an XX male sex reversal gene in mice and humans

Edwina Sutton, James Hughes, Stefan J. White,

Journal of Clinical Investigation

2010

276

Deletion of chromosome 13 in Moebius syndrome.

Jennie Slee, R. D. Smart, Denis Viljoen

Journal of Medical Genetics

1991

133

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

Daniel Kelberman, Jess Tyson, David Chandler,

Human Genetics

2001

131

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Emily J. Todd, Kyle S. Yau, Royston Ong,

Orphanet Journal of Rare Diseases

2015

113

Haploinsufficiency of SF3B2 causes craniofacial microsomia

Andrew T. Timberlake, Casey Griffin, Carrie L. Heike,

Nature Communications

2021

86

The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service

Gareth Baynam, Nicholas Pachter, F. Ellis McKenzie,

Orphanet Journal of Rare Diseases

2016

73

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

Alicia B. Byrne, Peer Arts, Thuong Ha,

Nature Medicine

2023

54

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy

Mark Corbett, Clare L. van Eyk, Dani L. Webber,

npj Genomic Medicine

2018

47

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5

Wendy P. Robinson, Jennie Slee, Nicholas M. Smith,

American Journal of Medical Genetics Part A

2007

42

Initiating an undiagnosed diseases program in the Western Australian public health system

Gareth Baynam, Stephanie Broley, Alicia Bauskis,

Orphanet Journal of Rare Diseases

2017

40

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