Aileen M. Barnes

4.9k total citations · 1 hit paper
34 papers, 2.6k citations indexed

About

Aileen M. Barnes is a scholar working on Genetics, Rheumatology and Molecular Biology. According to data from OpenAlex, Aileen M. Barnes has authored 34 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 15 papers in Rheumatology and 11 papers in Molecular Biology. Recurrent topics in Aileen M. Barnes's work include Connective tissue disorders research (30 papers), Bone and Dental Protein Studies (14 papers) and Protease and Inhibitor Mechanisms (8 papers). Aileen M. Barnes is often cited by papers focused on Connective tissue disorders research (30 papers), Bone and Dental Protein Studies (14 papers) and Protease and Inhibitor Mechanisms (8 papers). Aileen M. Barnes collaborates with scholars based in United States, Canada and Italy. Aileen M. Barnes's co-authors include Joan C. Marini, Wayne A. Cabral, Antonella Forlino, Weizhong Chang, Elena Makareeva, Sergey Leikin, David R. Eyre, MaryAnn Weis, Katherine Kalil and Erik W. Dent and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Aileen M. Barnes

32 papers receiving 2.5k 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.

New perspectives on osteogenesis imperfecta

2011 497 citations Antonella Forlino, Wayne A. Cabral et al. Nature Reviews Endocrinology profile →

Peers

Aileen M. Barnes

GENET

RHEUM

ONCOL

Wayne A. Cabral United States

Michael D. Briggs United Kingdom

Przemko Tylżanowski Belgium

Lisa Garrett‐Beal United States

Masahiro Iwamoto Japan

Timothy F. Day United States

Janice A. Vranka United States

Elda Munivez United States

Ikuyo Kou Japan

Daniela Später United States

Wayne A. Cabral United States

Aileen M. Barnes

2.1k ×1.2

GENET

1.2k ×1.2

RHEUM

1.0k ×1.3

498 ×1.1

462 ×1.2

ONCOL

Citations per year, relative to Aileen M. Barnes Aileen M. Barnes (= 1×) peers Wayne A. Cabral

Countries citing papers authored by Aileen M. Barnes

Since Specialization

Citations

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

Fields of papers citing papers by Aileen M. Barnes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aileen M. Barnes. 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 Aileen M. Barnes. The network helps show where Aileen M. Barnes may publish in the future.

Co-authorship network of co-authors of Aileen M. Barnes

This figure shows the co-authorship network connecting the top 25 collaborators of Aileen M. Barnes. A scholar is included among the top collaborators of Aileen M. Barnes 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 Aileen M. Barnes. Aileen M. Barnes 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

Besio, Roberta, Raymond Dalgleish, Simona Villani, et al.. (2022). Dissecting the phenotypic variability of osteogenesis imperfecta. Disease Models & Mechanisms. 15(5). 31 indexed citations

El‐Gazzar, Ahmed, Heeseog Kang, Nadja Fratzl‐Zelman, et al.. (2022). SMAD3 mutation in LDS3 causes bone fragility by impairing the TGF-β pathway and enhancing osteoclastogenesis. Bone Reports. 17. 101603–101603. 3 indexed citations

Cabral, Wayne A., Nadja Fratzl‐Zelman, MaryAnn Weis, et al.. (2020). Substitution of murine type I collagen A1 3-hydroxylation site alters matrix structure but does not recapitulate osteogenesis imperfecta bone dysplasia. Matrix Biology. 90. 20–39. 16 indexed citations

Barnes, Aileen M., Aarthi Ashok, Elena Makareeva, et al.. (2019). COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1865(9). 2210–2223. 19 indexed citations

Mumm, Steven, Gary S. Gottesman, Deborah Wenkert, et al.. (2019). Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation. Bone. 130. 115047–115047. 16 indexed citations

Wang, Min, Laurianne Imbert, Aileen M. Barnes, et al.. (2016). Bone mineral properties in growing Col1a2+/G610C mice, an animal model of osteogenesis imperfecta. Bone. 87. 120–129. 31 indexed citations

Cabral, Wayne A., Masaki Ishikawa, Matthias Garten, et al.. (2016). Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta. PLoS Genetics. 12(7). e1006156–e1006156. 49 indexed citations

Symoens, Sofie, Aileen M. Barnes, Charlotte Gistelinck, et al.. (2015). Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia. The American Journal of Human Genetics. 97(4). 521–534. 32 indexed citations

Reich, Adi, Aileen M. Barnes, Wayne A. Cabral, et al.. (2014). Type V OI Primary Osteoblasts Display Increased Mineralization Despite DecreasedCOL1A1Expression. The Journal of Clinical Endocrinology & Metabolism. 100(2). E325–E332. 28 indexed citations

10.

Takagi, Masaki, Tomohiro Ishii, Aileen M. Barnes, et al.. (2012). A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta. PLoS ONE. 7(5). e36809–e36809. 27 indexed citations

11.

Barnes, Aileen M., Wayne A. Cabral, MaryAnn Weis, et al.. (2012). Absence ofFKBP10in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix. Human Mutation. 33(11). 1589–1598. 75 indexed citations

12.

Valli, Maurizia, Aileen M. Barnes, Simona Viglio, et al.. (2011). Deficiency of CRTAP in non‐lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. Clinical Genetics. 82(5). 453–459. 23 indexed citations

13.

Forlino, Antonella, Wayne A. Cabral, Aileen M. Barnes, & Joan C. Marini. (2011). New perspectives on osteogenesis imperfecta. Nature Reviews Endocrinology. 7(9). 540–557. 497 indexed citations breakdown →

14.

Lindahl, Katarina, Aileen M. Barnes, Nadja Fratzl‐Zelman, et al.. (2011). COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta. Human Mutation. 32(6). 598–609. 94 indexed citations

15.

Chang, Weizhong, Aileen M. Barnes, Wayne A. Cabral, Joann Bodurtha, & Joan C. Marini. (2009). Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex. Human Molecular Genetics. 19(2). 223–234. 58 indexed citations

16.

Cabral, Wayne A., Weizhong Chang, Aileen M. Barnes, et al.. (2007). Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta. Nature Genetics. 39(3). 359–365. 317 indexed citations

17.

Makareeva, Elena, Edward L. Mertz, Natalia V. Kuznetsova, et al.. (2007). Structural Heterogeneity of Type I Collagen Triple Helix and Its Role in Osteogenesis Imperfecta. Journal of Biological Chemistry. 283(8). 4787–4798. 75 indexed citations

18.

Marini, Joan C., Wayne A. Cabral, Aileen M. Barnes, & Weizhong Chang. (2007). Components of the Collagen Prolyl 3-Hydroxylation Complex are Crucial for Normal Bone Development. Cell Cycle. 6(14). 1675–1681. 87 indexed citations

19.

Barnes, Aileen M., Weizhong Chang, Roy Morello, et al.. (2006). Deficiency of Cartilage-Associated Protein in Recessive Lethal Osteogenesis Imperfecta. New England Journal of Medicine. 355(26). 2757–2764. 228 indexed citations

20.

Dent, Erik W., et al.. (2004). Netrin-1 and Semaphorin 3A Promote or Inhibit Cortical Axon Branching, Respectively, by Reorganization of the Cytoskeleton. Journal of Neuroscience. 24(12). 3002–3012. 228 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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