Anna Hackett

4.2k citations

43 papers · 3.2k · 1 hit paper · h-index 26

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Molecular Biology top 5%
- RNA modifications and cancer
- RNA Research and Splicing
- Congenital heart defects research
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation

Papers in

Genetics 34
- Genetics and Neurodevelopmental Disorders 28
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 12
Molecular Biology 21
- RNA modifications and cancer 5
- Congenital heart defects research 5
- Ubiquitin and proteasome pathways 4

Co-authors: Jozef Gécz (12 shared papers)Michael J. Field (6 shared papers)Frances Lucy Raymond (3 shared papers)Lindsay S. Rowe (1 shared paper)Mark A Corbett (4 shared papers)John W. Nelson (3 shared papers)Kathryn L. Friend (4 shared papers)Michael H. Field (2 shared papers)
Journals: European Journal of Human Genetics (8 papers)The American Journal of Human Genetics (6 papers)Human Molecular Genetics (4 papers)Nature Genetics (3 papers)Molecular Psychiatry (3 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

Anna Hackett

42 papers receiving 3.1k citations

Anna Hackett's Hit Papers

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A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation 2009 · 508 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2009 Nature Genetics

Peers

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-authors

The 25 scholars most cited alongside Anna Hackett, 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 Anna Hackett Line = papers co-authored together Anna Hackett links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation Nature Genetics ·Patrick S. Tarpey, Raffaella Smith, Erin Pleasance, Annabel C. Whibley, Sarah Edkins, Claire W. Hardy, Sarah O’Meara, Calli Latimer Hit paper breakdown →	2009	508
2	X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes Molecular Psychiatry ·Hao Yu Hu, Stefan A. Haas, Jamel Chelly, Hilde Van Esch, Martine Raynaud, Arjan P.M. de Brouwer, Stefanie Weinert, Guy Froyen	2015	244
3	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation Nature Genetics ·Patrick S. Tarpey, Frances Lucy Raymond, Lam Son Nguyen, Jayson D. Rodriguez, Anna Hackett, Lucianne Vandeleur, Raffaella Smith, Cheryl Shoubridge	2007	230
4	Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS The American Journal of Human Genetics ·Haloom Rafehi, David J. Szmulewicz, Mark F. Bennett, Nara L. M. Sobreira, Kate Pope, Katherine Rose Smith, Greta Gillies, Peter Diakumis	2019	189
5	Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation The American Journal of Human Genetics ·Guy Froyen, Mark A Corbett, Joke Vandewalle, Irma E. Järvelä, Owen Lawrence, Cliff J. Meldrum, Marijke Bauters, Karen Govaerts	2008	179
6	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome Journal of Medical Genetics ·David Aljosja Koolen, Andrew J. Sharp, Jane A. Hurst, Helen Firth, Samantha J.L. Knight, Alice Goldenberg, Pascale Saugier-Véber, Rolph Pfundt	2008	178
7	Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability Human Mutation ·Detelina Grozeva, Keren Carss, Olivera Spasić-Bošković, María‐Isabel Tejada, Jozef Gécz, Marie A Shaw, Mark A Corbett, Eric Haan	2015	147
8	Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability Nature Genetics ·Cheryl Shoubridge, Patrick S. Tarpey, Fatima Abidi, Sarah L. Ramsden, Sinitdhorn Rujirabanjerd, Jessica A. Murphy, Jackie Boyle, Marie A Shaw	2010	128
9	Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor Human Molecular Genetics ·Asif Ali, P. T. Christie, I. V. Grigorieva, Brian N Harding, Hilde Van Esch, S. F. Ahmed, Maria A. K. Bitner-Glindzicz, EBERHARD BLIND	2006	116
10	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 ·Detelina Grozeva, Keren Carss, Olivera Spasić-Bošković, Michael J. Parker, Hayley L Archer, Helen Firth, Soo‐Mi Park, Natalie L.E. Canham	2014	106
11	Fine-Scale Survey of X Chromosome Copy Number Variants and Indels Underlying Intellectual Disability The American Journal of Human Genetics ·Annabel C. Whibley, Vincent Plagnol, Patrick S. Tarpey, Fatima Abidi, Tod Fullston, Maja K. Choma, Catherine A. Boucher, Lorraine Shepherd	2010	105
12	Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability Molecular Psychiatry ·Lam Son Nguyen, Lachlan A. Jolly, Cheryl Shoubridge, Wai-Kin Chan, Lulu Huang, Frédéric Laumonnier, Martine Raynaud, Anna Hackett	2011	103
13	CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes European Journal of Human Genetics ·Anna Hackett, Patrick S. Tarpey, Andrea Licata, James J. Cox, Annabel C. Whibley, Jackie Boyle, Carolyn Rogers, John Grigg	2009	95
14	A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability The American Journal of Human Genetics ·Lingli Huang, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, Alison E. Gardner, Raman Kumar, Evelyn Douglas, Cheryl Shoubridge, Dagmar Wieczorek	2012	87
15	Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis European Journal of Human Genetics ·Lisa Ewans, André E. Minoche, DEBORAH J. SCHOFIELD, Rupendra N. Shrestha, Clare Puttick, Ying Zhu, Alexander P. Drew, Velimir Gayevskiy	2022	86
16	Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation European Journal of Human Genetics ·Sinitdhorn Rujirabanjerd, John W. Nelson, Patrick S. Tarpey, Anna Hackett, Sarah Edkins, Frances Lucy Raymond, Charles E. Schwartz, GILLIAN M. TURNER	2009	60
17	THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability The American Journal of Human Genetics ·Raman Kumar, Mark A Corbett, Bregje W.M. van Bon, Joshua A. Woenig, Lloyd Weir, Evelyn Douglas, Kathryn L. Friend, Alison E. Gardner	2015	58
18	CCDC22: a novel candidate gene for syndromic X-linked intellectual disability Molecular Psychiatry ·Irina Voineagu, Lingli Huang, Kellen Diamond Winden, María T. Lázaro, Eric Haan, John W. Nelson, Julie M. McGaughran, Lam Son Nguyen	2011	50
19	14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype European Journal of Human Genetics ·Carolyn Ellaway, Gladys Ho, Elisa Bettella, Alisa Knapman, Felicity A. Collins, Anna Hackett, F. Ellis McKenzie, Artur Darmanian	2012	48
20	A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A Journal of Medical Genetics ·Mark A Corbett, Tracy Dudding‐Byth, Patricia Crock, Elena Botta, Louise Christie, Tiziana Nardò, Giuseppina Caligiuri, Lynne Hobson	2015	48

About Anna Hackett

Anna Hackett is a scholar working on Genetics, Molecular Biology, Cell Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 43 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (28 papers), Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (12 papers), RNA modifications and cancer (5 papers), Congenital heart defects research (5 papers), Ubiquitin and proteasome pathways (4 papers), Chromosomal and Genetic Variations (3 papers) and Cellular transport and secretion (3 papers). The work is most often cited by research in Genetics (1.7k citations), Molecular Biology (1.9k citations), Cellular and Molecular Neuroscience (307 citations), Cell Biology (257 citations) and Cognitive Neuroscience (202 citations). Anna Hackett has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Jozef Gécz, Michael J. Field, Frances Lucy Raymond, Lindsay S. Rowe, Mark A Corbett, John W. Nelson, Kathryn L. Friend, Michael H. Field, GILLIAN M. TURNER and Lingli Huang. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Molecular Genetics, Nature Genetics and Molecular Psychiatry.

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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Anna Hackett's Hit Papers

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About Anna Hackett

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