Peggy Modaff

1.0k total citations
35 papers, 625 citations indexed

About

Peggy Modaff is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Peggy Modaff has authored 35 papers receiving a total of 625 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 13 papers in Pulmonary and Respiratory Medicine and 10 papers in Molecular Biology. Recurrent topics in Peggy Modaff's work include Connective tissue disorders research (17 papers), Neonatal Respiratory Health Research (9 papers) and Family and Disability Support Research (3 papers). Peggy Modaff is often cited by papers focused on Connective tissue disorders research (17 papers), Neonatal Respiratory Health Research (9 papers) and Family and Disability Support Research (3 papers). Peggy Modaff collaborates with scholars based in United States, South Korea and Netherlands. Peggy Modaff's co-authors include Richard M. Pauli, Amy White, Janet M. Legare, Julie Hoover‐Fong, Susan L. Sipes, Michael P. Whyte, Michael B. Bober, S. Shahrukh Hashmi, Jacqueline T. Hecht and V. Kim Horton and has published in prestigious journals such as The American Journal of Human Genetics, The Laryngoscope and Human Mutation.

In The Last Decade

Peggy Modaff

34 papers receiving 601 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peggy Modaff United States 15 297 229 150 108 86 35 625
Virginia Fano Argentina 15 395 1.3× 206 0.9× 93 0.6× 123 1.1× 83 1.0× 55 634
Vincenzo Antona Italy 19 307 1.0× 428 1.9× 130 0.9× 145 1.3× 117 1.4× 57 821
Vickie Hannig United States 12 185 0.6× 175 0.8× 103 0.7× 83 0.8× 34 0.4× 19 494
Felicity Collins Australia 16 326 1.1× 406 1.8× 155 1.0× 133 1.2× 23 0.3× 22 760
Daniele Tessaris Italy 15 137 0.5× 184 0.8× 127 0.8× 37 0.3× 68 0.8× 37 515
Anna Elsa Maria Allegri Italy 18 161 0.5× 285 1.2× 211 1.4× 86 0.8× 131 1.5× 43 830
G. Fekete Hungary 12 173 0.6× 281 1.2× 48 0.3× 75 0.7× 39 0.5× 32 490
Wilhelmina S. Kerstjens‐Frederikse Netherlands 21 402 1.4× 557 2.4× 401 2.7× 258 2.4× 196 2.3× 50 1.4k
Ryszard Ślężak Poland 13 129 0.4× 155 0.7× 35 0.2× 57 0.5× 62 0.7× 50 472
Boris Utsch Germany 20 391 1.3× 596 2.6× 80 0.5× 224 2.1× 136 1.6× 32 951

Countries citing papers authored by Peggy Modaff

Since Specialization
Citations

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

Fields of papers citing papers by Peggy Modaff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peggy Modaff

This figure shows the co-authorship network connecting the top 25 collaborators of Peggy Modaff. A scholar is included among the top collaborators of Peggy Modaff 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 Peggy Modaff. Peggy Modaff 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.
Legare, Janet M., David G. Ingram, Richard M. Pauli, et al.. (2025). Evolution of sleep disordered breathing in infants with achondroplasia. Sleep And Breathing. 29(1). 88–88.
2.
Nahm, Nickolas J., William G. Mackenzie, William G. Mackenzie, et al.. (2023). Achondroplasia natural history study (CLARITY): 60-year experience in orthopedic surgery from four skeletal dysplasia centers. Orphanet Journal of Rare Diseases. 18(1). 139–139. 10 indexed citations
3.
Paloian, Neil J., et al.. (2022). Real-world effectiveness of burosumab in children with X-linked hypophosphatemic rickets. Pediatric Nephrology. 37(11). 2667–2677. 14 indexed citations
4.
Hoover‐Fong, Julie, S. Shahrukh Hashmi, Jacqueline T. Hecht, et al.. (2021). Achondroplasia Natural History Study (CLARITY): a multicenter retrospective cohort study of achondroplasia in the United States. Genetics in Medicine. 23(8). 1498–1505. 36 indexed citations
5.
Hoover‐Fong, Julie, Kerry Schulze, Michael B. Bober, et al.. (2021). Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study—a multi-center retrospective cohort study of achondroplasia in the US. Orphanet Journal of Rare Diseases. 16(1). 522–522. 33 indexed citations
6.
Legare, Janet M., et al.. (2020). Apparently benign craniocervical signs in achondroplasia: “neurologic leftovers” identified through a retrospective dataset. Orphanet Journal of Rare Diseases. 15(1). 301–301. 7 indexed citations
7.
Legare, Janet M., et al.. (2020). Craniocervical junction issues after infancy in achondroplasia. American Journal of Medical Genetics Part A. 185(1). 182–189. 5 indexed citations
8.
9.
Legare, Janet M., Peggy Modaff, Bermans J. Iskandar, & Richard M. Pauli. (2016). Syringomyelia in hereditary multiple exostosis. American Journal of Medical Genetics Part A. 170(11). 2956–2959. 1 indexed citations
10.
Jurgens, Julie A., Nara Sobreira, Peggy Modaff, et al.. (2015). NovelCOL2A1Variant (c.619G>A, p.Gly207Arg) Manifesting as a Phenotype Similar to Progressive Pseudorheumatoid Dysplasia and Spondyloepiphyseal Dysplasia, Stanescu Type. Human Mutation. 36(10). 1004–1008. 14 indexed citations
11.
Sobreira, Nara, Peggy Modaff, Gary Steel, et al.. (2014). An anadysplasia‐like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: Further definition of the phenotypic heterogeneity of LBR‐bone dysplasias. American Journal of Medical Genetics Part A. 167(1). 159–163. 11 indexed citations
12.
Modaff, Peggy, et al.. (2013). Airway malacia in children with achondroplasia. American Journal of Medical Genetics Part A. 164(2). 407–414. 15 indexed citations
13.
Dwyer, Ellen, James Hyland, Peggy Modaff, & Richard M. Pauli. (2010). Genotype–phenotype correlation in DTDST dysplasias: Atelosteogenesis type II and diastrophic dysplasia variant in one family. American Journal of Medical Genetics Part A. 152A(12). 3043–3050. 17 indexed citations
14.
Raca, Gordana, et al.. (2009). Array‐based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth. American Journal of Medical Genetics Part A. 149A(11). 2437–2443. 40 indexed citations
15.
Lachman, Ralph, et al.. (2008). A phenotype intermediate between Desbuquois dysplasia and diastrophic dysplasia secondary to mutations in DTDST. American Journal of Medical Genetics Part A. 146A(22). 2920–2924. 9 indexed citations
16.
White, Amy, et al.. (2003). Natural history of rhizomelic chondrodysplasia punctata. American Journal of Medical Genetics Part A. 118A(4). 332–342. 83 indexed citations
17.
Reynolds, Kara, Peggy Modaff, & Richard M. Pauli. (2001). Absence of correlation between infantile hypotonia and foramen magnum size in achondroplasia. American Journal of Medical Genetics. 101(1). 40–45. 17 indexed citations
18.
Pauli, Richard M. & Peggy Modaff. (1999). Jugular bulb dehiscence in achondroplasia. International Journal of Pediatric Otorhinolaryngology. 48(2). 169–174. 7 indexed citations
19.
Pauli, Richard M., Peggy Modaff, Susan L. Sipes, & Michael P. Whyte. (1999). Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: Bent but not broken. American Journal of Medical Genetics. 86(5). 434–438. 50 indexed citations
20.
Modaff, Peggy, V. Kim Horton, & Richard M. Pauli. (1996). ERRORS IN THE PRENATAL DIAGNOSIS OF CHILDREN WITH ACHONDROPLASIA. Prenatal Diagnosis. 16(6). 525–530. 24 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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