Lynette S. Penney

2.0k total citations
13 papers, 273 citations indexed

About

Lynette S. Penney is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lynette S. Penney has authored 13 papers receiving a total of 273 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lynette S. Penney's work include Amino Acid Enzymes and Metabolism (2 papers), BRCA gene mutations in cancer (2 papers) and Metabolism and Genetic Disorders (2 papers). Lynette S. Penney is often cited by papers focused on Amino Acid Enzymes and Metabolism (2 papers), BRCA gene mutations in cancer (2 papers) and Metabolism and Genetic Disorders (2 papers). Lynette S. Penney collaborates with scholars based in Canada, United States and United Kingdom. Lynette S. Penney's co-authors include Patrick S. Parfrey, Michael O. Woods, Terry‐Lynn Young, Donna Hefferton, Jane S. Green, William S. Davidson, Jacqueline Talarchek, Mitchell Cheung, Joseph R. Testa and Mark D. Ludman and has published in prestigious journals such as The American Journal of Human Genetics, Obstetrics and Gynecology and Human Genetics.

In The Last Decade

Lynette S. Penney

13 papers receiving 259 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lynette S. Penney Canada	7	143	112	45	31	22	13	273
Zhangzhang Lan China	8	202 1.4×	103 0.9×	15 0.3×	16 0.5×	33 1.5×	16	304
Monique De Vroede Netherlands	10	158 1.1×	84 0.8×	28 0.6×	40 1.3×	19 0.9×	17	361
Shinsuke Ninomiya Japan	14	268 1.9×	210 1.9×	43 1.0×	16 0.5×	48 2.2×	31	444
Ok‐Hwa Kim South Korea	10	194 1.4×	124 1.1×	24 0.5×	37 1.2×	17 0.8×	12	318
Laura Lecce Australia	11	154 1.1×	33 0.3×	25 0.6×	24 0.8×	33 1.5×	20	312
Robin Steinhaus Germany	7	142 1.0×	97 0.9×	20 0.4×	9 0.3×	33 1.5×	11	249
Majdi Nagara Tunisia	10	161 1.1×	140 1.3×	36 0.8×	63 2.0×	26 1.2×	25	343
Adi Har‐Zahav Israel	8	139 1.0×	65 0.6×	19 0.4×	20 0.6×	26 1.2×	14	256
Francesca Clementina Radio Italy	15	194 1.4×	149 1.3×	15 0.3×	14 0.5×	24 1.1×	40	421

Countries citing papers authored by Lynette S. Penney

Since Specialization

Citations

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

Fields of papers citing papers by Lynette S. Penney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lynette S. Penney. 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 Lynette S. Penney. The network helps show where Lynette S. Penney may publish in the future.

Co-authorship network of co-authors of Lynette S. Penney

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

All Works

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13 of 13 papers shown

Penney, Lynette S., et al.. (2022). Hereditary ovarian cancer risk reduction: a retrospective evaluation of patient perspectives and service provision at a regional hereditary gynaecologic cancer clinic 2006–2016. BMC Women s Health. 22(1). 263–263. 1 indexed citations

Ferguson, Meghan, et al.. (2021). Universal access to genetic counseling for women with epithelial ovarian cancer in Nova Scotia: Evaluating a new collaborative care model. Journal of Genetic Counseling. 30(5). 1491–1499. 2 indexed citations

Johnson, Liane B., et al.. (2019). Severe cryopyrin-associated periodic syndrome first characterized by early childhood-onset sensorineural hearing loss – Case report and literature review. International Journal of Pediatric Otorhinolaryngology. 120. 68–72. 5 indexed citations

Smith, Amanda, Yoko Itō, Jeremy Schwartzentruber, et al.. (2018). A family segregating lethal neonatal coenzyme Q₁₀ deficiency caused by mutations in COQ9. Journal of Inherited Metabolic Disease. 41(4). 719–729. 33 indexed citations

Imran, Syed Ali, Lynette S. Penney, Sidney Croul, et al.. (2018). Unusual AIP mutation and phenocopy in the family of a young patient with acromegalic gigantism. Endocrinology Diabetes and Metabolism Case Reports. 2018. 3 indexed citations

Penney, Lynette S., et al.. (2016). Severe laryngeal stenosis in newly born twins with 22q11.2 deletion syndrome: A case report. Journal of Neonatal-Perinatal Medicine. 9(2). 223–226. 2 indexed citations

Penney, Lynette S., et al.. (2014). Vitamin B12 deficiency with intrinsic factor antibodies in an infant with poor growth and developmental delay. Paediatrics & Child Health. 19(2). 84–86. 8 indexed citations

Tokita, Mari, Ghayda Mirzaa, Nicola Dikow, et al.. (2014). Five children with deletions of 1p34.3 encompassing AGO1 and AGO3. European Journal of Human Genetics. 23(6). 761–765. 28 indexed citations

LeBlanc, Marissa A., Lynette S. Penney, Daniel Gaston, et al.. (2013). A novel rearrangement of occludin causes brain calcification and renal dysfunction. Human Genetics. 132(11). 1223–1234. 22 indexed citations

10.

Cheung, Mitchell, et al.. (2013). Further evidence for germline BAP1 mutations predisposing to melanoma and malignant mesothelioma. Cancer Genetics. 206(5). 206–210. 59 indexed citations

11.

Warren, Andrew E., et al.. (2010). Left Ventricular Noncompaction and Coronary Artery Fistula in an Infant with Deletion 22q11.2. Pediatric Cardiology. 32(2). 208–210. 14 indexed citations

12.

Allen, Victoria M., Lynette S. Penney, Ivan L. Rapchuk, et al.. (2009). Successful Outcome in Pregnancy With Arterial Tortuosity Syndrome. Obstetrics and Gynecology. 114(2). 494–498. 6 indexed citations

13.

Young, Terry‐Lynn, Lynette S. Penney, Michael O. Woods, et al.. (1999). A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31. The American Journal of Human Genetics. 64(3). 900–904. 90 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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