Niolette I. McGill

1.8k total citations
7 papers, 1.4k citations indexed

About

Niolette I. McGill is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Niolette I. McGill has authored 7 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Genetics. Recurrent topics in Niolette I. McGill's work include Ocular Disorders and Treatments (3 papers), CRISPR and Genetic Engineering (2 papers) and Chromosomal and Genetic Variations (2 papers). Niolette I. McGill is often cited by papers focused on Ocular Disorders and Treatments (3 papers), CRISPR and Genetic Engineering (2 papers) and Chromosomal and Genetic Variations (2 papers). Niolette I. McGill collaborates with scholars based in United Kingdom, Australia and Japan. Niolette I. McGill's co-authors include Howard J. Cooke, Janet C. Lindsey, Daryll K. Green, David Fitzpatrick, Judy Fantes, Veronica van Heyningen, Brenda R. Grimes, Megumi Nakano, Kaori Saitoh and Tuneko Okazaki and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Nature Biotechnology.

In The Last Decade

Niolette I. McGill

7 papers receiving 1.4k citations

Peers

Countries citing papers authored by Niolette I. McGill

Since Specialization

Citations

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

Fields of papers citing papers by Niolette I. McGill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Niolette I. McGill. 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 Niolette I. McGill. The network helps show where Niolette I. McGill may publish in the future.

Co-authorship network of co-authors of Niolette I. McGill

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome 2006 ·Human Molecular Genetics ·Kathleen A. Williamson, Ann Hever, Joe Rainger, R. Curtis Rogers, Alex Magee, (unknown), Wee Teik Keng, Freddie H. Sharkey, Niolette I. McGill, (unknown), Adele Schneider, Mario Messina, Peter D. Turnpenny, Judy Fantes, Veronica van Heyningen, David Fitzpatrick	158
2	Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome 2006 ·Human Molecular Genetics ·Kathleen A. Williamson, Ann Hever, Joe Rainger, R. Curtis Rogers, Alex Magee, (unknown), Wee Teik Keng, Freddie H. Sharkey, Niolette I. McGill, (unknown), Adele Schneider, Mario Messina, Peter D. Turnpenny, Judy Fantes, Veronica van Heyningen, David Fitzpatrick	7
3	MLYCD mutation analysis: Evidence for protein mistargeting as a cause of MLYCD deficiency 2003 ·Human Mutation ·(unknown), René Santer, Antònia Ribes, Frances Dougherty, Niolette I. McGill, David R. Thorburn, David Fitzpatrick	36
4	Mutations in SOX2 cause anophthalmia 2003 ·Nature Genetics ·Judy Fantes, Nicola Ragge, Sally Ann Lynch, Niolette I. McGill, J. R. O. Collin, Patricia N. Howard‐Peebles, Caroline Hayward, Anthony J. Vivian, Kathy Williamson, Veronica van Heyningen, David Fitzpatrick	403
5	Construction of YAC–based mammalian artificial chromosomes 1998 ·Nature Biotechnology ·Masashi Ikeno, Brenda R. Grimes, Tuneko Okazaki, Megumi Nakano, Kaori Saitoh, (unknown), Niolette I. McGill, Howard J. Cooke, Hiroshi Masumoto	356
6	In vivo loss of telomeric repeats with age in humans 1991 ·Mutation Research/DNAging ·Janet C. Lindsey, Niolette I. McGill, (unknown), Daryll K. Green, Howard J. Cooke	378
7	The structure of a subterminal repeated sequence present on many human chromosomes 1990 ·Nucleic Acids Research ·Sally H. Cross, Janet C. Lindsey, Judith A. Fantes, (unknown), Niolette I. McGill, Howard J. Cooke	89

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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