Marcia Willing

8.4k total citations
68 papers, 3.7k citations indexed

About

Marcia Willing is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Marcia Willing has authored 68 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Genetics, 21 papers in Molecular Biology and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Marcia Willing's work include Connective tissue disorders research (30 papers), Bone health and osteoporosis research (12 papers) and Aortic Disease and Treatment Approaches (10 papers). Marcia Willing is often cited by papers focused on Connective tissue disorders research (30 papers), Bone health and osteoporosis research (12 papers) and Aortic Disease and Treatment Approaches (10 papers). Marcia Willing collaborates with scholars based in United States, United Kingdom and Canada. Marcia Willing's co-authors include Peter H. Byers, Trudy L. Burns, Steven M. Levy, James C. Torner, Kathleen F. Janz, Gillian A. Wallis, Sachi P. Deschenes, Julie M. Eichenberger Gilmore, Dianna M. Milewicz and Rebecca L. Slayton and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Circulation.

In The Last Decade

Marcia Willing

68 papers receiving 3.6k citations

Peers

Marcia Willing

GENET

PRM

RHEUM

OSM

Silvano Bertelloni Italy

Ravi Savarirayan Australia

Hirotaka Kawano Japan

Oliver Semler Germany

Minna Männikkö Finland

Luca Sangiorgi Italy

Richard M. Pauli United States

Fransiska Malfait Belgium

Pierre B. Saadeh United States

Natsuo Yasui Japan

Silvano Bertelloni Italy

Marcia Willing

1.2k ×0.6

GENET

1.5k ×1.5

273 ×0.4

PRM

362 ×0.6

RHEUM

845 ×1.5

OSM

Citations per year, relative to Marcia Willing Marcia Willing (= 1×) peers Silvano Bertelloni

Countries citing papers authored by Marcia Willing

Since Specialization

Citations

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

Fields of papers citing papers by Marcia Willing

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcia Willing

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

Granadillo, Jorge L., Daniel Wegner, Marcia Willing, et al.. (2020). Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses. American Journal of Medical Genetics Part A. 185(2). 544–548. 9 indexed citations

Braverman, Alan C., Kevin J. Blinder, Sangeeta Khanna, & Marcia Willing. (2020). Ectopia lentis in Loeys‐Dietz syndrome type 4. American Journal of Medical Genetics Part A. 182(8). 1957–1959. 5 indexed citations

Braverman, Alan C., et al.. (2016). Pregnancy after aortic root replacement in Loeys–Dietz syndrome: High risk of aortic dissection. American Journal of Medical Genetics Part A. 170(8). 2177–2180. 20 indexed citations

Haller, Gabe, David M. Alvarado, Marcia Willing, et al.. (2015). Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis. Journal of Bone and Joint Surgery. 97(17). 1411–1417. 5 indexed citations

Shaffer, John R., Jenna C. Carlson, Eleanor Feingold, et al.. (2014). Effects of enamel matrix genes on dental caries are moderated by fluoride exposures. Human Genetics. 134(2). 159–167. 31 indexed citations

Gilmore, Julie M. Eichenberger, Trudy L. Burns, James C. Torner, et al.. (2010). A Hip Analysis Protocol for Pediatric Bone Densitometry: The Iowa Bone Development Study. Journal of Clinical Densitometry. 13(4). 361–369. 3 indexed citations

Inamoto, Sakiko, Callie Kwartler, Andrea L. Lafont, et al.. (2010). TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections. Cardiovascular Research. 88(3). 520–529. 97 indexed citations

Levy, Steven M., Julie M. Eichenberger‐Gilmore, John J. Warren, et al.. (2009). Associations of fluoride intake with children’s bone measures at age 11. Community Dentistry And Oral Epidemiology. 37(5). 416–426. 16 indexed citations

Janz, Kathleen F., Elena M. Letuchy, Trudy L. Burns, et al.. (2008). Subjective and objective measures of physical activity in relationship to bone mineral content during late childhood: the Iowa Bone Development Study. British Journal of Sports Medicine. 42(8). 658–663. 29 indexed citations

10.

Janz, Kathleen F., Julie M. Eichenberger Gilmore, Trudy L. Burns, et al.. (2006). Physical activity augments bone mineral accrual in young children: The Iowa Bone Development Study. The Journal of Pediatrics. 148(6). 793–799. 73 indexed citations

11.

Janz, Kathleen F., Trudy L. Burns, Steven M. Levy, et al.. (2004). Everyday Activity Predicts Bone Geometry in Children: The Iowa Bone Development Study. Medicine & Science in Sports & Exercise. 36(7). 1124–1131. 90 indexed citations

12.

Walker, Lary C., Marcia Willing, Joan C. Marini, et al.. (2004). Heterogeneous basis of the type VIB form of Ehlers–Danlos syndrome (EDS VIB) that is unrelated to decreased collagen lysyl hydroxylation. American Journal of Medical Genetics Part A. 131A(2). 155–162. 16 indexed citations

13.

Sowers, MaryFran, Mary Jannausch, Wei Liang, & Marcia Willing. (2004). Estrogen Receptor Genotypes and Their Association with the 10-Year Changes in Bone Mineral Density and Osteocalcin Concentrations. The Journal of Clinical Endocrinology & Metabolism. 89(2). 733–739. 17 indexed citations

14.

Wenstrup, Richard, Jane B. Florer, Marcia Willing, et al.. (2000). COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS. The American Journal of Human Genetics. 66(6). 1766–1776. 91 indexed citations

15.

Raymond, Michael H., Brian C. Schutte, James C. Torner, Trudy L. Burns, & Marcia Willing. (1999). Osteocalcin: Genetic and Physical Mapping of the Human Gene BGLAP and Its Potential Role in Postmenopausal Osteoporosis. Genomics. 60(2). 210–217. 43 indexed citations

16.

Willing, Marcia, Charles J. Pruchno, & Peter H. Byers. (1993). Molecular heterogeneity in osteogenesis imperfecta type I. American Journal of Medical Genetics. 45(2). 223–227. 21 indexed citations

17.

Byers, Peter H., Gillian A. Wallis, & Marcia Willing. (1991). Osteogenesis imperfecta: translation of mutation to phenotype.. Journal of Medical Genetics. 28(7). 433–442. 238 indexed citations

18.

Pruchno, Charles J., Daniel H. Cohn, Gillian A. Wallis, et al.. (1991). Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagen. Human Genetics. 87(1). 33–40. 29 indexed citations

19.

Byers, Peter H., Jeffrey Bonadio, Daniel H. Cohn, et al.. (1988). Osteogenesis Imperfecta: The Molecular Basis of Clinical Heterogeneity^a. Annals of the New York Academy of Sciences. 543(1). 117–128. 32 indexed citations

20.

Young, Neal S., et al.. (1982). Regulation of human globin gene expression in mouse erythroleukemia � human fibroblast hybrid cells. Somatic Cell and Molecular Genetics. 8(2). 163–178. 7 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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