MaryAnn Weis

3.8k total citations
40 papers, 2.4k citations indexed

About

MaryAnn Weis is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, MaryAnn Weis has authored 40 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 16 papers in Molecular Biology and 13 papers in Oncology. Recurrent topics in MaryAnn Weis's work include Connective tissue disorders research (33 papers), Bone and Dental Protein Studies (9 papers) and Bone health and treatments (8 papers). MaryAnn Weis is often cited by papers focused on Connective tissue disorders research (33 papers), Bone and Dental Protein Studies (9 papers) and Bone health and treatments (8 papers). MaryAnn Weis collaborates with scholars based in United States, United Kingdom and Canada. MaryAnn Weis's co-authors include David R. Eyre, Aileen M. Barnes, Joan C. Marini, Wayne A. Cabral, Elena Makareeva, Sergey Leikin, Weizhong Chang, Jyoti Rai, Natalia V. Kuznetsova and Brendan Lee and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

MaryAnn Weis

38 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
MaryAnn Weis United States	24	1.3k	998	748	407	321	40	2.4k
Elena Makareeva United States	23	1.3k 1.0×	721 0.7×	716 1.0×	417 1.0×	340 1.1×	40	2.0k
Wayne A. Cabral United States	29	2.1k 1.6×	1.0k 1.0×	1.2k 1.6×	498 1.2×	462 1.4×	55	3.0k
Mary Ann Weis United States	27	1.0k 0.8×	894 0.9×	863 1.2×	318 0.8×	491 1.5×	38	2.6k
Cecilia Giunta Switzerland	28	1.5k 1.2×	805 0.8×	581 0.8×	218 0.5×	320 1.0×	69	2.4k
Shireen R. Lamandé Australia	30	902 0.7×	1.6k 1.6×	534 0.7×	344 0.8×	169 0.5×	84	3.0k
Michael D. Briggs United Kingdom	35	1.3k 1.0×	1.6k 1.6×	1.3k 1.8×	396 1.0×	312 1.0×	75	3.4k
Masahiro Iwamoto Japan	27	584 0.4×	1.9k 1.9×	1.1k 1.5×	364 0.9×	419 1.3×	57	2.9k
Tatsuya Furuichi Japan	23	482 0.4×	2.1k 2.1×	695 0.9×	558 1.4×	676 2.1×	40	3.2k
Rosa Serra United States	40	1.6k 1.2×	3.4k 3.4×	980 1.3×	415 1.0×	758 2.4×	88	5.2k
Víctor L. Ruiz‐Pérez Spain	30	2.1k 1.5×	2.4k 2.4×	431 0.6×	291 0.7×	433 1.3×	52	3.5k

Countries citing papers authored by MaryAnn Weis

Since Specialization

Citations

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

Fields of papers citing papers by MaryAnn Weis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of MaryAnn Weis

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

Lim, Joohyun, Caressa Lietman, Matthew W. Grol, et al.. (2021). Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta. Proceedings of the National Academy of Sciences. 118(25). 7 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

Stegen, Steve, Kjell Laperre, Guy Eelen, et al.. (2019). HIF-1α metabolically controls collagen synthesis and modification in chondrocytes. Nature. 565(7740). 511–515. 233 indexed citations

Gistelinck, Charlotte, Ronald Y. Kwon, Fransiska Malfait, et al.. (2018). Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies. Proceedings of the National Academy of Sciences. 115(34). E8037–E8046. 69 indexed citations

Hudson, David M., MaryAnn Weis, Jyoti Rai, et al.. (2017). P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA. Journal of Biological Chemistry. 292(9). 3877–3887. 29 indexed citations

Hudson, David M., Kyu Sang Joeng, Abbhirami Rajagopal, et al.. (2015). Post-translationally Abnormal Collagens of Prolyl 3-Hydroxylase-2 Null Mice Offer a Pathobiological Mechanism for the High Myopia Linked to Human LEPREL1 Mutations. Journal of Biological Chemistry. 290(13). 8613–8622. 36 indexed citations

Lietman, Caressa, Abbhirami Rajagopal, Erica P. Homan, et al.. (2014). Connective tissue alterations in Fkbp10−/− mice. Human Molecular Genetics. 23(18). 4822–4831. 48 indexed citations

Durán, Iván, Lisette Nevarez, Pavel Krejčı́, et al.. (2014). HSP47 and FKBP65 cooperate in the synthesis of type I procollagen. Human Molecular Genetics. 24(7). 1918–1928. 45 indexed citations

10.

Hudson, David M., et al.. (2014). Evolutionary Origins of C-Terminal (GPP)n 3-Hydroxyproline Formation in Vertebrate Tendon Collagen. PLoS ONE. 9(4). e93467–e93467. 18 indexed citations

11.

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

12.

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

13.

Krejčı́, Pavel, Markéta Kaucká, Jiřina Procházková, et al.. (2012). Receptor Tyrosine Kinases Activate Canonical WNT/β-Catenin Signaling via MAP Kinase/LRP6 Pathway and Direct β-Catenin Phosphorylation. PLoS ONE. 7(4). e35826–e35826. 132 indexed citations

14.

Hudson, David M., MaryAnn Weis, & David R. Eyre. (2011). Insights on the Evolution of Prolyl 3-Hydroxylation Sites from Comparative Analysis of Chicken and Xenopus Fibrillar Collagens. PLoS ONE. 6(5). e19336–e19336. 13 indexed citations

15.

Baldridge, Dustin, Jennifer Lennington, MaryAnn Weis, et al.. (2010). Generalized Connective Tissue Disease in Crtap-/- Mouse. PLoS ONE. 5(5). e10560–e10560. 46 indexed citations

16.

Giunta, Cecilia, Nursel Elçioğlu, Beate Albrecht, et al.. (2008). Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13. The American Journal of Human Genetics. 82(6). 1290–1305. 149 indexed citations

17.

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

18.

Fernandes, Russell J., MaryAnn Weis, Melissa A. Scott, Robert E. Seegmiller, & David R. Eyre. (2007). Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse. Matrix Biology. 26(8). 597–603. 43 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.

Weis, MaryAnn. (2004). Inhibiting long chain fatty Acyl CoA synthetase increases basal and agonist-stimulated NO synthesis in endothelium*1. Cardiovascular Research. 63(2). 338–346. 13 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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