Matthew B. Lanktree

7.0k total citations · 1 hit paper
74 papers, 1.9k citations indexed

About

Matthew B. Lanktree is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Matthew B. Lanktree has authored 74 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 28 papers in Molecular Biology and 13 papers in Nephrology. Recurrent topics in Matthew B. Lanktree's work include Genetic Associations and Epidemiology (16 papers), Genetic and Kidney Cyst Diseases (15 papers) and Renal and related cancers (10 papers). Matthew B. Lanktree is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Genetic and Kidney Cyst Diseases (15 papers) and Renal and related cancers (10 papers). Matthew B. Lanktree collaborates with scholars based in Canada, United States and Germany. Matthew B. Lanktree's co-authors include Robert A. Hegele, York Pei, Salim Yusuf, Sonia S. Anand, Xuewen Song, Amirreza Haghighi, Guillaume Paré, Arlene B. Chapman, Elsa Guiard and Andrew D. Paterson and has published in prestigious journals such as Blood, Bioinformatics and Journal of the American College of Cardiology.

In The Last Decade

Matthew B. Lanktree

67 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Endoplasmic reticulum stress as a driver and therapeutic target for kidney disease

2025 16 citations Jae Hyun Byun, Paul Lebeau et al. Nature Reviews Nephrology profile →

Peers

Matthew B. Lanktree

GENET

SURGE

CCM

HEMAT

Dermot F. Reilly United States

Thomas C. Resta United States

J. D. Firth United Kingdom

Vardiella Meiner Israel

Jindong Chen China

Aris Baras United States

Alexander Paliege Germany

Claudia Giambartolomei United States

Joshua C. Bis United States

Maggie C. Y. Ng United States

Dermot F. Reilly United States

Matthew B. Lanktree

272 ×0.3

GENET

476 ×0.7

212 ×0.7

SURGE

269 ×1.1

CCM

189 ×1.1

HEMAT

Citations per year, relative to Matthew B. Lanktree Matthew B. Lanktree (= 1×) peers Dermot F. Reilly

Countries citing papers authored by Matthew B. Lanktree

Since Specialization

Citations

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

Fields of papers citing papers by Matthew B. Lanktree

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew B. Lanktree

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew B. Lanktree. A scholar is included among the top collaborators of Matthew B. Lanktree 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 B. Lanktree. Matthew B. Lanktree 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

Byun, Jae Hyun, Paul Lebeau, Nikhil Uppal, et al.. (2025). Endoplasmic reticulum stress as a driver and therapeutic target for kidney disease. Nature Reviews Nephrology. 21(5). 299–313. 16 indexed citations breakdown →

Wu, Jianhan, Caitlyn Vlasschaert, Ricky Lali, et al.. (2024). Kidney Volume and Risk of Incident Kidney Outcomes. Journal of the American Society of Nephrology. 35(9). 1240–1251. 3 indexed citations

Voth, Jennifer, et al.. (2024). Whole body resistance training on functional outcomes of patients with Stage 4 or 5 chronic kidney disease: A systematic review. Physiological Reports. 12(15). e16151–e16151. 1 indexed citations

Vlasschaert, Caitlyn, Taralynn Mack, J. Brett Heimlich, et al.. (2023). A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic datasets. Blood. 141(18). 2214–2223. 74 indexed citations

Lanktree, Matthew B., Nicolas Perrot, Andrew Smyth, et al.. (2023). A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation. Kidney International. 104(6). 1170–1184. 12 indexed citations

Lanktree, Matthew B., et al.. (2023). Proteome-Wide Changes in Blood Biomarkers During Hemodialysis. Kidney International Reports. 9(1). 177–181. 1 indexed citations

Vlasschaert, Caitlyn, Amy J. M. McNaughton, Michael Chong, et al.. (2022). Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney Disease. Journal of the American Society of Nephrology. 33(5). 985–995. 61 indexed citations

Mohammadi‐Shemirani, Pedrum, Michael Chong, Sukrit Narula, et al.. (2022). Elevated Lipoprotein(a) and Risk of Atrial Fibrillation. Journal of the American College of Cardiology. 79(16). 1579–1590. 63 indexed citations

Vlasschaert, Caitlyn, Michael J. Rauh, & Matthew B. Lanktree. (2022). Response to: “Clonal Hematopoiesis of Indeterminate Potential and Diabetic Kidney Disease: A Nested Case-Control Study”. Kidney International Reports. 7(11). 2543–2543. 4 indexed citations

10.

Lanktree, Matthew B., Amirreza Haghighi, Elsa Guiard, et al.. (2018). Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing. Journal of the American Society of Nephrology. 29(10). 2593–2600. 181 indexed citations

11.

Lanktree, Matthew B. & Arlene B. Chapman. (2017). New treatment paradigms for ADPKD: moving towards precision medicine. Nature Reviews Nephrology. 13(12). 750–768. 56 indexed citations

12.

Lanktree, Matthew B., Sébastien Thériault, Michael Walsh, & Guillaume Paré. (2017). HDL Cholesterol, LDL Cholesterol, and Triglycerides as Risk Factors for CKD: A Mendelian Randomization Study. American Journal of Kidney Diseases. 71(2). 166–172. 87 indexed citations

13.

Lanktree, Matthew B., Clara C. Elbers, Yun Li, et al.. (2015). Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration. Journal of Lipid Research. 56(9). 1781–1786. 7 indexed citations

14.

Lanktree, Matthew B., Bekim Sadiković, & Mark Crowther. (2014). A 42-year-old man with elevated ferritin. Canadian Medical Association Journal. 187(11). 820–821. 1 indexed citations

15.

Lanktree, Matthew B., Christopher T. Johansen, Tisha Joy, & Robert A. Hegele. (2010). A Translational View of the Genetics of Lipodystrophy and Ectopic Fat Deposition. Progress in molecular biology and translational science. 94. 159–196. 11 indexed citations

16.

Lahiry, Piya, Jian Wang, J. F. Robinson, et al.. (2009). A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems. The American Journal of Human Genetics. 84(6). 822–822. 5 indexed citations

17.

Lanktree, Matthew B., Alessio Squassina, John S. Strauss, et al.. (2008). Association study of brain‐derived neurotrophic factor (BDNF) and LIN‐7 homolog (LIN‐7) genes with adult attention‐deficit/hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 945–951. 40 indexed citations

18.

Lanktree, Matthew B. & Robert A. Hegele. (2008). Copy number variation in metabolic phenotypes. Cytogenetic and Genome Research. 123(1-4). 169–175. 15 indexed citations

19.

Shinkai, Takahiro, Vincenzo De Luca, Rudi Hwang, et al.. (2007). Association analyses of the DAOA/G30 and d-amino-acid oxidase genes in schizophrenia: Further evidence for a role in schizophrenia. NeuroMolecular Medicine. 9(2). 169–177. 38 indexed citations

20.

Squassina, Alessio, Matthew B. Lanktree, Vincenzo De Luca, et al.. (2007). Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder. Neuroscience Letters. 432(1). 50–53. 11 indexed citations

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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