Brendan Lee

21.7k total citations · 1 hit paper
224 papers, 10.5k citations indexed

About

Brendan Lee is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Brendan Lee has authored 224 papers receiving a total of 10.5k indexed citations (citations by other indexed papers that have themselves been cited), including 116 papers in Genetics, 109 papers in Molecular Biology and 39 papers in Rheumatology. Recurrent topics in Brendan Lee's work include Connective tissue disorders research (72 papers), Bone and Dental Protein Studies (21 papers) and Metabolism and Genetic Disorders (20 papers). Brendan Lee is often cited by papers focused on Connective tissue disorders research (72 papers), Bone and Dental Protein Studies (21 papers) and Metabolism and Genetic Disorders (20 papers). Brendan Lee collaborates with scholars based in United States, Canada and Germany. Brendan Lee's co-authors include Terry Bertin, Elda Munivez, Guang Zhou, Francesco Ramirez, Roy Morello, Ingo Grafe, Tao Yang, Philippe M. Campeau, Antonio Baldini and Feyza Engin and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Brendan Lee

216 papers receiving 10.3k 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.

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

1991 515 citations Brendan Lee et al. profile →

Peers

Countries citing papers authored by Brendan Lee

Since Specialization

Citations

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

Fields of papers citing papers by Brendan Lee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brendan Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Brendan Lee. A scholar is included among the top collaborators of Brendan Lee 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 Brendan Lee. Brendan Lee 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

#	Title	Journal	Authors	Indexed citations
1	Clinical validation of RNA sequencing for Mendelian disorder diagnostics	The American Journal of Human Genetics	Sen Zhao, Hongzheng Dai et al.	7
2	The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics	The American Journal of Human Genetics	Sen Zhao, Shenglan Li et al.	0
3	Genetic Evaluation for Monogenic Disorders of Low Bone Mass and Increased Bone Fragility: What Clinicians Need to Know	Current Osteoporosis Reports	Brendan Lee, Sandesh C.S. Nagamani et al.	0
4	Development and evaluation of a training curriculum to engage researchers on accessing and analyzing the All of Us data	Journal of the American Medical Informatics Association	Shamika Ketkar, Ashley M. Butler et al.	2
5	Delayed skeletal development and IGF-1 deficiency in a mouse model of lysinuric protein intolerance	Disease Models & Mechanisms	Bridget M. Stroup, Xiaohui Li et al.	1
6	De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities	American Journal of Medical Genetics Part A	Scott Ward, Paul J. Benke et al.	0
7	Argininosuccinate lyase deficiency causes blood-brain barrier disruption via nitric oxide–mediated dysregulation of claudin expression	JCI Insight	Urszula Polak, Ming‐Ming Jiang et al.	6
8	PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature	American Journal of Medical Genetics Part A	David R. Murdock, Lindsay C. Burrage et al.	2
9	Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta	Proceedings of the National Academy of Sciences	Joohyun Lim, Caressa Lietman et al.	7
10	A novel de novo intronic variant in ITPR1 causes Gillespie syndrome	American Journal of Medical Genetics Part A	Ming‐Ming Jiang, Xiaohui Li et al.	5
11	Tendon and motor phenotypes in the Crtap-/- mouse model of recessive osteogenesis imperfecta	eLife	Matthew W. Grol, Nele A Haelterman et al.	13
12	Evaluation of extracorporeal cardiopulmonary resuscitation eligibility criteria for out-of-hospital cardiac arrest patients	BMC Research Notes	Brendan Lee, Eric Sy et al.	0
13	Caries prevalence and experience in individuals with osteogenesis imperfecta: A cross‐sectional multicenter study	Special Care in Dentistry	Faleh Tamimi, Francis H. Glorieux et al.	12
14	Genetic Burden Contributing to Extremely Low or High Bone Mineral Density in a Senior Male Population From the Osteoporotic Fractures in Men Study (MrOS)	JBMR Plus	Shan Chen, Mahim Jain et al.	1
15	Whole‐Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI	JBMR Plus	Zixue Jin, Lindsay C. Burrage et al.	3
16	A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen	Journal of Bone and Mineral Research	Iván Durán, Jorge Martı́n et al.	56
17	Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis	Journal of Clinical Investigation	Kyu Sang Joeng, Joohyun Lim et al.	140
18	mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development	Scientific Reports	Joohyun Lim, Elda Munivez et al.	21
19	Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation	Journal of Clinical Investigation	Jeffrey H. Miner, Roy Morello et al.	77
20	Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation	Journal of Clinical Investigation	Jeffrey H. Miner, Roy Morello et al.	10

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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