Louise H. Williams

615 total citations
15 papers, 504 citations indexed

About

Louise H. Williams is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Louise H. Williams has authored 15 papers receiving a total of 504 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Sensory Systems and 5 papers in Genetics. Recurrent topics in Louise H. Williams's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Cancer Genomics and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Louise H. Williams is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Cancer Genomics and Diagnostics (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Louise H. Williams collaborates with scholars based in Australia, United States and Japan. Louise H. Williams's co-authors include Ian Campbell, Manasa Ramakrishna, Anita Sridhar, Kylie L. Gorringe, Samantha E. Boyle, Shehnaaz S.M. Manji, Kerry A. Miller, Hans‐Henrik M. Dahl, Terence P. Speed and Sandra Johnson and has published in prestigious journals such as PLoS ONE, Oncogene and Clinical Cancer Research.

In The Last Decade

Louise H. Williams

15 papers receiving 498 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Louise H. Williams Australia	13	333	138	90	67	67	15	504
H. Helen Lin United States	18	587 1.8×	251 1.8×	140 1.6×	33 0.5×	39 0.6×	24	839
Erica Bussani Italy	10	479 1.4×	34 0.2×	20 0.2×	61 0.9×	34 0.5×	12	560
Mathieu Quinodoz Switzerland	15	419 1.3×	75 0.5×	47 0.5×	14 0.2×	220 3.3×	40	622
Kaori Ushida Japan	12	298 0.9×	85 0.6×	132 1.5×	17 0.3×	52 0.8×	24	501
Dawid Eckert Germany	6	520 1.6×	55 0.4×	56 0.6×	7 0.1×	150 2.2×	7	655
Avni Santani United States	16	405 1.2×	110 0.8×	26 0.3×	21 0.3×	439 6.6×	39	781
Rhodora Gacayan United States	8	575 1.7×	61 0.4×	126 1.4×	8 0.1×	281 4.2×	8	850
Marc Munnes Germany	9	207 0.6×	139 1.0×	113 1.3×	10 0.1×	71 1.1×	11	403
Ashley C. Kramer United States	13	490 1.5×	58 0.4×	36 0.4×	40 0.6×	75 1.1×	28	653
Michel V. Hadjihannas Germany	13	585 1.8×	78 0.6×	98 1.1×	10 0.1×	80 1.2×	14	686

Countries citing papers authored by Louise H. Williams

Since Specialization

Citations

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

Fields of papers citing papers by Louise H. Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise H. Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Louise H. Williams. A scholar is included among the top collaborators of Louise H. Williams 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 H. Williams. Louise H. Williams 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:

15 of 15 papers shown

Miller, Kerry A., Louise H. Williams, Hans‐Henrik M. Dahl, & Shehnaaz S.M. Manji. (2013). Eeyore: A Novel Mouse Model of Hereditary Deafness. PLoS ONE. 8(9). e74243–e74243. 1 indexed citations

Williams, Louise H., Kerry A. Miller, Hans‐Henrik M. Dahl, & Shehnaaz S.M. Manji. (2013). Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction. Hearing Research. 299. 53–62. 15 indexed citations

Manji, Shehnaaz S.M., Kerry A. Miller, Louise H. Williams, & Hans‐Henrik M. Dahl. (2012). Identification of Three Novel Hearing Loss Mouse Strains with Mutations in the Tmc1 Gene. American Journal Of Pathology. 180(4). 1560–1569. 30 indexed citations

Miller, Kerry A., Louise H. Williams, Elizabeth Rose, et al.. (2012). Inner Ear Morphology Is Perturbed in Two Novel Mouse Models of Recessive Deafness. PLoS ONE. 7(12). e51284–e51284. 9 indexed citations

Manji, Shehnaaz S.M., Louise H. Williams, Kerry A. Miller, et al.. (2011). A Mutation in Synaptojanin 2 Causes Progressive Hearing Loss in the ENU-Mutagenised Mouse Strain Mozart. PLoS ONE. 6(3). e17607–e17607. 36 indexed citations

Manji, Shehnaaz S.M., Kerry A. Miller, Louise H. Williams, et al.. (2011). An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice. American Journal Of Pathology. 179(2). 903–914. 23 indexed citations

Ramakrishna, Manasa, Louise H. Williams, Samantha E. Boyle, et al.. (2010). Identification of Candidate Growth Promoting Genes in Ovarian Cancer through Integrated Copy Number and Expression Analysis. PLoS ONE. 5(4). e9983–e9983. 101 indexed citations

Ching, Michael S., et al.. (2010). Stability of Intravenous Flucloxacillin Solutions used for Hospital‐in‐the‐Home. Journal of Pharmacy Practice and Research. 40(2). 101–105. 12 indexed citations

Gorringe, Kylie L., Joshy George, Michael S. Anglesio, et al.. (2010). Copy Number Analysis Identifies Novel Interactions Between Genomic Loci in Ovarian Cancer. PLoS ONE. 5(9). e11408–e11408. 71 indexed citations

10.

Gorringe, Kylie L., Manasa Ramakrishna, Louise H. Williams, et al.. (2009). Are there any more ovarian tumor suppressor genes? A new perspective using ultra high‐resolution copy number and loss of heterozygosity analysis. Genes Chromosomes and Cancer. 48(10). 931–942. 53 indexed citations

11.

Gorringe, Kylie L., David Y.H. Choong, Louise H. Williams, et al.. (2008). Mutation and Methylation Analysis of the Chromodomain-Helicase-DNA Binding 5 Gene in Ovarian Cancer. Neoplasia. 10(11). 1253–IN32. 67 indexed citations

12.

Liu, Mira C.P., et al.. (2006). Genetic and epigenetic analysis of the TIMP-3 gene in ovarian cancer. Cancer Letters. 247(1). 91–97. 13 indexed citations

13.

Blancher, Christine, Wen Qiu, Ingrid Revet, et al.. (2006). ST7-mediated suppression of tumorigenicity of prostate cancer cells is characterized by remodeling of the extracellular matrix. Oncogene. 25(28). 3924–3933. 18 indexed citations

14.

Williams, Louise H., et al.. (2006). Genetic and Epigenetic Analysis of CHEK2 in Sporadic Breast, Colon, and Ovarian Cancers. Clinical Cancer Research. 12(23). 6967–6972. 43 indexed citations

15.

Williams, Louise H., Peter J. McClive, Jocelyn A. van den Bergen, & Andrew Sinclair. (2005). Annexin XI co‐localises with calcyclin in proliferating cells of the embryonic mouse testis. Developmental Dynamics. 234(2). 432–437. 12 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