Andrew P. Boright

3.1k citations

18 papers · 1.2k indexed · h-index 13

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Hematology top 10%
- Blood groups and transfusion

Papers in

Clinical Biochemistry 3
- Paraoxonase enzyme and polymorphisms 2
Nephrology 3
- Chronic Kidney Disease and Diabetes 3

Co-authors: Stephen W. Scherer Andrew D. Paterson Shelley B. Bull Lei Sun Lap‐Chee Tsui S. Mohsen Hosseini Lucia Mirea Ikuko Kondo
Journals: Diabetes (3 papers)Atherosclerosis (2 papers)Human Genetics (2 papers)The American Journal of Human Genetics (1 paper)Nature Genetics (1 paper)
Partner nations: Canada United States Austria

In The Last Decade

Andrew P. Boright

17 papers receiving 1.2k citations

Peers

Countries citing papers authored by Andrew P. Boright

Since Specialization

Citations

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

Fields of papers citing papers by Andrew P. Boright

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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18 of 18 papers shown

#	Work
1	The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy Human Genetics ·S. Mohsen Hosseini, Andrew P. Boright, Lei Sun, Angelo J. Canty, Shelley B. Bull, Ronald Klein, Andrew D. Paterson	2014	48
2	The associations of apolipoprotein E and angiotensin‐converting enzyme polymorphisms and cognitive function in Type 1 diabetes based on an 18‐year follow‐up of the DCCT cohort Diabetic Medicine ·A. Jacobson, Andrew D. Paterson, Christopher M. Ryan, Patricia A. Cleary, Barbara H. Waberski, Katie Weinger, Gail Musen, William T. Dahms, Guido Sorelli, N. Silvers, J. Harth, Andrew P. Boright	2009	12
3	Genome-Wide Association Identifies the ABO Blood Group as a Major Locus Associated With Serum Levels of Soluble E-Selectin Arteriosclerosis Thrombosis and Vascular Biology ·Andrew D. Paterson, Maria F. Lopes‐Virella, Daryl Waggott, Andrew P. Boright, S. Mohsen Hosseini, Rickey E. Carter, T.K. Blackburn, Lucia Mirea, Bhupinder Bharaj, Lei Sun, Shelley B. Bull	2009	156
4	A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose Diabetes ·Andrew D. Paterson, Daryl Waggott, Andrew P. Boright, S. Mohsen Hosseini, T.K. Blackburn, Marie‐Pierre Sylvestre, Stacey Lezama, Bhupinder Bharaj, Patricia A. Cleary, John M. Lachin, Jennifer E. Below, Dan L. Nicolae, Nancy J. Cox, Angelo J. Canty, Lei Sun, Shelley B. Bull	2009	82
5	Multiple Variants in Vascular Endothelial Growth Factor (VEGFA) Are Risk Factors for Time to Severe Retinopathy in Type 1 Diabetes Diabetes ·Hussam Al‐Kateb, Lucia Mirea, 周宗强, Lei Sun, Xiaoqing Liu, Hongtao Chen, Shelley B. Bull, Andrew P. Boright, Andrew D. Paterson	2007	80
6	LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes Atherosclerosis ·Susan J. Murdoch, Andrew P. Boright, Andrew D. Paterson, Bernard Zinman, Michael W. Steffes, Patricia A. Cleary, Karen L. Edwards, Santica Marcovina, Jonathan Q. Purnell, John D. Brunzell	2006	13
7	Genetic Variation at the ACE Gene Is Associated With Persistent Microalbuminuria and Severe Nephropathy in Type 1 Diabetes Diabetes ·Andrew P. Boright, Andrew D. Paterson, Lucia Mirea, Shelley B. Bull, S. V. Ariyaratnam, Stephen W. Scherer, Bernard Zinman	2005	74
8	Genescript: DNA sequence annotation pipeline Bioinformatics ·Alexander K. Hudek, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer	2003	7
9	Genomics and Pediatric Research Pediatric Research ·Andrew P. Boright, Juha Kere, Stephen W. Scherer	2003	1
10	Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome The American Journal of Human Genetics ·Erwin Petek, Christian Windpassinger, Seftiani Cahyaningsih, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer, Sugiharto Sugiharto, Klaus W. Wagner	2001	130
11	Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations Oncogene ·Martin Corcoran, Sarah Mould, Jennifer Orchard, Rachel Ibbotson, Robert M. Chapman, Andrew P. Boright, Craig D. Platt, V. Zaynullin, Stephen W. Scherer, David Oscier	1999	108
12	The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein Nature Genetics ·Keiko Kobayashi, David S. Sinasac, Mikio Iijima, Andrew P. Boright, Laila Begum, Jeffrey R. Lee, Tomotsugu Yasuda, Sayaka Ikeda, Ryuki Hirano, Hiroki Terazono, Michael A. Crackower, Ikuko Kondo, Lap‐Chee Tsui, Stephen W. Scherer, Takeyori Saheki	1999	326
13	Large-Scale Sequencing of Two Regions in Human Chromosome 7q22: Analysis of 650 kb of Genomic Sequence around the EPO and CUTL1 Loci Reveals 17 Genes Genome Research ·Gernot Glöckner, Stephen W. Scherer, Ying-Bo SONG, Andrew P. Boright, Jacqueline Weber, Lap Chee Tsui, André Rosenthal	1998	50
14	Association and linkage of LDLR gene variation with variation in plasma low density lipoprotein cholesterol Journal of Human Genetics ·Andrew P. Boright, Philip W. Connelly, Jason Brunt, Kenneth Morgan, Robert A. Hegele	1998	31
15	Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites Atherosclerosis ·Andrew P. Boright, Philip W. Connelly, Jason Brunt, Stephen W. Scherer, Lap‐Chee Tsui, Robert A. Hegele	1998	58
16	F5 Q506 mutation and the low prevalence of cardiovascular disease in Canadian Inuit. PubMed ·Livia Martins del Bosco, Philip W. Connelly, Andrew P. Boright, Young Tk, Mohsen Moshkbide Haghighi	1998	7
17	Prolidase deficiency: biochemical classification of alleles. PubMed ·Andrew P. Boright, C R Scriver, Azhar Hanif, Francis Y.M. Choy	1989	32
18	Osteogenesis imperfecta: a heterogeneous morphologic phenotype in cultured dermal fibroblasts Human Genetics ·Andrew P. Boright, Gerald Lancaster, Charles R. Scriver	1984	1

About Andrew P. Boright

Andrew P. Boright is a scholar working on Clinical Biochemistry, Nephrology, Endocrinology, Diabetes and Metabolism, Ophthalmology and Genetics, having authored 18 papers that have together received 1.2k indexed citations. Recurring topics across this work include Chronic Kidney Disease and Diabetes (3 papers), Chronic Lymphocytic Leukemia Research (2 papers), Retinal Diseases and Treatments (2 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (2 papers), Ubiquitin and proteasome pathways (2 papers), Paraoxonase enzyme and polymorphisms (2 papers), Diabetes Treatment and Management (2 papers) and Pancreatic function and diabetes (2 papers). The work is most often cited by research in Clinical Biochemistry (386 citations), Hematology (144 citations), Biochemistry (92 citations), Genetics (108 citations) and Ophthalmology (81 citations). Andrew P. Boright has collaborated with scholars based in Canada, United States and Austria. Frequent co-authors include Stephen W. Scherer, Andrew D. Paterson, Shelley B. Bull, Lei Sun, Lap‐Chee Tsui, S. Mohsen Hosseini, Lucia Mirea, Ikuko Kondo, Laila Begum and Ryuki Hirano. Their work appears in journals such as Diabetes, Atherosclerosis, Human Genetics, The American Journal of Human Genetics 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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