Fathimath Faiz

571 total citations
13 papers, 116 citations indexed

About

Fathimath Faiz is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Fathimath Faiz has authored 13 papers receiving a total of 116 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Surgery. Recurrent topics in Fathimath Faiz's work include Genetic factors in colorectal cancer (4 papers), Lipoproteins and Cardiovascular Health (4 papers) and Genomics and Rare Diseases (3 papers). Fathimath Faiz is often cited by papers focused on Genetic factors in colorectal cancer (4 papers), Lipoproteins and Cardiovascular Health (4 papers) and Genomics and Rare Diseases (3 papers). Fathimath Faiz collaborates with scholars based in Australia, Spain and Malaysia. Fathimath Faiz's co-authors include Amanda J. Hooper, Frank M. van Bockxmeer, Richard Allcock, Phillipa J. Lamont, C. Wise, Nigel G. Laing, Macarena Cabrera‐Serrano, Gianina Ravenscroft, Jordan Boutilier and Mark R. Davis and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics and Atherosclerosis.

In The Last Decade

Fathimath Faiz

12 papers receiving 104 citations

Peers

Countries citing papers authored by Fathimath Faiz

Since Specialization

Citations

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

Fields of papers citing papers by Fathimath Faiz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fathimath Faiz

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	A KLHL40 3’ UTR splice-altering variant causes milder NEM8, an under-appreciated disease mechanism 2022 ·Human Molecular Genetics ·(unknown), (unknown), Emilia Servián‐Morilla, Eloy Rivas, Fathimath Faiz, Patricia A. Sullivan, Emily C. Oates, Joshua S. Clayton, Rhonda L. Taylor, Mark R. Davis, Traude H. Beilharz, Nigel G. Laing, Macarena Cabrera‐Serrano, Gianina Ravenscroft	7
2	CONGENITAL MYOPATHIES – NEMALINE MYOPATHIES 2021 ·Neuromuscular Disorders ·(unknown), Fathimath Faiz, Emilia Servián‐Morilla, Eloy Rivas, Patricia A. Sullivan, Emily C. Oates, Joshua S. Clayton, Rhonda L. Taylor, Mark R. Davis, Nigel G. Laing, Macarena Cabrera‐Serrano, Gianina Ravenscroft	2
3	Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate 2020 ·Human Mutation ·Lauren Akesson, Adam Bournazos, Andrew Fennell, Emma Krzesinski, Kenneth Tan, Amanda Springer, Katherine Rose, Ilias Goranitis, David Francis, (unknown), Fathimath Faiz, Mark R. Davis, John Christodoulou, Sebastian Lunke, Zornitza Stark, Matthew F. Hunter, Sandra T. Cooper	8
4	Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience 2020 ·Annals of Clinical and Translational Neurology ·Sarah J. Beecroft, Kyle S. Yau, Richard J. N. Allcock, Kym Mina, Rebecca Gooding, Fathimath Faiz, (unknown), C. Wise, Padma Sivadorai, (unknown), Nina Kresoje, Royston Ong, Rachael M. Duff, Macarena Cabrera‐Serrano, Kristen L. Nowak, Nicholas Pachter, Gianina Ravenscroft, Phillipa J. Lamont, Mark R. Davis, Nigel G. Laing	24
5	P.231Paternal uniparental disomy of chromosome 19 unmasking a recessive variant in RYR1 in a case of congenital core myopathy with additional features 2019 ·Neuromuscular Disorders ·Mark R. Davis, Fathimath Faiz, (unknown), Joshua S. Clayton, Thomas Robertson, Dimitar N. Azmanov, Anita Cairns	0
6	Adult onset distal and proximal myopathy with complete ophthalmoplegia associated with a novel de novo p.(Leu1877Pro) mutation in MYH2 2014 ·Clinical Genetics ·Macarena Cabrera‐Serrano, (unknown), Jordan Boutilier, C. Wise, Fathimath Faiz, Phillipa J. Lamont, Nigel G. Laing	11
7	Molecular characterization of a Chinese woman homozygous for the familial hypercholesterolemia LDLR c.1474G>A (p.Asp492Asn) mutation 2014 ·Clinical Lipidology ·Fathimath Faiz, Miao Hu, Amanda J. Hooper, Brian Tomlinson, Frank M. van Bockxmeer	1
8	Genetic screening to improve the diagnosis of familial hypercholesterolemia 2014 ·Clinical Lipidology ·Fathimath Faiz, Lan Nguyen, Frank M. van Bockxmeer, Amanda J. Hooper	1
9	Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing 2013 ·Atherosclerosis ·Fathimath Faiz, Richard Allcock, Amanda J. Hooper, Frank M. van Bockxmeer	17
10	Targeted RNAi of the mitogen-activated protein kinase pathway genes in acute myeloid leukemia cells 2013 ·(unknown), (unknown), Fathimath Faiz, (unknown)	3
11	Molecular pathology of familial hypercholesterolemia, related dyslipidemias and therapies beyond the statins 2012 ·Critical Reviews in Clinical Laboratory Sciences ·Fathimath Faiz, Amanda J. Hooper, Frank M. van Bockxmeer	15
12	Smad2:A Candidate Gene for the Murine Autoimmune Diabetes LocusIdd21.1 2011 ·The Journal of Clinical Endocrinology & Metabolism ·Sarah Hook, Amanda Phipps‐Green, Fathimath Faiz, (unknown), Cushla McKinney, Jade E. Hollis‐Moffatt, Tony R. Merriman	4
13	Isolation, screening and development of local bacterial consortia with azo dyes decolourising capability 2009 ·Malaysian Journal of Microbiology ·(unknown), (unknown), Fathimath Faiz	23

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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