Brad T. Tinkle

5.2k total citations · 2 hit papers
16 papers, 2.3k citations indexed

About

Brad T. Tinkle is a scholar working on Genetics, Immunology and Rheumatology. According to data from OpenAlex, Brad T. Tinkle has authored 16 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Immunology and 3 papers in Rheumatology. Recurrent topics in Brad T. Tinkle's work include Connective tissue disorders research (7 papers), HIV Research and Treatment (2 papers) and Immune Cell Function and Interaction (2 papers). Brad T. Tinkle is often cited by papers focused on Connective tissue disorders research (7 papers), HIV Research and Treatment (2 papers) and Immune Cell Function and Interaction (2 papers). Brad T. Tinkle collaborates with scholars based in United States, United Kingdom and Belgium. Brad T. Tinkle's co-authors include C C Haudenschild, Rodney Grahame, Howard P. Levy, Marco Castori, Gregory D. Jay, Charles J. Bieberich, Frank M. LaFerla, Fransiska Malfait, M.B. Leon and Gene Liau and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Journal of Allergy and Clinical Immunology.

In The Last Decade

Brad T. Tinkle

16 papers receiving 2.3k 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.

A framework for the classification of joint hypermobility and related conditions

2017 370 citations Marco Castori, Brad T. Tinkle et al. American Journal of Medical Genetics Part C Seminars in Medical Genetics profile →
Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history

2017 317 citations Brad T. Tinkle, Marco Castori et al. American Journal of Medical Genetics Part C Seminars in Medical Genetics profile →

Peers

Countries citing papers authored by Brad T. Tinkle

Since Specialization

Citations

This map shows the geographic impact of Brad T. Tinkle'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 Brad T. Tinkle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brad T. Tinkle more than expected).

Fields of papers citing papers by Brad T. Tinkle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brad T. Tinkle. 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 Brad T. Tinkle. The network helps show where Brad T. Tinkle may publish in the future.

Co-authorship network of co-authors of Brad T. Tinkle

This figure shows the co-authorship network connecting the top 25 collaborators of Brad T. Tinkle. A scholar is included among the top collaborators of Brad T. Tinkle 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 Brad T. Tinkle. Brad T. Tinkle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome 2021 ·Human Mutation ·(unknown), Tim Van Damme, Delfien Syx, Laura Muiño Mosquera, Sheela Nampoothiri, (unknown), Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, M Bonduelle, Isabelle Migeotte, (unknown), Serdar Ceylaner, (unknown), Brad T. Tinkle, Sofie Symoens, Fransiska Malfait	18
2	Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history breakdown → 2017 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Brad T. Tinkle, Marco Castori, Britta Berglund, Helen Cohen, Rodney Grahame, Hanadi Kazkaz, Howard P. Levy	317
3	A framework for the classification of joint hypermobility and related conditions breakdown → 2017 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Marco Castori, Brad T. Tinkle, Howard P. Levy, Rodney Grahame, Fransiska Malfait, Alan J. Hakim	370
4	Pain management in the Ehlers–Danlos syndromes 2017 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Pradeep Chopra, Brad T. Tinkle, C. Hamonet, (unknown), Anne Gompel, Antonio Bulbena, Clair A. Francomano	122
5	The international consortium on the Ehlers–Danlos syndromes 2017 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Lara Bloom, Peter H. Byers, Clair A. Francomano, Brad T. Tinkle, Fransiska Malfait	64
6	High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders 2013 ·Journal of Allergy and Clinical Immunology ·J. Pablo Abonia, Ting Wen, Emily M. Stucke, (unknown), Molly S. Griffith, Katherine A. Kemme, Margaret H. Collins, Philip E. Putnam, James P. Franciosi, Karl F. von Tiehl, Brad T. Tinkle, Keith Marsolo, Lisa J. Martin, Stephanie M. Ware, Marc E. Rothenberg	138
7	Performance Evaluation of the Next‐Generation Sequencing Approach for Molecular Diagnosis of Hereditary Hearing Loss 2013 ·Otolaryngology ·Theru A. Sivakumaran, Ammar Husami, Diane Kissell, Wenying Zhang, Mehdi Keddache, (unknown), Brad T. Tinkle, John H. Greinwald, Kejian Zhang	28
8	Variable expression of neurofibromatosis 1 in monozygotic twins 2011 ·American Journal of Medical Genetics Part A ·(unknown), David A. Stevenson, David Viskochil, Brad T. Tinkle, Lisa J. Martin, Elizabeth K. Schorry	41
9	Cross-Sectional and Longitudinal Assessment of Aortic Root Dilation and Valvular Anomalies in Hypermobile and Classic Ehlers-Danlos Syndrome 2010 ·The Journal of Pediatrics ·Carrie Atzinger, Richard A. Meyer, Philip R. Khoury, Zhiqian Gao, Brad T. Tinkle	48
10	The lack of clinical distinction between the hypermobility type of Ehlers–Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome) 2009 ·American Journal of Medical Genetics Part A ·Brad T. Tinkle, Howard Bird, Rodney Grahame, Mark E. Lavallee, Howard P. Levy, David Sillence	238
11	Long‐term survival in a patient with del(18)(q12.2q21.1) 2003 ·American Journal of Medical Genetics Part A ·Brad T. Tinkle, Carol A. Christianson, Elizabeth K. Schorry, (unknown), Robert J. Hopkin	20
12	Transgenic dissection of HIV genes involved in lymphoid depletion. 1997 ·Journal of Clinical Investigation ·Brad T. Tinkle, Hiroyuki Ueda, Lien T. Ngo, Paul A. Luciw, Kathryn Shaw, C A Rosen, Gregory D. Jay	16
13	The Alzheimer's Aβ peptide induces neurodegeneration and apoptotic cell death in transgenic mice 1995 ·Nature Genetics ·Frank M. LaFerla, Brad T. Tinkle, Charles J. Bieberich, C C Haudenschild, Gregory D. Jay	435
14	The Pathogenic Role of Human Immunodeficiency Virus Accessory Genes in Transgenic Mice 1995 ·Current topics in microbiology and immunology ·Brad T. Tinkle, Hiroyuki Ueda, Gregory D. Jay	2
15	Evidence for apoptosis in human atherogenesis and in a rat vascular injury model. 1995 ·PubMed ·David K. Han, C C Haudenschild, Minha Hong, Brad T. Tinkle, M.B. Leon, Gene Liau	431
16	A Transgenic Model of Transactivation by the Tax Protein of HTLV-I 1993 ·Virology ·Charles J. Bieberich, (unknown), Brad T. Tinkle, Gregory D. Jay	26

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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