Daniela V. Luquetti

1.8k total citations
44 papers, 1.2k citations indexed

About

Daniela V. Luquetti is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Daniela V. Luquetti has authored 44 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 10 papers in Molecular Biology. Recurrent topics in Daniela V. Luquetti's work include Cleft Lip and Palate Research (25 papers), Craniofacial Disorders and Treatments (24 papers) and Prenatal Screening and Diagnostics (9 papers). Daniela V. Luquetti is often cited by papers focused on Cleft Lip and Palate Research (25 papers), Craniofacial Disorders and Treatments (24 papers) and Prenatal Screening and Diagnostics (9 papers). Daniela V. Luquetti collaborates with scholars based in United States, Brazil and Australia. Daniela V. Luquetti's co-authors include Carrie L. Heike, Anne Hing, Timothy C. Cox, Michael L. Cunningham, Pierpaolo Mastroiacovo, Emanuele Leoncini, Craig B. Birgfeld, Babette S. Saltzman, Eric E. Turner and Rosalina Jorge Koifman and has published in prestigious journals such as The Journal of Pediatrics, Plastic & Reconstructive Surgery and Cadernos de Saúde Pública.

In The Last Decade

Daniela V. Luquetti

44 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniela V. Luquetti United States	20	660	660	309	257	144	44	1.2k
Elizabeth J. Leslie United States	20	202 0.3×	1.2k 1.7×	225 0.7×	30 0.1×	40 0.3×	65	1.4k
K.G.H. van der Wal Netherlands	22	558 0.8×	821 1.2×	47 0.2×	95 0.4×	15 0.1×	66	1.6k
R Rullo Italy	20	236 0.4×	326 0.5×	211 0.7×	52 0.2×	14 0.1×	54	1.2k
David A. Staffenberg United States	21	629 1.0×	853 1.3×	32 0.1×	41 0.2×	61 0.4×	85	1.4k
Craig B. Birgfeld United States	21	508 0.8×	868 1.3×	39 0.1×	20 0.1×	82 0.6×	63	1.1k
Figen Özgür Türkiye	16	238 0.4×	331 0.5×	63 0.2×	46 0.2×	16 0.1×	79	968
Piotr Wójcicki Poland	15	224 0.3×	441 0.7×	119 0.4×	42 0.2×	25 0.2×	54	726
Khoo Boo-Chai United Kingdom	17	490 0.7×	390 0.6×	110 0.4×	28 0.1×	24 0.2×	213	1.2k
Dylan J. Murray Ireland	16	435 0.7×	251 0.4×	38 0.1×	65 0.3×	24 0.2×	50	885
Cássio Eduardo Raposo-Amaral Brazil	20	532 0.8×	657 1.0×	100 0.3×	21 0.1×	11 0.1×	112	1.1k

Countries citing papers authored by Daniela V. Luquetti

Since Specialization

Citations

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

Fields of papers citing papers by Daniela V. Luquetti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniela V. Luquetti. 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 Daniela V. Luquetti. The network helps show where Daniela V. Luquetti may publish in the future.

Co-authorship network of co-authors of Daniela V. Luquetti

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela V. Luquetti. A scholar is included among the top collaborators of Daniela V. Luquetti 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 Daniela V. Luquetti. Daniela V. Luquetti 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

Crerand, Canice E., Nicola Marie Stock, Daniela V. Luquetti, et al.. (2020). Microtia and craniofacial microsomia: Content analysis of facebook groups. International Journal of Pediatric Otorhinolaryngology. 138. 110301–110301. 14 indexed citations

Speltz, Matthew L., Kathleen A. Kapp‐Simon, Alexis L. Johns, et al.. (2018). Neurodevelopment of Infants with and without Craniofacial Microsomia. The Journal of Pediatrics. 198. 226–233.e3. 15 indexed citations

Luquetti, Daniela V., et al.. (2018). Healthcare and psychosocial experiences of individuals with craniofacial microsomia: Patient and caregivers perspectives. International Journal of Pediatric Otorhinolaryngology. 107. 164–175. 23 indexed citations

Speltz, Matthew L., Erin R. Wallace, Brent R. Collett, et al.. (2017). Intelligence and Academic Achievement of Adolescents with Craniofacial Microsomia. Plastic & Reconstructive Surgery. 140(3). 571–580. 26 indexed citations

Birgfeld, Craig B., Carrie L. Heike, Babette S. Saltzman, et al.. (2016). Reliable classification of facial phenotypic variation in craniofacial microsomia: a comparison of physical exam and photographs. Head & Face Medicine. 12(1). 14–14. 23 indexed citations

Saltzman, Babette S., et al.. (2016). Phenotypic characterization of epibulbar dermoids. International Ophthalmology. 37(3). 499–505. 4 indexed citations

Heike, Carrie L., Daniela V. Luquetti, & Anne Hing. (2014). Craniofacial Microsomia Overview. 33 indexed citations

Cox, Timothy C., et al.. (2014). The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research. European Journal of Medical Genetics. 57(8). 394–401. 69 indexed citations

Cox, Timothy C., Daniela V. Luquetti, & Michael L. Cunningham. (2013). Perspectives and challenges in advancing research into craniofacial anomalies. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 163(4). 213–217. 9 indexed citations

10.

Luquetti, Daniela V., Babette S. Saltzman, Kathleen C.Y. Sie, et al.. (2013). Interrater reliability of a phenotypic assessment tool for the ear morphology in microtia. American Journal of Medical Genetics Part A. 161(6). 1264–1272. 10 indexed citations

11.

Luquetti, Daniela V., Babette S. Saltzman, Luiz André Freire Pimenta, et al.. (2012). Evaluation of ICD‐9‐CM codes for craniofacial microsomia. Birth Defects Research Part A Clinical and Molecular Teratology. 94(12). 990–995. 8 indexed citations

12.

Luquetti, Daniela V., Anne Hing, Mark J. Rieder, et al.. (2012). “Mandibulofacial dysostosis with microcephaly” caused by EFTUD2 mutations: Expanding the phenotype. American Journal of Medical Genetics Part A. 161(1). 108–113. 55 indexed citations

13.

Quina, Lely A., Takashi Kuramoto, Daniela V. Luquetti, et al.. (2012). Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a novel cause of congenital ear malformation. Disease Models & Mechanisms. 5(6). 812–22. 20 indexed citations

14.

Luquetti, Daniela V., Carrie L. Heike, Anne Hing, Michael L. Cunningham, & Timothy C. Cox. (2011). Microtia: Epidemiology and genetics. American Journal of Medical Genetics Part A. 158A(1). 124–139. 305 indexed citations

15.

Luquetti, Daniela V., Emanuele Leoncini, & Pierpaolo Mastroiacovo. (2011). Microtia‐anotia: A global review of prevalence rates. Birth Defects Research Part A Clinical and Molecular Teratology. 91(9). 813–822. 153 indexed citations

16.

Luquetti, Daniela V. & Rosalina Jorge Koifman. (2010). Qualidade da notificação de anomalias congênitas pelo Sistema de Informações sobre Nascidos Vivos (SINASC): estudo comparativo nos anos 2004 e 2007. Cadernos de Saúde Pública. 26(9). 1756–1765. 21 indexed citations

17.

Monica, Matteo Della, Fortunato Lonardo, Francesca Faravelli, et al.. (2007). A case of autism with an interstitial 1q deletion (1q23.3‐24.2) and a de novo translocation of chromosomes 1q and 5q. American Journal of Medical Genetics Part A. 143A(22). 2733–2737. 12 indexed citations

18.

Luquetti, Daniela V., et al.. (2007). Gillespie Syndrome: Additional Findings and Parental Consanguinity. Ophthalmic Genetics. 28(2). 89–93. 7 indexed citations

19.

Lonardo, Fortunato, et al.. (2007). Al‐Awadi/Raas‐Rothschild syndrome: Two new cases and review. American Journal of Medical Genetics Part A. 143A(24). 3169–3174. 4 indexed citations

20.

Cavalcanti, Denise P., et al.. (2006). Fraser and Ablepharon macrostomia phenotypes: Concurrence in one family and association with mutatedFRAS1. American Journal of Medical Genetics Part A. 143A(3). 241–247. 17 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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