Jane Juusola

5.6k total citations
41 papers, 1.7k citations indexed

About

Jane Juusola is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jane Juusola has authored 41 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 22 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jane Juusola's work include Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Molecular Biology Techniques and Applications (5 papers). Jane Juusola is often cited by papers focused on Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Molecular Biology Techniques and Applications (5 papers). Jane Juusola collaborates with scholars based in United States, Canada and Netherlands. Jane Juusola's co-authors include Jack Ballantyne, Kyle Retterer, Julie Scuffins, Bethany Friedman, Phanstiel, Megan T. Cho, Gabriele Richard, Kristin G. Monaghan, Wendy K. Chung and Kristin Lindstrom and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and Analytical Biochemistry.

In The Last Decade

Jane Juusola

38 papers receiving 1.7k citations

Peers

Jane Juusola

GENET

PPCH

ECOLO

Humaira Gowher United States

Eric Ostertag United States

Katherine E. Varley United States

Fumihito Miura Japan

Ray Kit Ng Hong Kong

B.S. Shastry United States

Tuan Huy Nguyen France

Tanja Waldmann Germany

Julio J. Mulero United States

Rebecca R. Selzer United States

Humaira Gowher United States

Jane Juusola

2.5k ×2.0

602 ×0.7

GENET

198 ×1.2

134 ×0.9

PPCH

57 ×0.4

ECOLO

Citations per year, relative to Jane Juusola Jane Juusola (= 1×) peers Humaira Gowher

Countries citing papers authored by Jane Juusola

Since Specialization

Citations

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

Fields of papers citing papers by Jane Juusola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jane Juusola

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Tenorio, Jair, Rita María Regojo, Jane Juusola, et al.. (2024). Non‐immune hydrops fetalis is associated with bi‐allelic pathogenic variants in the MYB Binding Protein 1a ( MYBBP1A ) gene. Clinical Genetics. 106(6). 713–720.

McWalter, Kirsty, Erin Torti, Michelle M. Morrow, Jane Juusola, & Kyle Retterer. (2022). Discovery of over 200 new and expanded genetic conditions using GeneMatcher. Human Mutation. 43(6). 760–764. 6 indexed citations

Lebaron, Simon, Marie-Françoise O’Donohue, Kendra Engleman, et al.. (2021). Functionally impaired RPL8 variants associated with Diamond–Blackfan anemia and a Diamond–Blackfan anemia‐like phenotype. Human Mutation. 43(3). 389–402. 5 indexed citations

Bupp, Caleb, et al.. (2021). First case of pan-suture craniosynostosis due to de novo mosaic KAT6A mutation. Child s Nervous System. 38(1). 173–177. 3 indexed citations

O'Neil, Erin, et al.. (2021). Compound Heterozygous Mutations in ZNF408 in a Patient with a Late Onset Pigmentary Retinopathy and Relatively Preserved Central Retina. Documenta Ophthalmologica. 143(3). 305–312. 3 indexed citations

Hurwitz, Stephanie N., et al.. (2020). Aplastic anemia in a patient with CVID due to NFKB1 haploinsufficiency. Molecular Case Studies. 6(6). a005769–a005769. 7 indexed citations

Torene, Rebecca I., Kevin Galens, Shuxi Liu, et al.. (2020). Mobile element insertion detection in 89,874 clinical exomes. Genetics in Medicine. 22(5). 974–978. 39 indexed citations

Ritter, Alyssa, Emma Bedoukian, Justin H. Berger, et al.. (2019). Clinical utility of exome sequencing in infantile heart failure. Genetics in Medicine. 22(2). 423–426. 13 indexed citations

Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2019). Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. American Journal of Medical Genetics Part A. 179(6). 927–935. 32 indexed citations

10.

Baker, Elizabeth, et al.. (2019). An unusual case of nephrotic syndrome in a microcephalic infant: Questions. Pediatric Nephrology. 34(11). 2325–2326.

11.

Murdock, David R., Yunyun Jiang, Michael F. Wangler, et al.. (2019). Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition. Molecular Case Studies. 5(3). a003608–a003608. 13 indexed citations

12.

Bayrak‐Toydemir, Pınar, Lora Jh Bean, Alicia Braxton, et al.. (2018). Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization. Genetics in Medicine. 21(4). 861–866. 14 indexed citations

13.

Eyaid, Wafaa, Kimberli J. Kamer, Rehab Ali, et al.. (2018). A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. JIMD Reports. 43. 79–83. 43 indexed citations

14.

Okur, Volkan, Megan T. Cho, Lindsay B. Henderson, et al.. (2016). De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. Human Genetics. 135(7). 699–705. 53 indexed citations

15.

Millan, Francisca, Megan T. Cho, Kyle Retterer, et al.. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American Journal of Medical Genetics Part A. 170(7). 1791–1798. 42 indexed citations

16.

Juusola, Jane, et al.. (2008). Recovery and Stability of RNA in Vaginal Swabs and Blood, Semen, and Saliva Stains. Journal of Forensic Sciences. 53(2). 296–305. 125 indexed citations

17.

Juusola, Jane & Jack Ballantyne. (2007). mRNA Profiling for Body Fluid Identification by Multiplex Quantitative RT‐PCR*. Journal of Forensic Sciences. 52(6). 1252–1262. 175 indexed citations

18.

Juusola, Jane & Jack Ballantyne. (2005). Multiplex mRNA profiling for the identification of body fluids. Forensic Science International. 152(1). 1–12. 272 indexed citations

19.

Juusola, Jane, et al.. (2004). An mRNA and DNA co-isolation method for forensic casework samples. Analytical Biochemistry. 335(2). 289–298. 76 indexed citations

20.

Juusola, Jane & Jack Ballantyne. (2003). Messenger RNA profiling: a prototype method to supplant conventional methods for body fluid identification. Forensic Science International. 135(2). 85–96. 216 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.

Explore authors with similar magnitude of impact