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
Comparison fields: 5 of 126
  • Genetics 1.9k
  • Molecular Biology 1.0k
  • Pulmonary and Respiratory Medicine 690
  • Rheumatology 561
  • Orthopedics and Sports Medicine 556
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 View profile →
Citations per field, relative to Marcia Willing
Marcia Willing · 1×
Citations per year, relative to Marcia Willing
Marcia Willing · 1×

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

20 of 20 papers shown
# Title Journal Authors Indexed citations
1 Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses American Journal of Medical Genetics Part A Jorge L. Granadillo, Daniel Wegner et al. 9
2 Ectopia lentis in Loeys‐Dietz syndrome type 4 American Journal of Medical Genetics Part A Alan C. Braverman, Kevin J. Blinder et al. 5
3 Pregnancy after aortic root replacement in Loeys–Dietz syndrome: High risk of aortic dissection American Journal of Medical Genetics Part A Alan C. Braverman, Marc R. Moon et al. 20
4 Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis Journal of Bone and Joint Surgery Gabe Haller, David M. Alvarado et al. 5
5 Effects of enamel matrix genes on dental caries are moderated by fluoride exposures Human Genetics John R. Shaffer, Jenna C. Carlson et al. 31
6 A Hip Analysis Protocol for Pediatric Bone Densitometry: The Iowa Bone Development Study Journal of Clinical Densitometry Julie M. Eichenberger Gilmore, Trudy L. Burns et al. 3
7 TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections Cardiovascular Research Sakiko Inamoto, Callie Kwartler et al. 97
8 Associations of fluoride intake with children’s bone measures at age 11 Community Dentistry And Oral Epidemiology Steven M. Levy, Julie M. Eichenberger‐Gilmore et al. 16
9 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 Kathleen F. Janz, Elena M. Letuchy et al. 29
10 Physical activity augments bone mineral accrual in young children: The Iowa Bone Development Study The Journal of Pediatrics Kathleen F. Janz, Julie M. Eichenberger Gilmore et al. 73
11 Everyday Activity Predicts Bone Geometry in Children: The Iowa Bone Development Study Medicine & Science in Sports & Exercise Kathleen F. Janz, Trudy L. Burns et al. 90
12 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 Lary C. Walker, Marcia Willing et al. 16
13 Estrogen Receptor Genotypes and Their Association with the 10-Year Changes in Bone Mineral Density and Osteocalcin Concentrations The Journal of Clinical Endocrinology & Metabolism MaryFran Sowers, Mary Jannausch et al. 17
14 COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS The American Journal of Human Genetics Richard Wenstrup, Jane B. Florer et al. 91
15 Osteocalcin: Genetic and Physical Mapping of the Human Gene BGLAP and Its Potential Role in Postmenopausal Osteoporosis Genomics Michael H. Raymond, Brian C. Schutte et al. 43
16 Molecular heterogeneity in osteogenesis imperfecta type I American Journal of Medical Genetics Marcia Willing, Charles J. Pruchno et al. 21
17 Osteogenesis imperfecta: translation of mutation to phenotype. Journal of Medical Genetics Peter H. Byers, Gillian A. Wallis et al. 238
18 Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagen Human Genetics Charles J. Pruchno, Daniel H. Cohn et al. 29
19 Osteogenesis Imperfecta: The Molecular Basis of Clinical Heterogeneitya Annals of the New York Academy of Sciences Peter H. Byers, Jeffrey Bonadio et al. 32
20 Regulation of human globin gene expression in mouse erythroleukemia � human fibroblast hybrid cells Somatic Cell and Molecular Genetics Neal S. Young, Marcia Willing et al. 7

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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