Malcolm F. Howard

824 total citations
5 papers, 162 citations indexed

About

Malcolm F. Howard is a scholar working on Molecular Biology, Cell Biology and Surgery. According to data from OpenAlex, Malcolm F. Howard has authored 5 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Cell Biology and 1 paper in Surgery. Recurrent topics in Malcolm F. Howard's work include RNA modifications and cancer (1 paper), Cancer Mechanisms and Therapy (1 paper) and Airway Management and Intubation Techniques (1 paper). Malcolm F. Howard is often cited by papers focused on RNA modifications and cancer (1 paper), Cancer Mechanisms and Therapy (1 paper) and Airway Management and Intubation Techniques (1 paper). Malcolm F. Howard collaborates with scholars based in United Kingdom, Austria and Japan. Malcolm F. Howard's co-authors include Jenny C. Taylor, Usha Kini, Alistair T. Pagnamenta, Niko Popitsch, Gerardine Quaghebeur, Samantha J.L. Knight, Sahar Mansour, P. Cox, Tamás Balla and Éva Wisniewski and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Malcolm F. Howard

5 papers receiving 161 citations

Peers

Countries citing papers authored by Malcolm F. Howard

Since Specialization

Citations

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

Fields of papers citing papers by Malcolm F. Howard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Malcolm F. Howard. 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 Malcolm F. Howard. The network helps show where Malcolm F. Howard may publish in the future.

Co-authorship network of co-authors of Malcolm F. Howard

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

All Works

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5 of 5 papers shown

#	Work	Indexed citations
1	Seven years on from the Canadian Airway Focus Group Difficult Airway Guidelines: an observational survey 2021 ·Canadian Journal of Anesthesia/Journal canadien d anesthésie ·Malcolm F. Howard, Ruediger Noppens, (unknown), Philip M. Jones, (unknown)	1
2	Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders 2017 ·European Journal of Human Genetics ·(unknown), Alistair T. Pagnamenta, Yoshiko Murakami, John Taylor, Consuelo Anzilotti, Malcolm F. Howard, (unknown), Diana Johnson, (unknown), Sahar Mansour, I. Karen Temple, (unknown), Elisabeth Rosser, Rachel Harrison, (unknown), Niko Popitsch, Taroh Kinoshita, Jenny C. Taylor, Usha Kini	48
3	Activation of an exonic splice‐donor site in exon 30 of CDK5RAP2 in a patient with severe microcephaly and pigmentary abnormalities 2016 ·Clinical Case Reports ·Alistair T. Pagnamenta, Malcolm F. Howard, Samantha J.L. Knight, David A. Keays, Gerardine Quaghebeur, Jenny C. Taylor, Usha Kini	9
4	Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome 2015 ·Journal of Medical Genetics ·(unknown), Alistair T. Pagnamenta, Moira Blyth, Sahar Mansour, Vivienne McConnell, Ikuyo Kou, Shiro Ikegawa, Yoshinori Tsurusaki, Naomichi Matsumoto, Adriana Lo‐Castro, Ghislaine Plessis, Beate Albrecht, Agatino Battaglia, Jenny C. Taylor, Malcolm F. Howard, David A. Keays, (unknown), Susanne J. Kühl, Usha Kini, Alisdair McNeill	53
5	Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis 2015 ·Human Molecular Genetics ·Alistair T. Pagnamenta, Malcolm F. Howard, Éva Wisniewski, Niko Popitsch, Samantha J.L. Knight, David A. Keays, Gerardine Quaghebeur, Helen Cox, P. Cox, Tamás Balla, Jenny C. Taylor, Usha Kini	51

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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