Mary Ann Weis

3.6k total citations · 1 hit paper
38 papers, 2.6k citations indexed

About

Mary Ann Weis is a scholar working on Rheumatology, Genetics and Immunology and Allergy. According to data from OpenAlex, Mary Ann Weis has authored 38 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Rheumatology, 20 papers in Genetics and 13 papers in Immunology and Allergy. Recurrent topics in Mary Ann Weis's work include Connective tissue disorders research (19 papers), Osteoarthritis Treatment and Mechanisms (13 papers) and Cell Adhesion Molecules Research (13 papers). Mary Ann Weis is often cited by papers focused on Connective tissue disorders research (19 papers), Osteoarthritis Treatment and Mechanisms (13 papers) and Cell Adhesion Molecules Research (13 papers). Mary Ann Weis collaborates with scholars based in United States, Sweden and Germany. Mary Ann Weis's co-authors include David R. Eyre, Jiann-Jiu Wu, David W. Eyre, S Maslan, Anne‐Marie Bollen, Frederick R. Singer, Dennis A. Hanson, Terri Pietka, Peter H. Byers and Russell J. Fernandes and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Mary Ann Weis

37 papers receiving 2.5k citations

Hit Papers

A specific immunoassay fo... 1992 2026 2003 2014 1992 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mary Ann Weis United States 27 1.0k 894 863 491 482 38 2.6k
MaryAnn Weis United States 24 1.3k 1.3× 998 1.1× 748 0.9× 321 0.7× 234 0.5× 40 2.4k
Su‐Li Cheng United States 32 732 0.7× 2.4k 2.6× 635 0.7× 682 1.4× 351 0.7× 53 4.4k
Eric Haÿ France 32 455 0.5× 1.7k 1.9× 755 0.9× 578 1.2× 246 0.5× 66 3.0k
Roy Morello United States 26 1.4k 1.4× 1.1k 1.3× 822 1.0× 338 0.7× 179 0.4× 52 2.7k
Charlotte L. Phillips United States 26 824 0.8× 573 0.6× 415 0.5× 181 0.4× 242 0.5× 67 2.1k
Jürgen Brinckmann Germany 27 647 0.6× 922 1.0× 347 0.4× 246 0.5× 127 0.3× 65 2.8k
Dominique Modrowski France 32 394 0.4× 1.4k 1.6× 408 0.5× 616 1.3× 603 1.3× 59 2.9k
Leonard Rifas United States 27 480 0.5× 1.7k 1.9× 630 0.7× 941 1.9× 562 1.2× 49 3.5k
Philip Osdoby United States 35 533 0.5× 2.3k 2.6× 703 0.8× 1.4k 2.9× 652 1.4× 66 3.8k
S.Y. Ali United Kingdom 30 383 0.4× 768 0.9× 1.5k 1.7× 300 0.6× 348 0.7× 75 2.7k

Countries citing papers authored by Mary Ann Weis

Since Specialization
Citations

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

Fields of papers citing papers by Mary Ann Weis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary Ann Weis. 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 Mary Ann Weis. The network helps show where Mary Ann Weis may publish in the future.

Co-authorship network of co-authors of Mary Ann Weis

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

All Works

20 of 20 papers shown
1.
Grigelioniené, Giedré, Hiroshi Suzuki, Fulya Taylan, et al.. (2019). Gain-of-function mutation of microRNA-140 in human skeletal dysplasia. Nature Medicine. 25(4). 583–590. 70 indexed citations
2.
Durán, Iván, Jorge Martı́n, Mary Ann Weis, et al.. (2017). A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen. Journal of Bone and Mineral Research. 32(6). 1309–1319. 56 indexed citations
3.
Lindert, Uschi, Mary Ann Weis, Jyoti Rai, et al.. (2015). Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta. Journal of Biological Chemistry. 290(29). 17679–17689. 36 indexed citations
4.
Lietman, Caressa, Ronit Marom, Elda Munivez, et al.. (2014). A Transgenic Mouse Model of OI Type V Supports a Neomorphic Mechanism of the IFITM5 Mutation. Journal of Bone and Mineral Research. 30(3). 489–498. 29 indexed citations
5.
McAlinden, Audrey, Uwe Hansen, Mary Ann Weis, et al.. (2013). Molecular properties and fibril ultrastructure of types II and XI collagens in cartilage of mice expressing exclusively the α1(IIA) collagen isoform. Matrix Biology. 34. 105–113. 24 indexed citations
6.
7.
Fernandes, Russell J., et al.. (2011). A Role for Prolyl 3-Hydroxylase 2 in Post-translational Modification of Fibril-forming Collagens. Journal of Biological Chemistry. 286(35). 30662–30669. 35 indexed citations
8.
Christiansen, Helena E., Ulrike Schwarze, Shawna M. Pyott, et al.. (2010). Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 86(3). 389–398. 228 indexed citations
9.
Wu, Jiann-Jiu, et al.. (2010). Type III Collagen, a Fibril Network Modifier in Articular Cartilage. Journal of Biological Chemistry. 285(24). 18537–18544. 77 indexed citations
10.
Eyre, David R., et al.. (2010). Maturation of Collagen Ketoimine Cross-links by an Alternative Mechanism to Pyridinoline Formation in Cartilage. Journal of Biological Chemistry. 285(22). 16675–16682. 34 indexed citations
11.
Weis, Mary Ann, et al.. (2009). Location of 3-Hydroxyproline Residues in Collagen Types I, II, III, and V/XI Implies a Role in Fibril Supramolecular Assembly. Journal of Biological Chemistry. 285(4). 2580–2590. 129 indexed citations
12.
Eyre, David R., Mary Ann Weis, & Jiann-Jiu Wu. (2008). Advances in collagen cross-link analysis. Methods. 45(1). 65–74. 165 indexed citations
13.
Shapiro, Frederic, Howard Mulhern, Mary Ann Weis, & David R. Eyre. (2006). Rough Endoplasmic Reticulum Abnormalities in a Patient with Spondyloepimetaphyseal Dysplasia with Scoliosis, Joint Laxity, and Finger Deformities. Ultrastructural Pathology. 30(5). 393–400. 4 indexed citations
14.
Matsui, Yoshito, Jiann-Jiu Wu, Mary Ann Weis, Terri Pietka, & David R. Eyre. (2003). Matrix deposition of tryptophan-containing allelic variants of type IX collagen in developing human cartilage. Matrix Biology. 22(2). 123–129. 18 indexed citations
15.
Eyre, David R., Jiann-Jiu Wu, Russell J. Fernandes, Terri Pietka, & Mary Ann Weis. (2002). Recent developments in cartilage research: matrix biology of the collagen II/IX/XI heterofibril network. Biochemical Society Transactions. 30(6). 894–900. 14 indexed citations
16.
Eyre, David R., Jiann-Jiu Wu, Russell J. Fernandes, Terri Pietka, & Mary Ann Weis. (2001). Recent developments in cartilage research: matrix biology of the collagen II/IX/XI heterofibril network. Biochemical Society Transactions. 30(6). 893–893. 69 indexed citations
17.
Fernandes, Russell J., Douglas J. Wilkin, Mary Ann Weis, et al.. (1998). Incorporation of Structurally Defective Type II Collagen into Cartilage Matrix in Kniest Chondrodysplasia. Archives of Biochemistry and Biophysics. 355(2). 282–290. 28 indexed citations
18.
Tiller, George E., Mary Ann Weis, Ralph S. Lachman, et al.. (1995). Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick type. Nature Genetics. 11(1). 87–89. 61 indexed citations
19.
Eyre, David R., Mary Ann Weis, & R. W. Moskowitz. (1991). Cartilage expression of a type II collagen mutation in an inherited form of osteoarthritis associated with a mild chondrodysplasia.. Journal of Clinical Investigation. 87(1). 357–361. 61 indexed citations
20.
Starman, B J, David R. Eyre, Harry Charbonneau, et al.. (1989). Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotype.. Journal of Clinical Investigation. 84(4). 1206–1214. 67 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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