Mathias Chiano

1.9k citations

26 papers · 1.3k indexed · h-index 15

Impact in

Genetics top 5%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
Nephrology top 5%
- Parathyroid Disorders and Treatments

Papers in

Anatomy 1
Genetics 16
- Genetic Associations and Epidemiology 10
- Genomic variations and chromosomal abnormalities 6
- Genetic Mapping and Diversity in Plants and Animals 3
- BRCA gene mutations in cancer 2

Co-authors: David Clayton Alison M. Dunning David Craufurd Gail Norbury Jayne Leggo Elisabeth Rosser David C. Rubinsztein Sylvie Mazoyer
Journals: Annals of Human Genetics (3 papers)Human Molecular Genetics (3 papers)Journal of Bone and Mineral Research (3 papers)Respiratory Medicine (2 papers)Osteoarthritis and Cartilage (2 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

Mathias Chiano

26 papers receiving 1.3k citations

Peers

Countries citing papers authored by Mathias Chiano

Since Specialization

Citations

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

Fields of papers citing papers by Mathias Chiano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Genetics plays a limited role in predicting chronic obstructive pulmonary disease treatment response and exacerbation Respiratory Medicine ·Louise K. Hosking, Astrid Yeo, Joshua Hoffman, Mathias Chiano, Dana J. Fraser, Soumitra Ghosh, David A. Lipson, Neil Martin, Lynn D. Condreay, Charles Cox, Pamela St. Jean	2021	6
2	Phenome-wide association study using research participants’ self-reported data provides insight into the Th17 and IL-17 pathway PLoS ONE ·Margaret G. Ehm, Jennifer L. Aponte, Mathias Chiano, Laura M. Yerges-Armstrong, Toby Johnson, Juliet N. Barker, Suzanne F. Cook, Manuel Figueroa-Gonzalez, David A. Hinds, Li Li, Matthew R. Nelson, Michael A. Simpson, Chao Tian, Linda McCarthy, Deepak K. Rajpal, Dawn Waterworth	2017	10
3	No genetic association detected with mepolizumab efficacy in severe asthma Respiratory Medicine ·Lynn D. Condreay, Mathias Chiano, Héctor Ortega, Natalie Buchan, 정명주, Eugene R. Bleecker, Philip J. Thompson, Marc Humbert, Peter G. Gibson, Steven W. Yancey, Soumitra Ghosh	2017	14
4	‘Sifting the significance from the data’ - the impact of high-throughput genomic technologies on human genetics and health care Human Genomics ·Angus Clarke, D.N. Cooper, Michael Krawczak, Chris Tyler‐Smith, Helen M. Wallace, Andrew O.M. Wilkie, Anis Rochma Pratiwi, Ruth Chadwick, Nick Craddock, Rosalind M. John, John Gallacher, Mathias Chiano	2012	5
5	Pharmacogenetic investigation of lapatinib-associated diarrhea in metastatic breast cancer clinical trials. Journal of Clinical Oncology ·Linda P. Briley, Mathias Chiano, Karen S. King, Ketil Grong, A. Preston, Francisco Sapunar, Vincent Mooser, Lon R. Cardon, Colin F. Spraggs	2011	1
6	Identification of a novel asthma susceptibility gene on chromosome 1qter and its functional evaluation Human Molecular Genetics ·John H. White, Mathias Chiano, Mark Wigglesworth, Robert S. Geske, J. Riley, Nicholas J. White, Sue Hall, Guohua Zhu, Hans Dieter Flach, Thomas F. Savage, W. J. Anderson, Ayşe Nur Yeksan, Monika Ducceschi, (unknown), Jørgen Vestbo, F. Blocher	2008	50
7	Absence of association of asporin polymorphisms and osteoarthritis susceptibility in US Caucasians Osteoarthritis and Cartilage ·Hurbert Kazoora, Van de Walle S, Jennifer L. Aponte, V. Ramdan, Stefen Brady, Virginia B. Kraus, Joanne M. Jordan, Michael Doherty, Anthony G. Wilson, R. W. Moskowitz, Mark S. Hochberg, Richard F. Loeser, Jordan B. Renner, Mathias Chiano	2008	27
8	A48 GENOME-WIDE LINKAGE SCAN AND HIGH-DENSITY ASSOCIATION STUDIES IMPLICATE CHROMOSOME 18q21 WITH GENERALIZED OSTEOARTHRITIS Osteoarthritis and Cartilage ·Joanne M. Jordan, Hurbert Kazoora, Mathias Chiano, Michael Doherty, Marc C. Hochberg, Virginia B. Kraus, Richard F. Loeser, R. W. Moskowitz, DG Dagmar Buzeman	2008	4
9	A coding polymorphism in the CYSLT2 receptor with reduced affinity to LTD4 is associated with asthma Pharmacogenetics ·Sreekumar Pillai, Diane J. Cousens, Ashley Barnes, Peter T. Buckley, Mathias Chiano, Louise K. Hosking, Francis Miliany Canela da Silva, Mary E. Fling, James J. Foley, Andrew R. Green, Henry M. Sarau, Dulcie B. Schmidt, Catherine S. Sprankle, Malcolm N. Blumenthal, Jørgen Vestbo, Yann Drèze, William E. Wixted, Tânia Isabel Moreira Gonçalves, Wayne H. Anderson, Diane M. Ignar	2004	48
10	Novel association suggests multiple independent QTLs within chromosome 5q21–33 region control variation in total humans IgE levels Genes and Immunity ·Kourosh R. Ahmadi, Jerry S. Lanchbury, Gang-Seong Kim, Mathias Chiano, D B Thompson, Oscar Alejandro Garces-Mares, Fred Mathew Toboso Otsyeno, K. Thraede, Hannah J. Wong, David P. Strachan, Tim D. Spector	2003	14
11	Comparison of Genome Screens for Two Independent Cohorts Provides Replication of Suggestive Linkage of Bone Mineral Density to 3p21 and 1p36 The American Journal of Human Genetics ·Scott G. Wilson, Peter Reed, Aruna T. Bansal, Mathias Chiano, Dan Iudean, Maksim Matyuta, Richard L. Prince, D B Thompson, Elizabeth Thompson, Mark E.S. Bailey, Patrick W. Kleyn, Philip N. Sambrook, M. Shi, Tim D. Spector	2003	119
12	Genetic Analysis of Complex Traits Humana Press eBooks ·Stephen P. Bryant, Mathias Chiano	2003	3
13	Large-scale genome-wide screen of female twin pairs confirms presence of QTLs for BMD at 1p36 and 3p21 Journal of Bone and Mineral Research ·Gorichkina La, Peter Reed, Mathias Chiano, Meisen Shi, Jay B. Lichter, Maksim Matyuta, Tim D. Spector	2002	2
14	Sib‐TDT analysis of human TGF‐β1 gene single nucleotide polymorphisms in female twins: evidence for linkage and association with blood pressure at the codon 263 polymorphism Research Portal (King's College London) ·Harold Snieder, В.О. Таргульян, Mathias Chiano, Alex J. MacGregor, TD Spector	2000	7
15	Genotypic relative risks under ordered restriction Genetic Epidemiology ·Mathias Chiano, David Clayton	1998	13
16	Fine genetic mapping using haplotype analysis and the missing data problem Annals of Human Genetics ·Mathias Chiano, David Clayton	1998	72
17	Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease Proceedings of the National Academy of Sciences ·David C. Rubinsztein, Jayne Leggo, Mathias Chiano, M Funt, Gail Norbury, Elisabeth Rosser, David Craufurd	1997	181
18	Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation Nature Genetics ·Simon A. Gayther, William Warren, Sylvie Mazoyer, Paul A. Russell, Patricia Harrington, Mathias Chiano, Sheila Seal, Rifat Hamoudi, Elizabeth J. van Rensburg, Alison M. Dunning, Richard R. Love, D. Gareth Evans, Doug Easton, David Clayton, Michael R. Stratton, Bruce A.J. Ponder	1995	376
19	Linkage detection under heterogeneity and the mixture problem Annals of Human Genetics ·Mathias Chiano, John R.W. Yates	1995	16
20	Bootstrapping in human genetic linkage Annals of Human Genetics ·Mathias Chiano, John R.W. Yates	1994	10

About Mathias Chiano

Mathias Chiano is a scholar working on Anatomy, Genetics, Rheumatology, Orthopedics and Sports Medicine and Dermatology, having authored 26 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (6 papers), Asthma and respiratory diseases (5 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers), Gene expression and cancer classification (3 papers), Mitochondrial Function and Pathology (2 papers), BRCA gene mutations in cancer (2 papers) and Respiratory and Cough-Related Research (2 papers). The work is most often cited by research in Genetics (677 citations), Nephrology (116 citations), Reproductive Medicine (121 citations), Orthopedics and Sports Medicine (100 citations) and Cellular and Molecular Neuroscience (200 citations). Mathias Chiano has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include David Clayton, Alison M. Dunning, David Craufurd, Gail Norbury, Jayne Leggo, Elisabeth Rosser, David C. Rubinsztein, Sylvie Mazoyer, D. Gareth Evans and Simon A. Gayther. Their work appears in journals such as Annals of Human Genetics, Human Molecular Genetics, Journal of Bone and Mineral Research, Respiratory Medicine and Osteoarthritis and Cartilage.

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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