Louise Christie

1.0k total citations
14 papers, 409 citations indexed

About

Louise Christie is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Louise Christie has authored 14 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Louise Christie's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (3 papers). Louise Christie is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (3 papers). Louise Christie collaborates with scholars based in Australia, United Kingdom and United States. Louise Christie's co-authors include Gillian Turner, Michael Field, Anne‐Marie Bisgaard, Alyssa C. Hill, Georg Wieczorek, Ines Müller, Hans‐Hilger Ropers, Ana Cristina Victorino Krepischi, Avril V. Brereton and Angela Maria Vianna‐Morgante and has published in prestigious journals such as Human Molecular Genetics, International Journal of Environmental Research and Public Health and Journal of Medical Genetics.

In The Last Decade

Louise Christie

14 papers receiving 401 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Louise Christie Australia	10	294	197	73	68	40	14	409
Olaya Villa Spain	9	237 0.8×	150 0.8×	126 1.7×	49 0.7×	36 0.9×	17	336
Alisha Wilkens United States	13	255 0.9×	239 1.2×	104 1.4×	26 0.4×	67 1.7×	20	438
Tiziana Filippi Italy	9	374 1.3×	207 1.1×	157 2.2×	67 1.0×	71 1.8×	10	539
Laëtitia Lambert France	11	351 1.2×	235 1.2×	38 0.5×	77 1.1×	26 0.7×	32	509
I. López Spain	10	207 0.7×	202 1.0×	57 0.8×	39 0.6×	23 0.6×	23	336
Eleni Katzaki Italy	11	231 0.8×	148 0.8×	31 0.4×	57 0.8×	36 0.9×	11	316
Shashidhar Pai United States	8	237 0.8×	278 1.4×	49 0.7×	61 0.9×	35 0.9×	13	391
Ellen Taub Israel	8	263 0.9×	207 1.1×	88 1.2×	121 1.8×	10 0.3×	12	446
D F Smeets Netherlands	10	391 1.3×	296 1.5×	92 1.3×	47 0.7×	48 1.2×	11	478
Amber Boys Australia	7	154 0.5×	143 0.7×	35 0.5×	41 0.6×	17 0.4×	10	281

Countries citing papers authored by Louise Christie

Since Specialization

Citations

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

Fields of papers citing papers by Louise Christie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Christie

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

All Works

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14 of 14 papers shown

Schofield, Deborah, Rupendra Shrestha, Owen Tan, et al.. (2024). The Healthcare and Societal Costs of Familial Intellectual Disability. International Journal of Environmental Research and Public Health. 21(3). 299–299. 1 indexed citations

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

Schofield, Deborah, Owen Tan, Rupendra Shrestha, et al.. (2020). IDMOD: An Australian microsimulation model of lifetime economic and social factors in familial intellectual disability. 13(1). 52–66. 2 indexed citations

Wiley, Veronica, Bruce Bennetts, Louise Christie, et al.. (2018). Are We Ready for Fragile X Newborn Screening Testing?—Lessons Learnt from a Feasibility Study. International Journal of Neonatal Screening. 4(1). 9–9. 4 indexed citations

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

Kraan, Claudine M., Minh Bui, Alison D. Archibald, et al.. (2018). FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts. Genetics in Medicine. 20(12). 1627–1634. 19 indexed citations

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

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

Delatycki, Martin B., Jo Burke, Louise Christie, et al.. (2014). Human Genetics Society of Australasia Position Statement: Population-Based Carrier Screening for Cystic Fibrosis. Twin Research and Human Genetics. 17(6). 578–583. 15 indexed citations

10.

Christie, Louise, Bruce Bennetts, Veronica Wiley, et al.. (2013). Maternal attitudes to newborn screening for fragile X syndrome. American Journal of Medical Genetics Part A. 161(2). 301–311. 25 indexed citations

11.

Field, Michael, Ingrid E. Scheffer, Deepak Gill, et al.. (2012). Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations. European Journal of Human Genetics. 20(7). 806–809. 41 indexed citations

12.

Ronan, Anne, et al.. (2009). Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region. BMJ Case Reports. 2009. bcr0520091914–bcr0520091914. 14 indexed citations

13.

Christie, Louise, et al.. (2009). Outcomes of a cystic fibrosis carrier testing clinic for couples. The Medical Journal of Australia. 191(9). 499–501. 9 indexed citations

14.

Ullmann, Reinhard, Gillian Turner, Maria Kirchhoff, et al.. (2007). Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation. 28(7). 674–682. 204 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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