Jennie Slee

1.7k total citations
20 papers, 731 citations indexed

About

Jennie Slee is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Jennie Slee has authored 20 papers receiving a total of 731 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Surgery. Recurrent topics in Jennie Slee's work include Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (2 papers). Jennie Slee is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (2 papers). Jennie Slee collaborates with scholars based in Australia, Germany and Chile. Jennie Slee's co-authors include Linda Watson, Eve Blair, Nadia Badawi, Eric Haan, Denis Viljoen, Beverly Petterson, Fiona Stanley, Jack Goldblatt, Sarah McIntyre and Meredith Wilson and has published in prestigious journals such as Journal of Autism and Developmental Disorders, Developmental Medicine & Child Neurology and Journal of Medical Genetics.

In The Last Decade

Jennie Slee

18 papers receiving 695 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jennie Slee Australia 12 310 293 202 154 133 20 731
Holly Lea Cintas United States 8 183 0.6× 127 0.4× 207 1.0× 67 0.4× 98 0.7× 9 538
Jessica Sun United States 16 206 0.7× 228 0.8× 81 0.4× 116 0.8× 39 0.3× 32 734
Robin E. Osborn United States 16 151 0.5× 128 0.4× 78 0.4× 168 1.1× 111 0.8× 32 731
A M O'Gorman Canada 14 102 0.3× 271 0.9× 59 0.3× 102 0.7× 28 0.2× 21 753
Janette M. Caulton United Kingdom 5 313 1.0× 122 0.4× 51 0.3× 138 0.9× 74 0.6× 7 647
Andrea Mori Switzerland 17 152 0.5× 284 1.0× 66 0.3× 136 0.9× 21 0.2× 38 962
Israel Alfonso United States 15 154 0.5× 137 0.5× 67 0.3× 231 1.5× 24 0.2× 65 630
O.F. Brouwer Netherlands 15 257 0.8× 229 0.8× 100 0.5× 35 0.2× 21 0.2× 35 541
Emile A. M. Beuls Netherlands 19 82 0.3× 145 0.5× 88 0.4× 382 2.5× 54 0.4× 50 933
Dale M. Swift United States 19 242 0.8× 184 0.6× 96 0.5× 303 2.0× 30 0.2× 45 1.1k

Countries citing papers authored by Jennie Slee

Since Specialization
Citations

This map shows the geographic impact of Jennie Slee's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jennie Slee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jennie Slee more than expected).

Fields of papers citing papers by Jennie Slee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennie Slee. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jennie Slee. The network helps show where Jennie Slee may publish in the future.

Co-authorship network of co-authors of Jennie Slee

This figure shows the co-authorship network connecting the top 25 collaborators of Jennie Slee. A scholar is included among the top collaborators of Jennie Slee based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jennie Slee. Jennie Slee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Arpone, Marta, Lesley Bretherton, David J. Amor, et al.. (2022). Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders. Research in Developmental Disabilities. 131. 104338–104338. 2 indexed citations
2.
Baker, Emma K., S. K. Arora, David J. Amor, et al.. (2021). The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia. Journal of Autism and Developmental Disorders. 53(4). 1682–1692. 6 indexed citations
3.
Baker, Emma K., Merlin G. Butler, Ling Ling, et al.. (2020). Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders. Translational Psychiatry. 10(1). 362–362. 11 indexed citations
4.
Corbett, Mark, Clare L. van Eyk, Dani L. Webber, et al.. (2018). Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy. npj Genomic Medicine. 3(1). 33–33. 27 indexed citations
5.
Carroll, Renée, Raman Kumar, Marie Shaw, et al.. (2017). Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restriction. European Journal of Human Genetics. 25(9). 1078–1082. 6 indexed citations
6.
Baynam, Gareth, Nicholas Pachter, F. Ellis McKenzie, et al.. (2015). AB002. The rare and undiagnosed diseases diagnostic service. Annals of Translational Medicine. 4(2). 3–3.
7.
Smithers‐Sheedy, Hayley, Nadia Badawi, Eve Blair, et al.. (2013). What constitutes cerebral palsy in the twenty‐first century?. Developmental Medicine & Child Neurology. 56(4). 323–328. 157 indexed citations
8.
Tropea, Joanne, et al.. (2008). Use of antipsychotic medications for the management of delirium: an audit of current practice in the acute care setting. International Psychogeriatrics. 21(1). 172–179. 27 indexed citations
9.
Robinson, Wendy P., Jennie Slee, Nicholas M. Smith, et al.. (2007). Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5. American Journal of Medical Genetics Part A. 143A(15). 1752–1759. 30 indexed citations
10.
Kelberman, Daniel, Jess Tyson, David Chandler, et al.. (2001). Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. Human Genetics. 109(6). 638–645. 92 indexed citations
11.
Slee, Jennie, John W. Nelson, Jan E. Dickinson, Peter A Kendall, & Anne Halbert. (2000). Yellow nail syndrome presenting as non-immune hydrops: Second case report. American Journal of Medical Genetics. 93(1). 1–4. 20 indexed citations
12.
Slee, Jennie, John W. Nelson, Jan E. Dickinson, Peter A Kendall, & Anne Halbert. (2000). Yellow nail syndrome presenting as non‐immune hydrops: Second case report. American Journal of Medical Genetics. 93(1). 1–4. 3 indexed citations
13.
Slee, Jennie, Geoffrey C. Lam, & Ian Walpole. (1999). Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification. American Journal of Medical Genetics. 84(4). 330–333.
14.
Slee, Jennie, Geoffrey C. Lam, & Ian Walpole. (1999). Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification. American Journal of Medical Genetics. 84(4). 330–333. 11 indexed citations
15.
Badawi, Nadia, Linda Watson, Beverly Petterson, et al.. (1998). What constitutes cerebral palsy?. Developmental Medicine & Child Neurology. 40(8). 520–527. 196 indexed citations
16.
Slee, Jennie, et al.. (1997). A syndrome of leukonychia totalis and multiple sebaceous cysts. Clinical Dysmorphology. 6(3). 229–231. 8 indexed citations
17.
Slee, Jennie & Jack Goldblatt. (1997). Further evidence for preaxial hallucal polydactyly as a marker of diabetic embryopathy.. Journal of Medical Genetics. 34(3). 261–263. 10 indexed citations
18.
Slee, Jennie & Jack Goldblatt. (1996). Further evidence for a syndrome of “apple peel” intestinal atresia, ocular anomalies and microcephaly. Clinical Genetics. 50(4). 260–262. 13 indexed citations
19.
Singer, Steven L., Eric Haan, Jennie Slee, & Jack Goldblatt. (1994). Familial hemifacial microsomia due to autosomal dominant inheritance. Case reports. Australian Dental Journal. 39(5). 287–291. 20 indexed citations
20.
Slee, Jennie, et al.. (1991). Deletion of chromosome 13 in Moebius syndrome.. Journal of Medical Genetics. 28(6). 413–414. 92 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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