May Tassabehji

3.9k total citations
38 papers, 1.6k citations indexed

About

May Tassabehji is a scholar working on Developmental Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, May Tassabehji has authored 38 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Developmental Neuroscience, 14 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in May Tassabehji's work include Williams Syndrome Research (16 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (3 papers). May Tassabehji is often cited by papers focused on Williams Syndrome Research (16 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (3 papers). May Tassabehji collaborates with scholars based in United Kingdom, United States and Australia. May Tassabehji's co-authors include Andy Brass, Annette Karmiloff‐Smith, Dian Donnai, Andrew Read, Jill Clayton‐Smith, Kay Metcalfe, Michael A. Patton, Tom Strachan, Ana Beleza‐Meireles and Jorge Saraiva and has published in prestigious journals such as Science, Nature Communications and Nature Genetics.

In The Last Decade

May Tassabehji

37 papers receiving 1.6k citations

Peers

Countries citing papers authored by May Tassabehji

Since Specialization

Citations

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

Fields of papers citing papers by May Tassabehji

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of May Tassabehji

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Hardy-Weinberg Equilibrium in the Large Scale Genomic Sequencing Era 2020 ·Frontiers in Genetics ·(unknown), Andy Brass, May Tassabehji	56
2	Ancestry of the AUTS2 family–A novel group of polycomb-complex proteins involved in human neurological disease 2020 ·PLoS ONE ·(unknown), David L. Robertson, May Tassabehji	8
3	GeVIR is a continuous gene-level metric that uses variant distribution patterns to prioritize disease candidate genes 2019 ·Nature Genetics ·(unknown), Andy Brass, May Tassabehji	20
4	Opposite effects on facial morphology due to gene dosage sensitivity 2014 ·Human Genetics ·Peter Hammond, Shane McKee, Michael Suttie, Judith Allanson, Jan-Maarten Cobben, Saskia M. Maas, Oliver Quarrell, Ann C. M. Smith, M. E. Suzanne Lewis, May Tassabehji, Sanjay M. Sisodiya, Teresa Mattina, Raoul C. M. Hennekam	11
5	A Role for Transcription Factor GTF2IRD2 in Executive Function in Williams-Beuren Syndrome 2012 ·PLoS ONE ·Melanie Porter, Carol Dobson‐Stone, John B. Kwok, Peter R. Schofield, William S. Beckett, May Tassabehji	35
6	Social Cognition in Williams Syndrome: Genotype/Phenotype Insights from Partial Deletion Patients 2012 ·Frontiers in Psychology ·Annette Karmiloff‐Smith, Hannah Broadbent, Emily K. Farran, Elena Vittoria Longhi, Dean D’Souza, Kay Metcalfe, May Tassabehji, Rachel Wu, Atsushi Senju, Francesca Happé, Peter D. Turnpenny, Francis H. Sansbury	37
7	Genome-Wide High-Resolution Screening in Dupuytren's Disease Reveals Common Regions of DNA Copy Number Alterations 2010 ·The Journal Of Hand Surgery ·Barbara Shih, May Tassabehji, (unknown), (unknown), Ardeshir Bayat	7
8	Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome 2008 ·Human Mutation ·May Tassabehji, Zhi Fang, Emma Hilton, Julie McGaughran, Zhongming Zhao, Charles E. de Bock, Emma Howard, (unknown), Dian Donnai, Ashish D. Diwan, Forbes Manson, (unknown), Raymond A. Clarke	148
9	A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome 2008 ·Clinical Genetics ·Richard O. Day, (unknown), Dian Donnai, Alan Fryer, (unknown), Peter Howard, Bronwyn Kerr, Sahar Mansour, Una Maye, Shane McKee, Shehla Mohammed, Elizabeth Sweeney, May Tassabehji, (unknown), Jill Clayton‐Smith	17
10	Geroderma osteodysplastica maps to a 4 Mb locus on chromosome 1q24 2008 ·American Journal of Medical Genetics Part A ·William G. Newman, Jill Clayton‐Smith, Kay Metcalfe, (unknown), Marco Tartaglia, Francesco Brancati, (unknown), Antonio Novelli, Xiangdong Liu, Katherine Siminovitch, Stefan Mundlos, May Tassabehji, Graeme C. Black	8
11	GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif ‘GUCE’ 2007 ·FEBS Letters ·Pamela Thompson, Michelle Webb, William S. Beckett, (unknown), Thomas A. Jowitt, Andrew D Sharrocks, May Tassabehji	15
12	Congenital Heart Disease: Molecular Diagnostics of Supravalvular Aortic Stenosis 2006 ·Congenital Heart Disease ·May Tassabehji, Zsolt Urbán	9
13	GTF2IRD1 in Craniofacial Development of Humans and Mice 2005 ·Science ·May Tassabehji, Peter Hammond, Annette Karmiloff‐Smith, Pamela Thompson, Snorri S. Thorgeirsson, Marian E. Durkin, Nicholas C. Popescu, (unknown), Kay Metcalfe, (unknown), Helen Stewart, Andrew Read, Mark Maconochie, Dian Donnai	145
14	Discriminating Power of Localized Three-Dimensional Facial Morphology 2005 ·The American Journal of Human Genetics ·Peter Hammond, Tim J. Hutton, Judith Allanson, Bernard Buxton, Linda Campbell, Jill Clayton‐Smith, Dian Donnai, Annette Karmiloff‐Smith, Kay Metcalfe, Kieran C. Murphy, Michael A. Patton, Barbara R. Pober, Katrina Prescott, Peter Scambler, Adam Shaw, Ann C. M. Smith, Angela Stevens, I. Karen Temple, Raoul C. M. Hennekam, May Tassabehji	118
15	Exploring Williams–Beuren syndrome using myGrid 2004 ·Bioinformatics ·Robert Stevens, Hannah Tipney, Chris Wroe, Tom Oinn, Martin Senger, Phillip Lord, Carole Goble, Andy Brass, May Tassabehji	75
16	Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams–Beuren syndrome 2004 ·European Journal of Human Genetics ·Hannah Tipney, (unknown), Andy Brass, Kay Metcalfe, Dian Donnai, May Tassabehji	45
17	Comparison of TFII‐I gene family members deleted in Williams‐Beuren syndrome 2004 ·Protein Science ·(unknown), (unknown), Hannah Tipney, Andy Brass, May Tassabehji	38
18	Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis 1997 ·Human Molecular Genetics ·May Tassabehji	118
19	Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes 1996 ·Human Mutation ·David J. Hughes, Andrew J. Wallace, Joanne Taylor, May Tassabehji, (unknown), Alison Hill, N. C. Nevin, Colin A. Graham	8
20	A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency. 1992 ·Genome Research ·Simon Collier, May Tassabehji, T Strachan	8

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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