Ruth N. MacKinnon

1.0k citations

31 papers · 739 indexed · h-index 15

Co-authors: Lynda J. Campbell Mark C. Hirst M.V. Bell Yutaka Nakahori Tracey Flint A. Roche Kay E. Davies U. Froster‐Iskenius
Topics: Genomic variations and chromosomal abnormalities (11 papers)Acute Myeloid Leukemia Research (9 papers)Chromosomal and Genetic Variations (7 papers)
Cited by: Genetics Molecular Biology Hematology
Journals: Cell Nucleic Acids Research Scientific Reports
Partner nations: Australia United Kingdom United States

In The Last Decade

Ruth N. MacKinnon

30 papers receiving 725 citations

Peers

Countries citing papers authored by Ruth N. MacKinnon

Since Specialization

Citations

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

Fields of papers citing papers by Ruth N. MacKinnon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruth N. MacKinnon. 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 Ruth N. MacKinnon. The network helps show where Ruth N. MacKinnon may publish in the future.

Co-authorship network of co-authors of Ruth N. MacKinnon

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth N. MacKinnon. A scholar is included among the top collaborators of Ruth N. MacKinnon 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 Ruth N. MacKinnon. Ruth N. MacKinnon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instability 2020 ·Molecular Cytogenetics ·Ruth N. MacKinnon,(unknown),Lynda J. Campbell,Meaghan Wall	0
2	Hemopoietic Cell Kinase amplification with Protein Tyrosine Phosphatase Receptor T depletion leads to polycythemia, aberrant marrow erythoid maturation, and splenomegaly 2019 ·Scientific Reports ·Matthew Ku,Ruth N. MacKinnon,Meaghan Wall,Nisha Narayan,Carl R. Walkley,Heung‐Chin Cheng,Lynda J. Campbell,Louise E. Purton,Harshal Nandurkar	4
3	The Dicentric Chromosome dic(20;22) Is a Recurrent Abnormality in Myelodysplastic Syndromes and Is a Product of Telomere Fusion 2016 ·Cytogenetic and Genome Research ·Ruth N. MacKinnon,Hendrika M. Duivenvoorden,Lynda J. Campbell,Meaghan Wall	2
4	Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement 2013 ·Cancer Genetics ·Ruth N. MacKinnon,Lynda J. Campbell	23
5	Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL 2013 ·Evolution Medicine and Public Health ·Ruth N. MacKinnon,Meaghan Wall,(unknown),(unknown),(unknown),(unknown),Lynda J. Campbell	7
6	CGH and SNP array using DNA extracted from fixed cytogenetic preparations and long-term refrigerated bone marrow specimens 2012 ·Molecular Cytogenetics ·Ruth N. MacKinnon,Carly Selan,(unknown),Meaghan Wall,Harshal Nandurkar,Lynda J. Campbell	6
7	A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes 2011 ·Cancer Genetics ·Ruth N. MacKinnon,George Kannourakis,Meaghan Wall,Lynda J. Campbell	22
8	The Use of M-FISH and M-BAND to Define Chromosome Abnormalities 2011 ·Methods in molecular biology ·Ruth N. MacKinnon,Ilse Chudoba	8
9	Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q 2011 ·Cancer Genetics ·Ruth N. MacKinnon,Hendrika M. Duivenvoorden,Lynda J. Campbell	5
10	The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion 2010 ·Genes Chromosomes and Cancer ·Ruth N. MacKinnon,Carly Selan,Meaghan Wall,Elizabeth Baker,Harshal Nandurkar,Lynda J. Campbell	39
11	Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20 2007 ·Cytogenetic and Genome Research ·Ruth N. MacKinnon,Lynda J. Campbell	14
12	A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes 2006 ·Genes Chromosomes and Cancer ·Ruth N. MacKinnon,(unknown),Ilse Chudoba,Lynda J. Campbell	11
13	Recurrent duplication of Xq27∼qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor banding 2005 ·Cancer Genetics and Cytogenetics ·Ruth N. MacKinnon,(unknown),Lynda J. Campbell	2
14	Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1 1994 ·Mammalian Genome ·Helen J. Blair,Mark C. Hirst,Ruth N. MacKinnon,Kay E. Davies,Yvonne Boyd	2
15	Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome 1991 ·Cell ·M.V. Bell,Mark C. Hirst,Yutaka Nakahori,Ruth N. MacKinnon,A. Roche,Tracey Flint,P. A. Jacobs,Niels Tommerup,Lisbeth Tranebjærg,U. Froster‐Iskenius,Bredford Kerr,Gillian Turner,R H Lindenbaum,Robin Winter,(unknown),Stephen N. Thibodeau,Kay E. Davies	287
16	An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15 1991 ·Mammalian Genome ·Philip J. MacKinnon,Barry C. Powell,George E. Rogers,Elizabeth Baker,Ruth N. MacKinnon,V.J. Hyland,David F. Callen,(unknown)	14
17	PCR walking from microdissection clone M54 identifies three exons from the human gene for the neural cell adhesion molecule L1 (CAM-L1) 1991 ·Nucleic Acids Research ·André Rosenthal,Ruth N. MacKinnon,(unknown),C. Jones	20
18	Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site 1991 ·American Journal of Medical Genetics ·Mark C. Hirst,M.V. Bell,Ruth N. MacKinnon,J. E. Vivienne Watson,David F. Callen,Grant Sutherland,Niklas Dahl,Mark Patterson,Charles E. Schwartz,David H. Ledbetter,Susan A. Ledbetter,Kay E. Davies	7
19	A YAC contig across the fragile X site defines the region of fragility 1991 ·Nucleic Acids Research ·Mark C. Hirst,Katrina Rack,Yutaka Nakahori,A. Roche,M.V. Bell,Geraldine Flynn,(unknown),Ruth N. MacKinnon,Michael J. Francis,(unknown),Rakesh Anand,(unknown),Hans Lehrach,David Schlessinger,Michele D’Urso,Veronica J. Buckle,K.E. Davies	35
20	Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1 1990 ·Human Genetics ·V.J. Hyland,Graeme Suthers,Kathryn Friend,Ruth N. MacKinnon,David F. Callen,M.H. Breuning,Tim P. Keith,Valerie A. Brown,(unknown),G.R. Sutherland	23

About Ruth N. MacKinnon

Ruth N. MacKinnon is a scholar working on Hematology, Genetics and Genetics, having authored 31 papers that have together received 739 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Acute Myeloid Leukemia Research (9 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Genetics (449 citations), Molecular Biology (523 citations) and Hematology (82 citations). Ruth N. MacKinnon has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Lynda J. Campbell, Mark C. Hirst, M.V. Bell, Yutaka Nakahori, Tracey Flint, A. Roche, Kay E. Davies, U. Froster‐Iskenius, P. A. Jacobs and Stephen N. Thibodeau. Their work appears in journals such as Cell, Nucleic Acids Research and Scientific Reports.

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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