Nada Quercia

1.1k total citations
17 papers, 256 citations indexed

About

Nada Quercia is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nada Quercia has authored 17 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nada Quercia's work include Hearing, Cochlea, Tinnitus, Genetics (2 papers), BRCA gene mutations in cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Nada Quercia is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (2 papers), BRCA gene mutations in cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Nada Quercia collaborates with scholars based in Canada, United States and Australia. Nada Quercia's co-authors include Sharon Dell, Nisreen Rumman, Raymond H. Kim, T H Kirkham, Katherine Fu, Eric A. Shoubridge, David H. Zackon, David Chitayat, E. Andermann and Carol Macmillan and has published in prestigious journals such as Neurology, The Laryngoscope and Journal of Medical Genetics.

In The Last Decade

Nada Quercia

16 papers receiving 250 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nada Quercia Canada	8	148	95	39	31	28	17	256
Maria Grazia Patricelli Italy	10	176 1.2×	185 1.9×	16 0.4×	5 0.2×	49 1.8×	21	322
Rachel Slaugh United States	7	227 1.5×	104 1.1×	64 1.6×	41 1.3×	24 0.9×	11	307
Naomi Meeks United States	8	86 0.6×	50 0.5×	7 0.2×	64 2.1×	36 1.3×	16	169
Xena Giada Pappalardo Italy	8	170 1.1×	58 0.6×	12 0.3×	25 0.8×	28 1.0×	32	263
Christian Wentzel Sweden	7	196 1.3×	188 2.0×	28 0.7×	10 0.3×	112 4.0×	8	373
Paula Grigorescu‐Sido Romania	9	138 0.9×	81 0.9×	15 0.4×	12 0.4×	13 0.5×	33	310
Márta Czakó Hungary	11	112 0.8×	141 1.5×	25 0.6×	5 0.2×	30 1.1×	40	245
Ann Seman United States	5	97 0.7×	41 0.4×	15 0.4×	6 0.2×	18 0.6×	5	215
Boris Zagradišnik Slovenia	10	113 0.8×	131 1.4×	12 0.3×	6 0.2×	55 2.0×	28	263
F Pascu Germany	6	213 1.4×	125 1.3×	20 0.5×	117 3.8×	81 2.9×	7	412

Countries citing papers authored by Nada Quercia

Since Specialization

Citations

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

Fields of papers citing papers by Nada Quercia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nada Quercia

This figure shows the co-authorship network connecting the top 25 collaborators of Nada Quercia. A scholar is included among the top collaborators of Nada Quercia 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 Nada Quercia. Nada Quercia is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Kernohan, Kristin D., Melanie Lacaria, Michelle M. Axford, et al.. (2025). Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years. Genetics in Medicine. 27(10). 101497–101497.

Hoed, Joery den, H Hashimoto, Mubeen Khan, et al.. (2024). Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes. Journal of Medical Genetics. 61(11). 1062–1067. 1 indexed citations

Papsin, Blake C., Sharon L. Cushing, Dimitri J. Stavropoulos, et al.. (2024). Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort. The Laryngoscope. 134(8). 3832–3838. 4 indexed citations

Hayeems, Robin Z., Stephanie Luca, Lauren Chad, et al.. (2023). Assessing the Performance of the Clinician-reported Genetic Testing Utility InDEx (C-GUIDE): Further Evidence of Inter-rater Reliability. Clinical Therapeutics. 45(8). 729–735. 2 indexed citations

Welters, Alena, Ranna El‐Khairi, Antonia Dastamani, et al.. (2019). Persistent hyperinsulinaemic hypoglycaemia in children with Rubinstein–Taybi syndrome. European Journal of Endocrinology. 181(2). 121–128. 13 indexed citations

Quercia, Nada, et al.. (2017). Primary ciliary dyskinesia: mechanisms and management. The Application of Clinical Genetics. Volume 10. 67–74. 46 indexed citations

Shugar, Andrea, et al.. (2016). Risk for Patient Harm in Canadian Genetic Counseling Practice: It's Time to Consider Regulation. Journal of Genetic Counseling. 26(1). 93–104. 9 indexed citations

Quercia, Nada, Gino R. Somers, William Halliday, et al.. (2010). Friedreich ataxia presenting as sudden cardiac death in childhood: Clinical, genetic and pathological correlation, with implications for genetic testing and counselling. Neuromuscular Disorders. 20(5). 340–342. 16 indexed citations

Yoon, Grace, Robyn Westmacott, Nada Quercia, et al.. (2009). Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit. BMJ Case Reports. 2009. bcr0820080688–bcr0820080688. 3 indexed citations

10.

Sermer, David, Nada Quercia, Karen Chong, & David Chitayat. (2007). Acrofacial dysostosis syndrome type Rodriguez: Prenatal diagnosis and autopsy findings. American Journal of Medical Genetics Part A. 143A(24). 3286–3289. 6 indexed citations

11.

Pavenski, Katerina, Lucie Dupuis, Shelley Kennedy, et al.. (2002). Detecting rearrangements in children using subtelomeric FISH and SKY. American Journal of Medical Genetics. 107(4). 267–274. 46 indexed citations

12.

McIntosh, Nathalie, et al.. (2002). DNA‐Sequence Patenting: National Society of Genetic Counselors (NSGC) Position Paper. Journal of Genetic Counseling. 11(4). 241–243. 1 indexed citations

13.

Pal, Tuya, Nancy Hamel, Danny Vesprini, et al.. (2001). Double primary cancers of the breast and thyroid in women: molecular analysis and genetic implications. Familial Cancer. 1(1). 17–24. 15 indexed citations

14.

Hill, Sharon R., Sheldon S. Leung, Nada Quercia, et al.. (2001). Ikirara Insertions Reveal Five New Anopheles gambiae Transposable Elements in Islands of Repetitious Sequence. Journal of Molecular Evolution. 52(3). 215–231. 11 indexed citations

15.

Quercia, Nada & Ahmad S. Teebi. (2001). Craniosynostosis, ectopia lentis, and congenital heart defects: Further delineation of an autosomal dominant syndrome with incomplete penetrance. American Journal of Medical Genetics. 107(1). 38–42. 2 indexed citations

16.

Quercia, Nada, David Chitayat, Riyana Babul‐Hirji, Maria I. New, & Denis Daneman. (1998). Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesis. Prenatal Diagnosis. 18(1). 83–85. 5 indexed citations

17.

Macmillan, Carol, T H Kirkham, Katherine Fu, et al.. (1998). Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy. Neurology. 50(2). 417–422. 76 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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