Matthew P. Johnson

6.8k citations

64 papers · 2.4k indexed · h-index 26

Molecular Biology top 10%
Obstetrics and Gynecology top 1%
Genetics top 5%
Pediatrics, Perinatology and Child Health top 2%
Immunology top 10%

Co-authors: Eric K. Moses John Blangero Thomas D. Dyer Joanne E. Curran Harald H.H. Göring Shaun P. Brennecke Laura Almasy Jeremy B. M. Jowett
Topics: Pregnancy and preeclampsia studies (23 papers)Birth, Development, and Health (13 papers)Genetic Associations and Epidemiology (7 papers)
Cited by: Obstetrics and Gynecology Pediatrics, Perinatology and Child Health Immunology
Journals: The Lancet Nucleic Acids Research Nature Genetics
Partner nations: United States Australia Norway

In The Last Decade

Matthew P. Johnson

62 papers receiving 2.4k citations

Peers

Countries citing papers authored by Matthew P. Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Matthew P. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew P. Johnson. 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 Matthew P. Johnson. The network helps show where Matthew P. Johnson may publish in the future.

Co-authorship network of co-authors of Matthew P. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew P. Johnson. A scholar is included among the top collaborators of Matthew P. Johnson 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 Matthew P. Johnson. Matthew P. Johnson 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	ADAM19: A Novel Target for Metabolic Syndrome in Humans and Mice 2017 ·Mediators of Inflammation ·(unknown),Caroline Rudnicka,(unknown),Joanne E. Curran,Matthew P. Johnson,Eric K. Moses,Harald H.H. Göring,John Blangero,Jana Hricová,Markus P. Schlaich,Vance B. Matthews	10
2	TRAK2, a novel regulator of ABCA1 expression, cholesterol efflux and HDL biogenesis 2017 ·European Heart Journal ·Nicole J. Lake,Rachael L. Taylor,(unknown),K N Harikrishnan,Joanne E. Curran,Marcio Almeida,Hemant Kulkarni,Nigora Mukhamedova,Anh Hoang,Hann Low,Andrew Murphy,Matthew P. Johnson,Thomas D. Dyer,Michael C. Mahaney,Harald H.H. Göring,Eric K. Moses,Dmitri Sviridov,John Blangero,Jeremy B. M. Jowett,Kiymet Bozaoglu	27
3	Soluble Forms of Intercellular and Vascular Cell Adhesion Molecules Independently Predict Progression to Type 2 Diabetes in Mexican American Families 2016 ·PLoS ONE ·Hemant Kulkarni,Manju Mamtani,Juan M. Peralta,Marcio Almeida,Thomas D. Dyer,Harald H.H. Göring,Matthew P. Johnson,Ravindranath Duggirala,Michael C. Mahaney,Rene L. Olvera,Laura Almasy,David C. Glahn,Sarah Williams‐Blangero,Joanne E. Curran,John Blangero	8
4	Effects of copy number variable regions on local gene expression in white blood cells of Mexican Americans 2015 ·European Journal of Human Genetics ·(unknown),Marcio Almeida,(unknown),Joanne E. Curran,Matthew P. Johnson,Eric K. Moses,Lawrence J. Abraham,Melanie A. Carless,Thomas D. Dyer,Satish Kumar,Laura Almasy,Michael C. Mahaney,Anthony G. Comuzzie,Sarah Williams‐Blangero,John Blangero,Donna M. Lehman,Harald H.H. Göring	6
5	Genome-Wide Transcriptome Directed Pathway Analysis of Maternal Pre-Eclampsia Susceptibility Genes 2015 ·PLoS ONE ·Hannah E. J. Yong,Phillip E. Melton,Matthew P. Johnson,Katy A. Freed,Bill Kalionis,Padma Murthi,Shaun P. Brennecke,Rosemary J. Keogh,Eric K. Moses	57
6	Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans 2013 ·Frontiers in Genetics ·V. Saroja Voruganti,Jack W. Kent,Subrata Debnath,Shelley A. Cole,Karin Haack,Harald H.H. Göring,Melanie A. Carless,Joanne E. Curran,Matthew P. Johnson,Laura Almasy,Thomas D. Dyer,Jean W. MacCluer,Eric K. Moses,Hanna E. Abboud,Michael C. Mahaney,John Blangero,Anthony G. Comuzzie	28
7	Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene 2012 ·PLoS ONE ·Matthew P. Johnson,Shaun P. Brennecke,Christine East,Harald H.H. Göring,Jack W. Kent,Thomas D. Dyer,Joanne Said,Linda T. Roten,Ann‐Charlotte Iversen,Lawrence J. Abraham,Seppo Heinonen,Eero Kajantie,Juha Kere,Katja Kivinen,Anneli Pouta,Hannele Laivuori,(unknown),Rigmor Austgulen,John Blangero,Eric K. Moses	96
8	OS077. The chromosome 2q22 preeclampsia susceptibility locus reveals shared novel risk factors for CVD 2012 ·Pregnancy Hypertension ·Eric K. Moses,Matthew P. Johnson,Christine East,Thomas D. Dyer,Linda T. Roten,J. Michael Proffitt,Mona Høysæter Fenstad,(unknown),Kaarin Mäkikallio,Seppo Heinonen,Eero Kajantie,Juha Kere,Hannele Laivuori,Rigmor Austgulen,John Blangero,Shaun P. Brennecke	2
9	OS046. Genome-wide association scans identify novel maternalsusceptibility loci for preeclampsia 2012 ·Pregnancy Hypertension ·Matthew P. Johnson,Shaun P. Brennecke,Ann‐Charlotte Iversen,Christine East,(unknown),Jack W. Kent,Tom Dyer,Joanne Said,Linda T. Roten,L.J. Abraham,(unknown),Bendik S. Winsvold,(unknown),Matthew J. Huentelman,Hans E. Krokan,Maiken E. Gabrielsen,Rigmor Austgulen,John Blangero,Eric K. Moses	2
10	Genotype×age interaction in human transcriptional ageing 2012 ·Mechanisms of Ageing and Development ·Jack W. Kent,Harald H.H. Göring,Jac Charlesworth,Eugene Drigalenko,Vincent P. Diego,Joanne E. Curran,Matthew P. Johnson,Thomas D. Dyer,Shelley A. Cole,Jeremy B. M. Jowett,Michael C. Mahaney,Anthony G. Comuzzie,Laura Almasy,Eric K. Moses,John Blangero,Sarah Williams‐Blangero	19
11	High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes 2011 ·Biological Psychiatry ·David C. Glahn,Joanne E. Curran,Anderson M. Winkler,Melanie A. Carless,Jack W. Kent,Jac Charlesworth,Matthew P. Johnson,Harald H.H. Göring,Shelley A. Cole,Thomas D. Dyer,Eric K. Moses,Rene L. Olvera,Peter Kochunov,Ravi Duggirala,Peter T. Fox,Laura Almasy,John Blangero	125
12	A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2) 2011 ·Molecular Human Reproduction ·Linda T. Roten,Mona Høysæter Fenstad,Siri Forsmo,Matthew P. Johnson,Eric K. Moses,Rigmor Austgulen,Frank Skorpen	43
13	Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease 2011 ·European Journal of Human Genetics ·Åsa Johansson,Joanne E. Curran,Matthew P. Johnson,Katy A. Freed,Mona Høysæter Fenstad,Line Bjørge,Irina P. Eide,Melanie A. Carless,David L. Rainwater,Harald H.H. Göring,Rigmor Austgulen,Eric K. Moses,John Blangero	32
14	STOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trondelag Health Study 2010 ·Molecular Human Reproduction ·Mona Høysæter Fenstad,Matthew P. Johnson,Mari Løset,(unknown),Linda T. Roten,Irina P. Eide,Line Bjørge,(unknown),Åsa Johansson,Thomas D. Dyer,Siri Forsmo,John Blangero,Eric K. Moses,Rigmor Austgulen	25
15	Molecular Markers of Preterm Labor in the Choriodecidua 2009 ·Reproductive Sciences ·(unknown),Matthew P. Johnson,Nicholas A. Williamson,Fiona Cullinane,Anthony W. Purcell,Eric K. Moses,Shaun P. Brennecke	43
16	Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia 2009 ·Molecular Human Reproduction ·Emer Fitzpatrick,Matthew P. Johnson,Thomas D. Dyer,S. M. Forrest,Kate Elliott,John Blangero,Shaun P. Brennecke,Eric K. Moses	34
17	Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study) 2008 ·European Journal of Human Genetics ·Linda T. Roten,Matthew P. Johnson,Siri Forsmo,Elizabeth M. Fitzpatrick,Thomas D. Dyer,Shaun P. Brennecke,John Blangero,Eric K. Moses,Rigmor Austgulen	50
18	Genetic determinants of mitochondrial content 2007 ·Human Molecular Genetics ·Joanne E. Curran,Matthew P. Johnson,Thomas D. Dyer,Harald H.H. Göring,Jack W. Kent,Jac Charlesworth,Anthony J. Borg,Jeremy B. M. Jowett,Shelley A. Cole,Jean W. MacCluer,Ahmed H. Kissebah,Eric K. Moses,John Blangero	44
19	A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibility 2005 ·QUT ePrints (Queensland University of Technology) ·Matthew P. Johnson,Rod A. Lea,Natalie Colson,(unknown),Lyn R. Griffiths	4
20	Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension 2001 ·Human Genetics ·(unknown),Matthew P. Johnson,Robert P. Curtain,Lyn R. Griffiths	31

About Matthew P. Johnson

Matthew P. Johnson is a scholar working on Obstetrics and Gynecology, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 64 papers that have together received 2.4k indexed citations. Recurring topics across this work include Pregnancy and preeclampsia studies (23 papers), Birth, Development, and Health (13 papers) and Genetic Associations and Epidemiology (7 papers). The work is most often cited by research in Obstetrics and Gynecology (533 citations), Pediatrics, Perinatology and Child Health (441 citations) and Immunology (372 citations). Matthew P. Johnson has collaborated with scholars based in United States, Australia and Norway. Frequent co-authors include Eric K. Moses, John Blangero, Thomas D. Dyer, Joanne E. Curran, Harald H.H. Göring, Shaun P. Brennecke, Laura Almasy, Jeremy B. M. Jowett, Rigmor Austgulen and Shelley A. Cole. Their work appears in journals such as The Lancet, Nucleic Acids Research and Nature 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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