Jillian Nicholl

5.0k citations

28 papers · 3.9k indexed · 2 hit papers · h-index 18

Immunology top 1%
- interferon and immune responses 3
Cancer Research top 2%
- Protease and Inhibitor Mechanisms 4
Molecular Biology top 5%
Oncology top 5%
- Peptidase Inhibition and Analysis 3
Immunology and Allergy top 5%
- Cell Adhesion Molecules Research 3
Genetics
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 4
- Connective tissue disorders research 3

Co-authors: Ken Schooley Craig A. Smith Wenie S. Din Raymond G. Goodwin Pamela J. Smolak Charles T. Rauch Terri Smith Steven R. Wiley
Cited by: Immunology Cancer Research Molecular Biology
Partner nations: Australia United States Switzerland

In The Last Decade

Jillian Nicholl

28 papers receiving 3.8k citations

Hit Papers

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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.

1996 DNAM-1, A Novel Adhesion Molecule Involved in the Cytolytic Function of T Lymphocytes
1995 Identification and characterization of a new member of the TNF family that induces apoptosis

Peers

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

The 25 scholars most cited alongside Jillian Nicholl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jillian Nicholl Line = papers co-authored together Jillian Nicholl links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort Emmanuelle Souzeau,Owen M. Siggs,Sean Mullany,Joshua M. Schmidt,Mark Hassall,Andrew Dubowsky,Angela Chappell,James Breen,Haae Bae,Jillian Nicholl,Johanna Hadler,Lisa S. Kearns,Sandra E. Staffieri,Alex W. Hewitt,David A. Mackey,Aanchal Gupta,Kathryn P. Burdon,Sonja Klebe,Jamie E. Craig,Richard Mills	2022	4
2	Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma Owen M. Siggs,Emmanuelle Souzeau,Deepa Taranath,Andrew Dubowsky,Angela Chappell,Tiger Zhou,Shari Javadiyan,Jillian Nicholl,Lisa S. Kearns,Sandra E. Staffieri,Andrew Narita,James E. Smith,John Pater,Alex W. Hewitt,Jonathan B. Ruddle,James E. Elder,David A. Mackey,Kathryn P. Burdon,Jamie E. Craig	2020	35
3	Phenotypic variation of TTC19‐deficient mitochondrial complex III deficiency: A case report and literature review Dylan Mordaunt,Alexandra Jolley,Shanti Balasubramaniam,David R. Thorburn,Hayley S. Mountford,Alison G. Compton,Jillian Nicholl,Nicholas Manton,Damian Clark,Drago Bratkovic,Kathryn Friend,Sui Yu	2015	26
4	Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders Ching Moey,Susan J. Hinze,Louise Brueton,Jenny Morton,Dominic McMullan,Benjamin Kamien,Christopher Barnett,Nicola Brunetti‐Pierri,Jillian Nicholl,Jozef Gécz,Cheryl Shoubridge	2015	48
5	Phenotypes of AKT3 deletion: A case report and literature review Dayu Gai,Eric Haan,M Scholar,Jillian Nicholl,Sui Yu	2014	36
6	Choreoathetosis, congenital hypothyroidism and neonatal respiratory distress syndrome with intact NKX2‐1 Christopher Barnett,Justin J. Mencel,Jozef Gécz,Wendy Waters,Susan M. Kirwin,Kathy M. B. Vinette,Miriam Uppill,Jillian Nicholl	2012	28
7	Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH Jillian Nicholl,Wendy Waters,Shanna Suwalski,Susan J. Brown,Yvonne Hull,Michael Harbord,John Entwistle,Suzanna Thompson,Damian Clark,Claire Pridmore,Eric Haan,Christopher Barnett,Lesley McGregor,Jan Liebelt,Elizabeth M. Thompson,Kathryn Friend,Sharon Bain,Sui Yu,John C. Mulley	2012	17
8	Detection of microchromosomal aberrations in refractory epilepsy: a pilot study Jacinta M. McMahon,Ingrid E. Scheffer,Jillian Nicholl,Wendy Waters,Helen J. Eyre,Lyn Hinton,Paul V. Nelson,Sui Yu,Leanne M. Dibbens,Samuel F. Berkovic,John C. Mulley	2010	14
9	The gene for the human interleukin-11 receptor alpha chain locus is highly homologous to the murine gene and contains alternatively spliced first exons Harshal Nandurkar,Lorraine Robb,Jillian Nicholl,Douglas J. Hilton,Grant R. Sutherland,C. Glenn Begley	1997	5
10	Cloning, characterisation and chromosomal assignment of the human adenosine A3 receptor (ADORA3) gene M R Atkinson,Andrea Townsend‐Nicholson,Jillian Nicholl,Grant R. Sutherland,Peter R. Schofield	1997	36
11	Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4 Leonie M. Quinn,Brett V. Johnson,Jillian Nicholl,Grant R. Sutherland,Bill Kalionis	1997	62
12	AMP‐activated protein kinase isoenzyme family: subunit structure and chromosomal location David Stapleton,Erica Woollatt,Ken I. Mitchelhill,Jillian Nicholl,Carolina Fernández,Belinda J. Michell,Lee A. Witters,David A. Power,Grant R. Sutherland,Bruce E. Kemp	1997	105
13	DNAM-1, A Novel Adhesion Molecule Involved in the Cytolytic Function of T Lymphocytesbreakdown → Akira Shibuya,David G. Campbell,Charles Hannum,Hans Yssel,Karin Franz-Bacon,Terrill K. McClanahan,Toshio Kitamura,Jillian Nicholl,Grant R. Sutherland,Lewis L. Lanier,Joseph H. Phillips	1996	521
14	Further Characterization of Proteins Associated with Elastic Fiber Microfibrils Including the Molecular Cloning of MAGP-2 (MP25) Mark A. Gibson,George Hatzinikolas,Jaliya Kumaratilake,Lawrence B. Sandberg,Jillian Nicholl,Grant R. Sutherland,Edward G. Cleary	1996	125
15	Structure and Chromosomal Localization of the Genomic Locus Encoding theKiz1LIM-Kinase Gene Ora Bernard,Vicki Burkitt,Graham C. Webb,C. D. K. Bottema,Jillian Nicholl,Grant R. Sutherland,P Matthew	1996	11
16	Chromosomal Mapping of the Gene (INPP5A) Encoding the 43-kDa Membrane-Associated Inositol Polyphosphate 5-Phosphatase to 10q26.3 by Fluorescencein SituHybridization Christina A. Mitchell,Caroline J. Speed,Jillian Nicholl,Grant R. Sutherland	1996	7
17	Identification and characterization of a new member of the TNF family that induces apoptosisbreakdown → Steven R. Wiley,Ken Schooley,Pamela J. Smolak,Wenie S. Din,Chang-Pin Huang,Jillian Nicholl,Grant R. Sutherland,Terri Smith,Charles T. Rauch,Craig A. Smith,Raymond G. Goodwin	1995	2479
18	Complete Nucleotide Sequence, Expression, and Chromosomal Localisation of Human Mixed‐Lineage Kinase 2 Donna S. Dorow,Lisa Devereux,Guo-Fen Tu,Gareth Price,Jillian Nicholl,Grant R. Sutherland,Richard J. Simpson	1995	49
19	The closely linked genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expression Michelle J. Dawson,Joseph A. Trapani,Robert C. Briggs,Jillian Nicholl,Grant R. Sutherland,Elizabeth Baker	1995	25
20	Chromosomal localization of the human urokinase plasminogen activator receptor and plasminogen activator inhibitor type‐2 genes: Implications in colorectal cancer Graham C. Webb,Mark S. Baker,Jillian Nicholl,Yao Wang,Graeme Woodrow,EGBERT KRUITHOF,William F. Doe	1994	8

About Jillian Nicholl

Jillian Nicholl is a scholar working on Immunology and Allergy, Physiology and Cancer Research, having authored 28 papers that have together received 3.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Protease and Inhibitor Mechanisms (4 papers), interferon and immune responses (3 papers), Connective tissue disorders research (3 papers), Peptidase Inhibition and Analysis (3 papers) and Cell Adhesion Molecules Research (3 papers). The work is most often cited by research in Immunology (1.6k citations), Cancer Research (716 citations) and Molecular Biology (2.5k citations). Jillian Nicholl has collaborated with scholars based in Australia, United States and Switzerland. Frequent 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.

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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