Malcolm A. Ferguson-Smith

1.7k citations

14 papers · 1.3k indexed · h-index 13

Impact in

Cancer Research top 5%
- Cancer, Hypoxia, and Metabolism
Genetics top 5%
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Genetic and Kidney Cyst Diseases 1
Molecular Biology 10
- Epigenetics and DNA Methylation 2
- Advanced biosensing and bioanalysis techniques 1
- Genomics and Phylogenetic Studies 1
- Hedgehog Signaling Pathway Studies 1

Co-authors: Keith Foster Paul A. Crossey Eamonn R. Maher Amanda Prowse B. Zbar Michael I. Lerman Nabeel A. Affara Frances M. Richards
Journals: Human Molecular Genetics (5 papers)Chromosome Research (3 papers)Nature Genetics (2 papers)Genomics (2 papers)Human Genetics (1 paper)
Partner nations: United Kingdom United States Canada

In The Last Decade

Malcolm A. Ferguson-Smith

14 papers receiving 1.3k citations

Peers

Countries citing papers authored by Malcolm A. Ferguson-Smith

Since Specialization

Citations

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

Fields of papers citing papers by Malcolm A. Ferguson-Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Malcolm A. Ferguson-Smith. 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 Malcolm A. Ferguson-Smith. The network helps show where Malcolm A. Ferguson-Smith may publish in the future.

Co-authors

The 25 scholars most cited alongside Malcolm A. Ferguson-Smith, 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 Malcolm A. Ferguson-Smith Line = papers co-authored together Malcolm A. Ferguson-Smith links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work
1	Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes American Journal of Medical Genetics ·Deepak Kamnasaran, Patricia C. O’Brien, Simone Schuffenhauer, Oliver Quarrell, James R. Lupski, Paola Grammatico, Malcolm A. Ferguson-Smith, D.W. Cox	2001	29
2	Reciprocal chromosome painting illuminates the history of genome evolution of the domestic cat, dog and human Chromosome Research ·Fengtang Yang, Alexander S. Graphodatsky, Patrícia C. M. O’Brien, Amanda Colabella, Nita Solanky, Michael Squire, David R. Sargan, Malcolm A. Ferguson-Smith	2000	91
3	A novel source of highly specific chromosome painting probes for human karyotype analysis derived from primate homologues Human Genetics ·Stefan Müller, Patricia C. O’Brien, Malcolm A. Ferguson-Smith, Johannes Wienberg	1997	26
4	A fast, novel approach for DNA fibre-fluorescence in situ hybridization analysis Chromosome Research ·Suzanne M. Mann, Dean J. Burkin, Darren K. Griffin, Malcolm A. Ferguson-Smith	1997	16
5	Isolation of chromosome-specific paints from high-resolution flow karyotypes of the sheep (Ovis aries) Chromosome Research ·Dean J. Burkin, Patricia C. O’Brien, T. E. Broad, Diana F. Hill, Carol Jones, Johannes Wienberg, Malcolm A. Ferguson-Smith	1997	25
6	Multicolour spectral karyotyping of mouse chromosomes Nature Genetics ·Marek Liyanage, Allen Coleman, Stanislas du Manoir, Tim Veldman, Stephen J. McCormack, Robert B. Dickson, Carrolee Barlow, Anthony Wynshaw‐Boris, Siegfried Janz, Johannes Wienberg, Malcolm A. Ferguson-Smith, Evelin Schröck, Thomas Ried	1996	243
7	Physical analysis of the tuberous sclerosis region in 9q34 Genomics ·Chun Zhou, Ke Wu, Margaret Leversha, Robert A. Furlong, Malcolm A. Ferguson-Smith, Nabeel A. Affara	1995	7
8	Somatic mutations of the von Hippel — Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma Human Molecular Genetics ·Keith Foster, Amanda Prowse, Anke van den Berg, Stewart Fleming, Miriam Hulsbeek, Paul A. Crossey, Frances M. Richards, Paul Cairns, Nabeel A. Affara, Malcolm A. Ferguson-Smith, Charles H. C. M. Buys, Eamonn R. Maher	1994	307
9	A Multicopy Dinucleotide Marker That Maps Close to the Spinal Muscular Atrophy Gene Genomics ·Arthur H.M. Burghes, Susan E. Ingraham, Michael J. McLean, Terri G. Thompson, John D. McPherson, Zsofia Kote‐Jarai, John D. Carpten, Christine J. DiDonato, Joh-E Ikeda, Linda Surh, Brunhilde Wirth, Carole A. Sargent, Malcolm A. Ferguson-Smith, Paul A. Fuerst, Robert K. Moyzis, Deborah Grady, Klaus Zerres, Robert G. Korneluk, Alex MacKenzie, John J. Wasmuth	1994	45
10	Detailed mapping of germline deletions of the von Hippel—Lindau disease tumour suppressor gene Human Molecular Genetics ·Frances M. Richards, Paul A. Crossey, Maude E. Phlpps, Keith Foster, Farida Latif, D. Gareth Evans, Julian R. Sampson, Michael I. Lerman, B. Zbar, Nabeel A. Affara, Malcolm A. Ferguson-Smith, Eamonn R. Maher	1994	61
11	Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence Nature Genetics ·David C. Rubinsztein, William Amos, Jayne Leggo, Sandy Goodburn, Raj Ramesar, John Old, Ronald E. Bontrop, Robert McMahon, David Barton, Malcolm A. Ferguson-Smith	1994	108
12	Direct, non-radioactive detection of mutations in Multiple Endocrine Neoplasia Type 2A families Human Molecular Genetics ·Robert McMahon, Lois M. Mulligan, Catherine S. Healey, Stewart J. Payne, Margaret A. Ponder, Malcolm A. Ferguson-Smith, David Barton, B A Ponder	1994	35
13	Identification of intragenic mutations in the Von Hippel — Lindau disease tumour suppressor gene andcorrelation with disease phenotype Human Molecular Genetics ·Paul A. Crossey, Frances M.Richards, Keith Foster, Jane S. reen, Amanda Prowse, Farida Latlf, Michael I. Lerman, B. Zbar, Nabeel A. Atfara, Malcolm A. Ferguson-Smith, Eamonn R. Maher	1994	304
14	A molecular deletion map of the Y chromosome long arm defining X and autosomal homologous regions and the localisation of the HYA locus to the proximal region of the Yq euchromatin Human Molecular Genetics ·Amanda O’Reilly, Nabeel A. Affara, Elizabeth Simpson, Phillip Chandler, Els Goulmy, Malcolm A. Ferguson-Smith	1992	23

About Malcolm A. Ferguson-Smith

Malcolm A. Ferguson-Smith is a scholar working on Genetics, Molecular Biology, Cancer Research, Genetics and Oncology, having authored 14 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Epigenetics and DNA Methylation (2 papers), Chromosomal and Genetic Variations (2 papers), Cancer, Hypoxia, and Metabolism (2 papers), Advanced biosensing and bioanalysis techniques (1 paper), Genetic and Kidney Cyst Diseases (1 paper), Genomics and Phylogenetic Studies (1 paper) and Hedgehog Signaling Pathway Studies (1 paper). The work is most often cited by research in Cancer Research (513 citations), Genetics (373 citations), Molecular Biology (884 citations), Genetics (88 citations) and Oncology (201 citations). Malcolm A. Ferguson-Smith has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Keith Foster, Paul A. Crossey, Eamonn R. Maher, Amanda Prowse, B. Zbar, Michael I. Lerman, Nabeel A. Affara, Frances M. Richards, Johannes Wienberg and Anke van den Berg. Their work appears in journals such as Human Molecular Genetics, Chromosome Research, Nature Genetics, Genomics and Human 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.

Explore authors with similar magnitude of impact