Janine Smith

3.4k total citations
20 papers, 253 citations indexed

About

Janine Smith is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Janine Smith has authored 20 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Surgery and 4 papers in Genetics. Recurrent topics in Janine Smith's work include Congenital Heart Disease Studies (3 papers), Congenital heart defects research (3 papers) and Genomics and Rare Diseases (2 papers). Janine Smith is often cited by papers focused on Congenital Heart Disease Studies (3 papers), Congenital heart defects research (3 papers) and Genomics and Rare Diseases (2 papers). Janine Smith collaborates with scholars based in Australia, United States and United Kingdom. Janine Smith's co-authors include Thomas L. Steinemann, Shireen R. Lamandé, Rachel A. Peat, Kathryn N. North, Naomi L. Baker, S. J. Kaufman, Alison G. Compton, Dean J. Burkin, Rishika A. Pace and B. J. Cooper and has published in prestigious journals such as Neurology, PEDIATRICS and International Journal of Molecular Sciences.

In The Last Decade

Janine Smith

16 papers receiving 241 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Janine Smith Australia	8	110	52	42	34	30	20	253
M Buchfelder Germany	12	56 0.5×	112 2.2×	14 0.3×	33 1.0×	35 1.2×	43	381
Marion Gérard‐Blanluet France	13	200 1.8×	61 1.2×	158 3.8×	12 0.4×	31 1.0×	24	399
A Tullio-Pelet France	6	174 1.6×	146 2.8×	60 1.4×	21 0.6×	50 1.7×	9	369
Rieko Kominami Japan	12	131 1.2×	53 1.0×	35 0.8×	16 0.5×	6 0.2×	24	404
Fawzi Bakiri Algeria	5	152 1.4×	94 1.8×	49 1.2×	8 0.2×	26 0.9×	6	305
Mariateresa Falco Italy	9	94 0.9×	46 0.9×	175 4.2×	25 0.7×	20 0.7×	22	334
C. M. Hall United Kingdom	12	177 1.6×	71 1.4×	121 2.9×	14 0.4×	13 0.4×	14	490
Athina Xaidara Greece	10	121 1.1×	55 1.1×	55 1.3×	41 1.2×	19 0.6×	21	355
Masashi Kitagawa Japan	8	104 0.9×	47 0.9×	39 0.9×	17 0.5×	16 0.5×	21	234
Ryogo Shobatake Japan	12	54 0.5×	62 1.2×	50 1.2×	13 0.4×	5 0.2×	24	333

Countries citing papers authored by Janine Smith

Since Specialization

Citations

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

Fields of papers citing papers by Janine Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janine Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Janine Smith. A scholar is included among the top collaborators of Janine Smith 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 Janine Smith. Janine Smith 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

Bennetts, Bruce, et al.. (2025). Outcomes and experiences of genetic testing in children with congenital heart disease. Journal of Medical Genetics. 62(5). 335–344.

Riley, Lisa G., Subrata Sabui, Hamid M. Said, et al.. (2024). Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy. European Journal of Human Genetics. 32(8). 947–953.

Ma, Alan, Rosie O’Shea, Bruce Bennetts, et al.. (2024). Genomic multidisciplinary teams: A model for navigating genetic mainstreaming and precision medicine. Journal of Paediatrics and Child Health. 60(4-5). 118–124. 7 indexed citations

Heslehurst, Nicola, Theophile Bigirumurame, M. Dawn Teare, et al.. (2023). Study of How Adiposity in Pregnancy has an Effect on outcomeS (SHAPES): protocol for a prospective cohort study. BMJ Open. 13(9). e073545–e073545. 1 indexed citations

Vasudevan, Anand, Kristen Neville, Brigitte Gerstl, et al.. (2023). Genotype–phenotype correlations in paediatric and adolescent phaeochromocytoma and paraganglioma: a cross-sectional study. Archives of Disease in Childhood. 109(3). 201–208. 2 indexed citations

Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations

Smith, Janine, Annabelle Enriquez, Gary F. Sholler, et al.. (2021). A new era of genetic testing in congenital heart disease: A review. Trends in Cardiovascular Medicine. 32(5). 311–319. 7 indexed citations

Blue, Gillian M., Janine Smith, Gary F. Sholler, Christopher Semsarian, & David S. Winlaw. (2020). Current Practice of Genetic Testing and Counselling in Congenital Heart Disease: An Australian Perspective. Heart Lung and Circulation. 29(11). 1733–1736.

Smith, Janine, et al.. (2018). Speech and Language Screenings in Head Start Programs: A Descriptive Study. Journal of Education and Human Development. 7(2).

10.

Meyer‐Rochow, Goswin Y., Janine Smith, Deborah J. Marsh, et al.. (2008). Denaturing High Performance Liquid Chromatography Detection of SDHB, SDHD, and VHL Germline Mutations in Pheochromocytoma. Journal of Surgical Research. 157(1). 55–62. 13 indexed citations

11.

Meyer‐Rochow, Goswin Y., Janine Smith, Deborah J. Marsh, et al.. (2008). QS297. Denaturing High Performance Liquid Chromatography for the Detection of Germline Mutations in Phaeochromocytoma. Journal of Surgical Research. 144(2). 385–385. 1 indexed citations

12.

Peat, Rachel A., Janine Smith, Alison G. Compton, et al.. (2007). Diagnosis and etiology of congenital muscular dystrophy. Neurology. 71(5). 312–321. 61 indexed citations

13.

Godfrey, C., R. Mein, Martin Brockington, et al.. (2006). P.O.1 Molecular genetic analysis of 6 glycosyltransferases in a large population of dystroglycanopathy patients significantly widens the spectrum of phenotypes resulting from POMT1, POMGnT1 and Fukutin mutations. Neuromuscular Disorders. 16(9-10). 683–683. 1 indexed citations

14.

Neas, Katherine, Janine Smith, Nicole Chia, et al.. (2005). Three patients with terminal deletions within the subtelomeric region of chromosome 9q. American Journal of Medical Genetics Part A. 132A(4). 425–430. 24 indexed citations

15.

Smith, Janine, Delphine Trochet, Robert Ouvrier, et al.. (2005). Congenital Central Hypoventilation Syndrome and Hirschsprung’s Disease in an Extremely Preterm Infant. PEDIATRICS. 115(6). e737–e738. 25 indexed citations

16.

Smith, Janine & Thomas L. Steinemann. (2000). Vitamin A Deficiency and the Eye. International Ophthalmology Clinics. 40(4). 83–91. 67 indexed citations

17.

Smith, Janine. (1982). The Epidemiology of Allergic Rhinitis. Allergy and Asthma Proceedings. 3(3). 383–388. 10 indexed citations

18.

Johnson, Rudolph P., A. D. J. Watson, Janine Smith, & B. J. Cooper. (1975). Myasthenia in Springer Spaniel littermates. Journal of Small Animal Practice. 16(1-12). 641–647. 23 indexed citations

19.

Smith, Janine & J. Robert Smyth. (1970). Knobby, A Semilethal Mutation Resulting in Defective Down in the Turkey. Journal of Heredity. 61(3). 119–122. 3 indexed citations

20.

Smith, Janine, et al.. (1956). C-reactive protein in allergic diseases. Journal of Allergy. 27(4). 338–343. 1 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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