Michael F. Buckley

3.1k citations

32 papers · 701 indexed · h-index 15

Co-authors: James W. Goding Daniel P. Siewiorek Tony Roscioli William J. McKinstry Kate L. Loveland O. Margaret Garson Hans Scheffer Erik‐Jan Kamsteeg
Topics: Genomics and Rare Diseases (5 papers)Prenatal Screening and Diagnostics (4 papers)Craniofacial Disorders and Treatments (4 papers)
Cited by: Physiology Genetics Software
Journals: Journal of Biological ChemistrySHILAP Revista de lepidopterologíaCirculation Research
Partner nations: Australia United States United Kingdom

In The Last Decade

Michael F. Buckley

30 papers receiving 691 citations

Peers

Countries citing papers authored by Michael F. Buckley

Since Specialization

Citations

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

Fields of papers citing papers by Michael F. Buckley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael F. Buckley. 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 Michael F. Buckley. The network helps show where Michael F. Buckley may publish in the future.

Co-authorship network of co-authors of Michael F. Buckley

This figure shows the co-authorship network connecting the top 25 collaborators of Michael F. Buckley. A scholar is included among the top collaborators of Michael F. Buckley 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 Michael F. Buckley. Michael F. Buckley 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	Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia 2024 ·SHILAP Revista de lepidopterología ·(unknown),Katie A. Ashton,(unknown),K.T. Lee,Omkar L. Patkar,Emma Krzesinski,(unknown),Erin M. Carter,Cathleen Raggio,Andreas Zankl,Anas M. Khanshour,(unknown),Jonathan J. Rios,Carol A. Wise,Ying Zhu,Futao Zhang,Tony Roscioli,Michael F. Buckley,Victoria L. Harvey,Paul A. Dawson	0
2	Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detection 2018 ·Human Mutation ·Mark J. Cowley,Yu‐Chi Liu,Karen Oliver,Gemma L. Carvill,Candace T. Myers,Velimir Gayevskiy,Martin B. Delatycki,Danique R.M. Vlaskamp,Ying Zhu,Heather C. Mefford,Michael F. Buckley,Melanie Bahlo,Ingrid E. Scheffer,Marcel E. Dinger,Tony Roscioli	6
3	Atypical Skin Manifestations in <b><i>FGFR2</i></b>-Related Craniosynostosis Syndromes Broaden the Phenotypic Spectrum 2018 ·Molecular Syndromology ·Shannon LeBlanc,Dávid Dávid,Alison Colley,Michael F. Buckley,Tony Roscioli,Christopher Barnett	1
4	Beyond the panel: preconception screening in consanguineous couples using the TruSight One “clinical exome” 2018 ·Genetics in Medicine ·Edwin P. Kirk,Kristine Barlow‐Stewart,Arthavan Selvanathan,(unknown),Lisa Worgan,Sulekha Rajagopalan,Mark J. Cowley,Velimir Gayevskiy,A.H. Bittles,Leslie Burnett,George Elakis,William Lo,Michael F. Buckley,Alison Colley,Tony Roscioli	16
5	Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy 2017 ·European Journal of Human Genetics ·Lisa Ewans,Michael Field,Ying Zhu,Gillian Turner,Melanie Leffler,Marcel E. Dinger,Mark J. Cowley,Michael F. Buckley,Ingrid E. Scheffer,Matilda R. Jackson,Tony Roscioli,Cheryl Shoubridge	14
6	Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagine 2015 ·Molecular Genetics and Metabolism ·Elizabeth E. Palmer,(unknown),Rani Sachdev,Michael Cardamone,Tejaswi Kandula,Paula Morris,Kerith‐Rae Dias,Tao Jiang,David F. Miller,Ying Zhu,Rebecca Macintosh,Marcel E. Dinger,Mark J. Cowley,Michael F. Buckley,Tony Roscioli,(unknown),Michael S. Kilberg,Edwin P. Kirk	39
7	Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 2012 ·European Journal of Human Genetics ·Erik‐Jan Kamsteeg,Wolfram Kreß,Claudio Catalli,Jens Michael Hertz,Martina Witsch‐Baumgartner,Michael F. Buckley,Baziel G.M. van Engelen,Marianne Schwartz,Hans Scheffer	100
8	Expanding the clinical spectrum of SLC29A3 gene defects 2010 ·European Journal of Medical Genetics ·Ronen Spiegel,(unknown),Michael F. Buckley,Yanick J. Crow,Jill Urquhart,Yoseph Horovitz,Yardena Tenenbaum‐Rakover,William G. Newman,Dian Donnai,Stavit A. Shalev	35
9	Massively parallel sequencing of ataxia genes after array-based enrichment 2010 ·Human Mutation ·Alexander Hoischen,Christian Gilissen,Peer Arts,Nienke Wieskamp,Walter van der Vliet,Sascha Vermeer,Marloes Steehouwer,Petra de Vries,Rowdy Meijer,(unknown),Nine V.A.M. Knoers,Michael F. Buckley,Hans Scheffer,Joris A. Veltman	63
10	Breast cancer risk is not increased in individuals with TWIST1 mutation confirmed Saethre–Chotzen syndrome: An Australian multicenter study 2009 ·Genes Chromosomes and Cancer ·Paul A. James,Bronwyn Culling,(unknown),Mark A. Jenkins,George Elakis,(unknown),(unknown),Meredith Wilson,Peter J. Anderson,Ravi Savarirayan,(unknown),(unknown),Michael F. Buckley,Kathy Tucker,Tony Roscioli	2
11	SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway 2009 ·Human Molecular Genetics ·(unknown),Jamie M. Kramer,Khalid Hussain,Joris H. Robben,Eiko K. de Jong,Arjan Pm de Brouwer,Esther Nibbeling,Erik‐Jan Kamsteeg,Melanie Wong,Julie Prendiville,Chela James,(unknown),(unknown),Hans van Bokhoven,Peter M.T. Deen,Raoul C. M. Hennekam,Robert W. Lindeman,Annette Schenck,Tony Roscioli,Michael F. Buckley	85
12	Pfeiffer syndrome with neonatal death secondary to tracheal obstruction owing to the FGFR2 Glu565Ala mutation 2008 ·Clinical Dysmorphology ·Lucinda Freeman,George Elakis,Geoff Watson,(unknown),Peter J. Taylor,Peter Anderson,Robert Ogle,Michael F. Buckley,Tony Roscioli	5
13	A case of Beare–Stevenson syndrome with a broad spectrum of features and a review of the FGFR2 Y375C mutation phenotype 2006 ·Clinical Dysmorphology ·Julie McGaughran,(unknown),Rachel Susman,Michael F. Buckley,George Elakis,Timothy C. Cox,Tony Roscioli	18
14	Chromosome 2q24.2 is lost in sporadic but not in BRCA1-associated ovarian carcinomas 2006 ·Pathology ·Morteza Aghmesheh,(unknown),Michael Friedländer,Jahn M. Nesland,J. Kærn,Michael Stewart,kConFab,Anne Dørum,Kathy Tucker,Michael F. Buckley	2
15	The 10q24‐linked split hand/split foot syndrome (SHFM3): Narrowing of the critical region and confirmation of the clinical phenotype 2003 ·American Journal of Medical Genetics Part A ·Tony Roscioli,Peter J. Taylor,(unknown),Jennifer A. Donald,J. Masel,Ian A. Glass,Michael F. Buckley	12
16	In utero fetal muscle biopsy in the diagnosis of Duchenne muscular dystrophy 2002 ·Australian and New Zealand Journal of Obstetrics and Gynaecology ·(unknown),David Mowat,Vivienne Tobias,Peter J. Taylor,Michael F. Buckley,(unknown),Daniel Challis	3
17	VAX/VMS event monitoring and analysis 2002 ·Michael F. Buckley,Daniel P. Siewiorek	22
18	Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG‐interruption pattern in Asian populations 2001 ·Annals of Human Genetics ·Sultana MH Faradz,Jayne Leggo,Anna Murray,P.R.L.C. Lam-Po-Tang,Michael F. Buckley,Jeanette J. A. Holden	7
19	Genetic diversity at the FMR1 locus in the Indonesian population 2000 ·Annals of Human Genetics ·Sultana MH Faradz,(unknown),Don Leigh,Mark A. Jenkins,Jayne Leggo,Michael F. Buckley,Jeanette J. A. Holden	19
20	Preparation of bacteriophage λ DNA using the TL-100 ultracentrifuge 1988 ·Analytical Biochemistry ·Michael F. Buckley,James W. Goding	5

About Michael F. Buckley

Michael F. Buckley is a scholar working on Developmental Biology, Genetics and Software, having authored 32 papers that have together received 701 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Prenatal Screening and Diagnostics (4 papers) and Craniofacial Disorders and Treatments (4 papers). The work is most often cited by research in Physiology (57 citations), Genetics (227 citations) and Software (30 citations). Michael F. Buckley has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include James W. Goding, Daniel P. Siewiorek, Tony Roscioli, William J. McKinstry, Kate L. Loveland, O. Margaret Garson, Hans Scheffer, Erik‐Jan Kamsteeg, Marianne Schwartz and Wolfram Kreß. Their work appears in journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Circulation Research.

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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