Mayada Tassabehji

3.1k citations

17 papers · 2.2k indexed · 1 hit paper · h-index 15

Co-authors: Andrew Read Tom Strachan Valerie Newton R Harris Rudi Balling Peter Gruß Dian Donnai Kay Metcalfe
Topics: Williams Syndrome Research (7 papers)Congenital heart defects research (3 papers)melanin and skin pigmentation (2 papers)
Cited by: Developmental Neuroscience Sensory Systems Cell Biology
Journals: Nature Nucleic Acids Research Nature Genetics
Partner nations: United Kingdom Australia United States

In The Last Decade

Mayada Tassabehji

17 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

1992 543 citations Mayada Tassabehji, Andrew Read et al. Nature profile →

Peers

Countries citing papers authored by Mayada Tassabehji

Since Specialization

Citations

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

Fields of papers citing papers by Mayada Tassabehji

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mayada Tassabehji

This figure shows the co-authorship network connecting the top 25 collaborators of Mayada Tassabehji. A scholar is included among the top collaborators of Mayada 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 Mayada Tassabehji. Mayada 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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17 of 17 papers shown

#	Work	Indexed citations
1	Spectrum of arterial obstructions caused by one elastin gene point mutation 2003 ·European Journal of Pediatrics ·A. Koch,G. Buheitel,Michael Hofbeck,Anita Rauch,Cornelia Kraus,Mayada Tassabehji,H. Singer	5
2	Mutations in PAX1 may be associated with Klippel–Feil syndrome 2003 ·European Journal of Human Genetics ·Julie McGaughran,Andrew C. Oates,Dian Donnai,Andrew Read,Mayada Tassabehji	76
3	Elastin: mutational spectrum in supravalvular aortic stenosis 2000 ·European Journal of Human Genetics ·Kay Metcalfe,(unknown),Leslie Smoot,(unknown),(unknown),Pascal McKeown,Victoria Mok Siu,Anita Rauch,John Dean,N R Dennis,Ian O. Ellis,William Reardon,Cheryl Cytrynbaum,Lucy R. Osborne,John R.W. Yates,Andrew Read,Dian Donnai,Mayada Tassabehji	110
4	Williams Syndrome: Use of Chromosomal Microdeletions as a Tool to Dissect Cognitive and Physical Phenotypes 1999 ·The American Journal of Human Genetics ·Mayada Tassabehji,Kay Metcalfe,Annette Karmiloff‐Smith,(unknown),Julia D. Grant,N R Dennis,William Reardon,Miranda Splitt,Andrew Read,D Donnai	166
5	A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome 1999 ·European Journal of Human Genetics ·Mayada Tassabehji,(unknown),Carrie M. Wilmot,Dian Donnai,Andrew Read,Kay Metcalfe	31
6	A Complete Physical Contig and Partial Transcript Map of the Williams Syndrome Critical Region 1999 ·Genomics ·(unknown),(unknown),Kay Metcalfe,Dian Donnai,Andrew Read,Mayada Tassabehji	41
7	Novel Mutations in the 1α-Hydroxylase (P450c1) Gene in Three Families with Pseudovitamin D–Deficiency Rickets Resulting in Loss of Functional Enzyme Activity in Blood-Derived Macrophages 1999 ·Journal of Bone and Mineral Research ·S J Smith,(unknown),Jacqueline Berry,Michael Davies,(unknown),C R Paterson,(unknown),Mayada Tassabehji,(unknown),A.P. Mee,E.B. Mawer	57
8	Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin 1998 ·American Journal of Medical Genetics ·(unknown),V. Reid Sutton,Elizabeth Nickerson,James R. Lupski,Lorraine Potocki,Julie R. Korenberg,Frank Greenberg,Mayada Tassabehji,Lisa G. Shaffer	77
9	An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa 1998 ·Human Molecular Genetics ·Mayada Tassabehji	125
10	Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome) 1998 ·Clinical Dysmorphology ·Jeanne Amiel,Peter Watkin,Mayada Tassabehji,Andrew Read,Robin M. Winter	76
11	Novel and recurrent mutations in the neurofibromatosis type 1 (NF1) gene 1997 ·Human Mutation ·Judith A. Hudson,(unknown),Mayada Tassabehji,(unknown),Stéphanie Simon,M Super,Dian Donnai,Nalin Thakker	11
12	The mutational spectrum in Waardenburg syndrome 1995 ·Human Molecular Genetics ·Mayada Tassabehji,Valerie Newton,(unknown),Angela F. Brady,Dian Donnai,Małgorzata Krajewska‐Walasek,Victoria Murday,Andrew Norman,Ewa Obersztyn,William Reardon,(unknown),Richard C. Trembath,Peter Wieacker,(unknown),Robin Winter,Andrew Read	172
13	Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene cluster 1994 ·Nucleic Acids Research ·Mayada Tassabehji,Tom Strachan,Michael J. Anderson,R. Duncan Campbell,Simon Collier,Majlinda Lako	54
14	Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene 1994 ·Nature Genetics ·Mayada Tassabehji,(unknown),Andrew Read	499
15	A de novo pathological point mutation at the 21–hydroxylase locus: implications for gene conversion in the human genome 1993 ·Nature Genetics ·Simon Collier,Mayada Tassabehji,Tom Strachan	66
16	Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome. 1993 ·PubMed ·Mayada Tassabehji,T Strachan,Mike Sharland,Andrew Colley,Dian Donnai,R Harris,Nalin Thakker	65
17	Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box genebreakdown → 1992 ·Nature ·Mayada Tassabehji,Andrew Read,Valerie Newton,R Harris,Rudi Balling,Peter Gruß,Tom Strachan	543

About Mayada Tassabehji

Mayada Tassabehji is a scholar working on Developmental Neuroscience, Sensory Systems and Cell Biology, having authored 17 papers that have together received 2.2k indexed citations. Recurring topics across this work include Williams Syndrome Research (7 papers), Congenital heart defects research (3 papers) and melanin and skin pigmentation (2 papers). The work is most often cited by research in Developmental Neuroscience (336 citations), Sensory Systems (250 citations) and Cell Biology (600 citations). Mayada Tassabehji has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Andrew Read, Tom Strachan, Valerie Newton, R Harris, Rudi Balling, Peter Gruß, Dian Donnai, Kay Metcalfe, William Reardon and Simon Collier. Their work appears in journals such as Nature, Nucleic Acids Research and Nature Genetics.

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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