Ross Brookwell

792 citations

14 papers · 421 indexed · h-index 9

Impact in

Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Cognitive Neuroscience
- Autism Spectrum Disorder Research

Papers in ⓘ

Genetics 9
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetic Syndromes and Imprinting 2
- Genomic variations and chromosomal abnormalities 2
- Myeloproliferative Neoplasms: Diagnosis and Treatment 1
Molecular Biology 5
- Advanced biosensing and bioanalysis techniques 1

Co-authors: Gillian Turner (5 shared papers)Art Daniel (5 shared papers)Mark Selikowitz (2 shared papers)John M. Opitz (2 shared papers)Patricia A. Jacobs (1 shared paper)Stuart Purvis‐Smith (1 shared paper)Lesley Stewart (1 shared paper)Lillian Y. F. Hsu (1 shared paper)
Journals: Obstetrical & Gynecological Survey (1 paper)BioMed Research International (1 paper)Histopathology (1 paper)New England Journal of Medicine (1 paper)Clinical Genetics (1 paper)
Partner nations: Australia Sweden Germany

In The Last Decade

Ross Brookwell

14 papers receiving 381 citations

Peers

Countries citing papers authored by Ross Brookwell

Since Specialization

Citations

This map shows the geographic impact of Ross Brookwell'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 Ross Brookwell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ross Brookwell more than expected).

Fields of papers citing papers by Ross Brookwell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ross Brookwell. 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 Ross Brookwell. The network helps show where Ross Brookwell may publish in the future.

Co-authors

The 25 scholars most cited alongside Ross Brookwell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ross Brookwell Line = papers co-authored together Ross Brookwell links everyone, so they are left out of the graph.

All Works

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14 of 14 papers shown

#	Work
1	Heterozygous Expression of X-Linked Mental Retardation and X-Chromosome Marker Fra(X)(Q27) New England Journal of Medicine ·Gillian Turner, Ross Brookwell, Art Daniel, Mark Selikowitz, Michael Zilibowitz	1980	149
2	The diagnosis and frequency of X‐linked conditions in a cohort of moderately retarded males with affected brothers American Journal of Medical Genetics ·Jane Fishburn, Gillian Turner, Art Daniel, Ross Brookwell, John M. Opitz	1983	90
3	The fragile X(q27) form of X‐linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes American Journal of Medical Genetics ·Ross Brookwell, Art Daniel, Gillian Turner, Jane Fishburn, John M. Opitz	1982	45
4	Prenatal diagnosis in 3,000 women for chromosome, X‐linked, and metabolic disorders American Journal of Medical Genetics ·Art Daniel, Lesley Stewart, Toni Saville, Ross Brookwell, Helen Paull, Stuart Purvis‐Smith, P.R.L.C. Lam-Po-Tang, Patricia A. Jacobs, Lillian Y. F. Hsu	1982	32
5	Proximal 15q variant with normal phenotype in three unrelated individuals Clinical Genetics ·Ross Brookwell, Adam Veleba	1987	24
6	High resolution banding and the locus of the Xq fragile site Human Genetics ·Ross Brookwell, Gillian Turner	1983	23
7	FISH Detection ofPML-RARAFusion in ins(15;17) Acute Promyelocytic Leukaemia Depends on Probe Size BioMed Research International ·Lynda J. Campbell, Paul Oei, Ross Brookwell, Jake Shortt, Nicola Eaddy, Ashley P. Ng, Edward Chew, Peter Browett	2013	20
8	Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution Genes Chromosomes and Cancer ·Bin Tean Teh, Elizabeth Blennow, Sophie Giraud S, Sigrid Sahlén, Su I. Hii, Ross Brookwell, Hiltrud Brauch, Magnus Nordenskjöld, Catharina Larsson, David Nicol	1998	17
9	Formation of double minutes by breakdown of a homogeneously staining region in a refractory anemia with excess blasts Cancer Genetics and Cytogenetics ·Ross Brookwell, Frederick A. Hunt	1988	8
10	Lessons learnt from MDM2 fluorescence in‐situ hybridisation analysis of 439 mature lipomatous lesions with an emphasis on atypical lipomatous tumour/well‐differentiated liposarcoma lacking cytological atypia Histopathology ·Ana Cristina Vargas, Christopher Joy, Alison L. Cheah, Martin Jones, Fiona Bonar, Ross Brookwell, Bernadette Garrone, Joel Talbot, James Harraway, Anthony J. Gill, Fiona Maclean	2021	5
11	A comparative analysis of the karyotypes of three dolphins – Tursiops truncatus Montagu, 1821, Tursiops australis Charlton-Robb et al., 2011, and Grampus griseus Cuvier, 1812 Comparative Cytogenetics ·Ross Brookwell, Kimberly A. Finlayson, Jason P. van de Merwe	2021	3
12	A “Double-Hit” Translocation Sarcoma—First Report of the Co-occurrence of EWSR1-FLI1 and MTMR2-NTRK2 Fusion in a Small Round Blue Cell Sarcoma Ana Cristina Vargas, Caroline Kurek, Fiona Bonar, Fiona Maclean, Min Qiu, Richard Boyle, Ross Brookwell, Anthony J. Gill	2020	2
13	Heterozygous Expression of X-Linked Mental Retardation and X-Chromosome Marker fra(X)(q27) Obstetrical & Gynecological Survey ·Gillian Turner, Ross Brookwell, Art Daniel, Mark Selikowitz, MICHAEL ZILBOWITZ	1981	2
14	A case report of an ETV6-ABL1 [t(6;9;12)] positive myeloproliferative neoplasm Pathology ·Tennille Pelly, Yasmin Harvey, Ross Brookwell, Helen Wordsworth, Tee Beng Keng	2013	1

About Ross Brookwell

Ross Brookwell is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Rheumatology and Hematology, having authored 14 papers that have together received 421 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genetic Syndromes and Imprinting (2 papers), Sarcoma Diagnosis and Treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Advanced biosensing and bioanalysis techniques (1 paper), Soft tissue tumor case studies (1 paper) and Myeloproliferative Neoplasms: Diagnosis and Treatment (1 paper). The work is most often cited by research in Genetics (326 citations), Cognitive Neuroscience (79 citations), Speech and Hearing (27 citations), Pediatrics, Perinatology and Child Health (64 citations) and Molecular Biology (191 citations). Ross Brookwell has collaborated with scholars based in Australia, Sweden and Germany. Frequent co-authors include Gillian Turner, Art Daniel, Mark Selikowitz, John M. Opitz, Patricia A. Jacobs, Stuart Purvis‐Smith, Lesley Stewart, Lillian Y. F. Hsu, P.R.L.C. Lam-Po-Tang and Paul Oei. Their work appears in journals such as Obstetrical & Gynecological Survey, BioMed Research International, Histopathology, New England Journal of Medicine and Clinical Genetics.

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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