Jillian Nicholl

5.0k total citations · 2 hit papers
28 papers, 3.9k citations indexed

About

Jillian Nicholl is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Jillian Nicholl has authored 28 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Jillian Nicholl's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Jillian Nicholl is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Jillian Nicholl collaborates with scholars based in Australia, United States and Switzerland. Jillian Nicholl's co-authors include Ken Schooley, Craig A. Smith, Wenie S. Din, Raymond G. Goodwin, Pamela J. Smolak, Charles T. Rauch, Terri Smith, Steven R. Wiley, Grant R. Sutherland and David G. Campbell and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Immunity.

In The Last Decade

Jillian Nicholl

28 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Identification and characterization of a new member of the TNF family that induces apoptosis

1995 2.5k citations Steven R. Wiley, Ken Schooley et al. Immunity profile →
DNAM-1, A Novel Adhesion Molecule Involved in the Cytolytic Function of T Lymphocytes

1996 521 citations Akira Shibuya, David G. Campbell et al. Immunity profile →

Peers

Jillian Nicholl

IMMUN

ONCOL

GENET

Steven R. Wiley United States

Galen H. Fisher United States

Pamela J. Smolak United States

Laura L. McCormick United States

Christopher J. Donahue United States

Ben-Zion Levi Israel

Luika Timmerman United States

Timothy K. Starr United States

Barbara A. Malynn United States

Motoo Kitagawa Japan

Steven R. Wiley United States

Jillian Nicholl

3.3k ×1.3

2.2k ×1.3

IMMUN

1.3k ×1.8

828 ×1.2

ONCOL

450 ×0.9

GENET

Citations per year, relative to Jillian Nicholl Jillian Nicholl (= 1×) peers Steven R. Wiley

Countries citing papers authored by Jillian Nicholl

Since Specialization

Citations

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

Fields of papers citing papers by Jillian Nicholl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jillian Nicholl

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

Souzeau, Emmanuelle, Owen M. Siggs, Sean Mullany, et al.. (2022). Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort. Molecular Genetics & Genomic Medicine. 10(10). e2023–e2023. 4 indexed citations

Siggs, Owen M., Emmanuelle Souzeau, Deepa Taranath, et al.. (2020). Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma. Ophthalmology. 127(6). 758–766. 35 indexed citations

Mordaunt, Dylan, Shanti Balasubramaniam, David R. Thorburn, et al.. (2015). Phenotypic variation of TTC19‐deficient mitochondrial complex III deficiency: A case report and literature review. American Journal of Medical Genetics Part A. 167(6). 1330–1336. 26 indexed citations

Brueton, Louise, Jenny Morton, Dominic McMullan, et al.. (2015). Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders. European Journal of Human Genetics. 24(3). 373–380. 48 indexed citations

Haan, Eric, et al.. (2014). Phenotypes of AKT3 deletion: A case report and literature review. American Journal of Medical Genetics Part A. 167(1). 174–179. 36 indexed citations

Barnett, Christopher, et al.. (2012). Choreoathetosis, congenital hypothyroidism and neonatal respiratory distress syndrome with intact NKX2‐1. American Journal of Medical Genetics Part A. 158A(12). 3168–3173. 28 indexed citations

Nicholl, Jillian, Susan J. Brown, Michael Harbord, et al.. (2012). Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(1). 24–35. 17 indexed citations

McMahon, Jacinta M., Ingrid E. Scheffer, Jillian Nicholl, et al.. (2010). Detection of microchromosomal aberrations in refractory epilepsy: a pilot study. Epileptic Disorders. 12(3). 192–198. 14 indexed citations

Nandurkar, Harshal, Lorraine Robb, Jillian Nicholl, et al.. (1997). The gene for the human interleukin-11 receptor alpha chain locus is highly homologous to the murine gene and contains alternatively spliced first exons. The International Journal of Biochemistry & Cell Biology. 29(5). 753–766. 5 indexed citations

10.

Atkinson, M R, Andrea Townsend‐Nicholson, Jillian Nicholl, Grant R. Sutherland, & Peter R. Schofield. (1997). Cloning, characterisation and chromosomal assignment of the human adenosine A3 receptor (ADORA3) gene. Neuroscience Research. 29(1). 73–79. 36 indexed citations

11.

Quinn, Leonie M., Brett V. Johnson, Jillian Nicholl, Grant R. Sutherland, & Bill Kalionis. (1997). Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4. Gene. 187(1). 55–61. 62 indexed citations

12.

Stapleton, David, Erica Woollatt, Ken I. Mitchelhill, et al.. (1997). AMP‐activated protein kinase isoenzyme family: subunit structure and chromosomal location. FEBS Letters. 409(3). 452–456. 105 indexed citations

13.

Shibuya, Akira, David G. Campbell, Charles Hannum, et al.. (1996). DNAM-1, A Novel Adhesion Molecule Involved in the Cytolytic Function of T Lymphocytes. Immunity. 4(6). 573–581. 521 indexed citations breakdown →

14.

Gibson, Mark A., George Hatzinikolas, Jaliya Kumaratilake, et al.. (1996). Further Characterization of Proteins Associated with Elastic Fiber Microfibrils Including the Molecular Cloning of MAGP-2 (MP25). Journal of Biological Chemistry. 271(2). 1096–1103. 125 indexed citations

15.

Bernard, Ora, et al.. (1996). Structure and Chromosomal Localization of the Genomic Locus Encoding theKiz1LIM-Kinase Gene. Genomics. 35(3). 593–596. 11 indexed citations

16.

Mitchell, Christina A., Caroline J. Speed, Jillian Nicholl, & Grant R. Sutherland. (1996). Chromosomal Mapping of the Gene (INPP5A) Encoding the 43-kDa Membrane-Associated Inositol Polyphosphate 5-Phosphatase to 10q26.3 by Fluorescencein SituHybridization. Genomics. 31(1). 139–140. 7 indexed citations

17.

Wiley, Steven R., Ken Schooley, Pamela J. Smolak, et al.. (1995). Identification and characterization of a new member of the TNF family that induces apoptosis. Immunity. 3(6). 673–682. 2479 indexed citations breakdown →

18.

Dorow, Donna S., Lisa Devereux, Guo-Fen Tu, et al.. (1995). Complete Nucleotide Sequence, Expression, and Chromosomal Localisation of Human Mixed‐Lineage Kinase 2. European Journal of Biochemistry. 234(2). 492–500. 49 indexed citations

19.

Trapani, Joseph A., et al.. (1995). The closely linked genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expression. Immunogenetics. 41(1). 40–43. 25 indexed citations

20.

Webb, Graham C., Mark S. Baker, Jillian Nicholl, et al.. (1994). Chromosomal localization of the human urokinase plasminogen activator receptor and plasminogen activator inhibitor type‐2 genes: Implications in colorectal cancer. Journal of Gastroenterology and Hepatology. 9(4). 340–343. 8 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