Shanaz Pasha

2.7k citations

14 papers · 919 indexed · h-index 14

Genetics top 10%
- Genetic Syndromes and Imprinting 2
Cell Biology top 10%
Molecular Biology
- RNA regulation and disease 3
- Connexins and lens biology 3
- Heat shock proteins research 2
- Hedgehog Signaling Pathway Studies 1
Aging
Cellular and Molecular Neuroscience top 10%
Pediatrics, Perinatology and Child Health
- Neonatal and fetal brain pathology 1
Psychiatry and Mental health
- Child Nutrition and Feeding Issues 1
Surgery
- Eosinophilic Esophagitis 1

Co-authors: Eamonn R. Maher Esther Meyer Louise Tee Neil V. Morgan Richard C. Trembath Fatimah Rahman Colin A. Johnson C. Geoffrey Woods
Cited by: Genetics Cell Biology Molecular Biology
Journals: Journal of Clinical Investigation (2 papers)Brain (1 paper)The American Journal of Human Genetics (3 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

Shanaz Pasha

14 papers receiving 899 citations

Peers

Replace Shamir Zenvirt with:

Shamir Zenvirt Israel

Neil Dear United Kingdom

Louise Tee United Kingdom

Agnès Guichet France

Chaim Jalas United States

Tomohide Goto Japan

Elly Verbeek Netherlands

Jessica A. Panzer United States

Beverly A. Karpinski United States

Brice Marcet France

Shanaz Pasha relative to Shamir Zenvirt Israel Shamir Zenvirt's profile →

Citations per field

00.5×1.5×1.9×

Shamir Zenvirt · 1×

×0.8 295/367

GENET

×0.8 141/173

CB

×0.8 515/618

MB

×1.9 13/7

AGING

×0.6 128/205

CMN

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Countries citing papers authored by Shanaz Pasha

Since Specialization

Citations

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

Fields of papers citing papers by Shanaz Pasha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Shanaz Pasha, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Shanaz Pasha Line = papers co-authored together Shanaz Pasha links everyone, so they are left out of the graph.

All Works

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14 of 14 papers shown

#	Work
1	A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver disease Orphanet Journal of Rare Diseases ·Neil V. Morgan,Jane Hartley,Kenneth D.R. Setchell,Michael A. Simpson,Rachel E. Brown,Louise Tee,Sian Kirkham,Shanaz Pasha,Richard C. Trembath,Eamonn R. Maher,Paul Gissen,Déirdre Kelly	2013	17
2	Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease Molecular Genetics and Metabolism ·Esther Meyer,Manju A. Kurian,Neil V. Morgan,A. McNeill,Shanaz Pasha,Louise Tee,R. Younis,Andrew Norman,Marjo S. van der Knaap,Evangeline Wassmer,Richard C. Trembath,L A Brueton,Eamonn R. Maher	2011	18
3	Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells Journal of Clinical Investigation ·Neil V. Morgan,Sarah Goddard,Tony S. Cardno,David McDonald,Fatimah Rahman,D Barge,A. Ciupek,Anna Straatman-Iwanowska,Shanaz Pasha,Mary Guckian,Graham Anderson,Aarnoud Huissoon,Andrew J. Cant,Warren P. Tate,Sophie Hambleton,Eamonn R. Maher	2011	55
4	Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome) The American Journal of Human Genetics ·Esther Meyer,Christopher J. Ricketts,Neil V. Morgan,Mark R. Morris,Shanaz Pasha,Louise Tee,Fatimah Rahman,Anne Bazin,Bettina Bessières,Pierre Déchelotte,Mohamed Taher Yacoubi,Mudher Al‐Adnani,Tamás Marton,David Tannahill,Richard C. Trembath,Catherine Fallet‐Bianco,P. Cox,Denise Williams,Eamonn R. Maher	2010	46
5	Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathy Brain ·Manju A. Kurian,Esther Meyer,Grace Vassallo,Neil V. Morgan,Nandhini Prakash,Shanaz Pasha,Nebula A. Hai,Salwati Shuib,Fatima Rahman,Evangeline Wassmer,J. Helen Cross,Finbar O’Callaghan,John Osborne,Ingrid E. Scheffer,Paul Gissen,Eamonn R. Maher	2010	78
6	Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy. PubMed ·Esther Meyer,Michel Michaelides,Louise Tee,Anthony G. Robson,Fatimah Rahman,Shanaz Pasha,Linda Luxon,Anthony T. Moore,Eamonn R. Maher	2010	39
7	Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia Journal of Clinical Investigation ·Manju A. Kurian,Juan Zhen,Shuyuan Cheng,Yan Li,Santosh Mordekar,Philip Jardine,Neil V. Morgan,Esther Meyer,Louise Tee,Shanaz Pasha,Evangeline Wassmer,Simon Heales,Paul Gissen,Maarten E. A. Reith,Eamonn R. Maher	2009	148
8	Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) PLoS Genetics ·Esther Meyer,Derek Lim,Shanaz Pasha,Louise Tee,Fatimah Rahman,John R.W. Yates,C. Geoffrey Woods,Wolf Reik,Eamonn R. Maher	2009	183
9	A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption Molecular Genetics and Metabolism ·Esther Meyer,Manju A. Kurian,Shanaz Pasha,Richard C. Trembath,Trevor Cole,Eamonn R. Maher	2009	25
10	Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract. PubMed ·Esther Meyer,Fatimah Rahman,Jessica H. Owens,Shanaz Pasha,Neil V. Morgan,Richard C. Trembath,Edwin M. Stone,Anthony T. Moore,Eamonn R. Maher	2009	24
11	Autozygosity mapping of Bardet–Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10 European Journal of Human Genetics ·Dominic R A White,Anuradha Ganesh,Darryl Nishimura,Eleanor Rattenberry,Shakeel Ahmed,Ursula M. Smith,Shanaz Pasha,Sandy Raeburn,Richard C. Trembath,Anna Rajab,Fiona MacDonald,Eyal Banin,Edwin M. Stone,Colin A. Johnson,Val C. Sheffield,Eamonn R. Maher	2006	22
12	Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome The American Journal of Human Genetics ·Neil V. Morgan,Louise Brueton,P. Cox,Marie T. Greally,John Tolmie,Shanaz Pasha,Irene A. Aligianis,Hans van Bokhoven,Tamás Marton,Lihadh Al‐Gazali,Jenny E.V. Morton,Christine Oley,Colin A. Johnson,Richard C. Trembath,Han G. Brunner,Eamonn R. Maher	2006	98
13	Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations Human Genetics ·Tim Forshew,Colin A. Johnson,Shagufta Khaliq,Shanaz Pasha,Catherine Willis,Rashida Abbasi,Louise Tee,Ursula M. Smith,Richard C. Trembath,S. Qasim Mehdi,Anthony T. Moore,Eamonn R. Maher	2005	66
14	A Germline Mutation in BLOC1S3/Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8) The American Journal of Human Genetics ·Neil V. Morgan,Shanaz Pasha,Colin A. Johnson,John R. Ainsworth,Robin A.J. Eady,Ban B. Dawood,C McKeown,Richard C. Trembath,Jonathan T. Wilde,Steve P. Watson,Eamonn R. Maher	2005	100

About Shanaz Pasha

Shanaz Pasha is a scholar working on Cellular and Molecular Neuroscience, Sensory Systems and Cell Biology, having authored 14 papers that have together received 919 indexed citations. Recurring topics across this work include RNA regulation and disease (3 papers), Connexins and lens biology (3 papers), Genetic Syndromes and Imprinting (2 papers), Heat shock proteins research (2 papers), Neonatal and fetal brain pathology (1 paper), Child Nutrition and Feeding Issues (1 paper), Hedgehog Signaling Pathway Studies (1 paper) and Eosinophilic Esophagitis (1 paper). The work is most often cited by research in Genetics (295 citations), Cell Biology (141 citations) and Molecular Biology (515 citations). Shanaz Pasha has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Eamonn R. Maher, Esther Meyer, Louise Tee, Neil V. Morgan, Richard C. Trembath, Fatimah Rahman, Colin A. Johnson, C. Geoffrey Woods, John R.W. Yates and Wolf Reik. Their work appears in journals such as Journal of Clinical Investigation, Brain and The American Journal of Human 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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