Anna Hackett

4.1k total citations
20 papers, 514 citations indexed

About

Anna Hackett is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Anna Hackett has authored 20 papers receiving a total of 514 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Anna Hackett's work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (6 papers). Anna Hackett is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (6 papers). Anna Hackett collaborates with scholars based in Australia, United States and United Kingdom. Anna Hackett's co-authors include Jozef Gécz, Lindsay Rowe, F. Lucy Raymond, Michael Field, Mark Corbett, Vera M. Kalscheuer, Michael Field, Natalie Canham, John W. Nelson and Charles E. Schwartz and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Neurobiology of Aging.

In The Last Decade

Anna Hackett

20 papers receiving 488 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Hackett Australia 13 332 311 62 29 28 20 514
Huiqian Chen China 9 237 0.7× 172 0.6× 57 0.9× 22 0.8× 19 0.7× 11 444
Tatjana Bierhals Germany 13 271 0.8× 201 0.6× 41 0.7× 51 1.8× 42 1.5× 26 446
Frédéric Torès France 13 260 0.8× 209 0.7× 110 1.8× 35 1.2× 33 1.2× 22 478
Ganka Douglas United States 10 228 0.7× 161 0.5× 36 0.6× 23 0.8× 27 1.0× 13 336
Shino Shimada Japan 15 315 0.9× 318 1.0× 35 0.6× 68 2.3× 23 0.8× 36 545
Sébastien Chénier Canada 11 261 0.8× 278 0.9× 26 0.4× 56 1.9× 27 1.0× 17 473
Jéssica Molina United States 11 235 0.7× 177 0.6× 44 0.7× 17 0.6× 7 0.3× 20 414
Shashidhar Pai United States 8 278 0.8× 237 0.8× 61 1.0× 10 0.3× 25 0.9× 13 391
Arrate Pereda Spain 12 279 0.8× 242 0.8× 36 0.6× 68 2.3× 25 0.9× 31 430
Emma Bedoukian United States 13 238 0.7× 119 0.4× 26 0.4× 29 1.0× 30 1.1× 31 375

Countries citing papers authored by Anna Hackett

Since Specialization
Citations

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

Fields of papers citing papers by Anna Hackett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Hackett

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

All Works

20 of 20 papers shown
1.
Leffler, Melanie, Louise Christie, Anna Hackett, et al.. (2023). Further delineation of dosage‐sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance. Clinical Genetics. 103(6). 681–687. 1 indexed citations
2.
Niranjan, Tejasvi, Melanie May, Patrick Tarpey, et al.. (2019). Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Molecular Genetics & Genomic Medicine. 7(4). e00569–e00569. 10 indexed citations
3.
Hackett, Anna, et al.. (2019). Management of stroke in the Australian Indigenous population: from hospitals to communities. Internal Medicine Journal. 49(8). 962–968. 11 indexed citations
4.
Hackett, Anna, Marie Shaw, Alina Ilie, et al.. (2018). A recurrent missense variant inSLC9A7causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation. Human Molecular Genetics. 28(4). 598–614. 21 indexed citations
5.
Hashimoto, Satoru, Melanie May, Alexey Epanchintsev, et al.. (2017). MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression. Human Molecular Genetics. 26(11). 2062–2075. 17 indexed citations
6.
Dudding‐Byth, Tracy, Elizabeth Holliday, Anna Hackett, et al.. (2017). Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disability. BMC Biotechnology. 17(1). 90–90. 24 indexed citations
7.
Kumar, Raman, Thuong Ha, Duyen Pham, et al.. (2016). A non-coding variant in the 5ʹ UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability. European Journal of Human Genetics. 24(11). 1612–1616. 8 indexed citations
8.
Hocking, Darren R., Rachael Birch, Minh Bui, et al.. (2016). Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation. Neurobiology of Aging. 50. 5–12. 11 indexed citations
9.
Shaw, Marie, Lyndal Henden, Melanie Bahlo, et al.. (2015). Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome. European Journal of Medical Genetics. 58(6-7). 364–368. 13 indexed citations
10.
Birch, Rachael, Darren R. Hocking, Kim Cornish, et al.. (2015). Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males. Genes Brain & Behavior. 14(3). 251–259. 21 indexed citations
11.
Corbett, Mark, Tracy Dudding‐Byth, Patricia Crock, et al.. (2015). A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A. Journal of Medical Genetics. 52(4). 269–274. 40 indexed citations
12.
Grozeva, Detelina, Keren Carss, Olivera Spasić-Bošković, et al.. (2014). De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability. The American Journal of Human Genetics. 94(4). 618–624. 89 indexed citations
13.
Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations
14.
Shoubridge, Cheryl, Alison Gardner, Charles E. Schwartz, et al.. (2012). Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation?. European Journal of Human Genetics. 20(12). 1311–1314. 5 indexed citations
15.
Ellaway, Carolyn, Gladys Ho, Elisa Bettella, et al.. (2012). 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. European Journal of Human Genetics. 21(5). 522–527. 44 indexed citations
16.
Hackett, Anna, et al.. (2012). A transmission utility's experience to date with feeder unit protection systems. 31–31. 7 indexed citations
17.
Fullston, Tod, Merran Finnis, Anna Hackett, et al.. (2011). Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene. Clinical Genetics. 80(6). 510–522. 16 indexed citations
18.
Jensen, Lars Riff, H. Bartenschlager, Sinitdhorn Rujirabanjerd, et al.. (2010). A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. PubMed. 3(1). 2–2. 32 indexed citations
19.
Rujirabanjerd, Sinitdhorn, John W. Nelson, Patrick Tarpey, et al.. (2009). Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation. European Journal of Human Genetics. 18(3). 330–335. 50 indexed citations
20.
Hackett, Anna & Lindsay Rowe. (2006). FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report. Clinical Dysmorphology. 15(4). 207–210. 21 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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