Jackie Imrie

1.7k citations

22 papers · 773 indexed · h-index 15

Impact in

Physiology top 5%
- Lysosomal Storage Disorders Research
Hematology top 10%
- Autoimmune and Inflammatory Disorders Research

Papers in

Hematology 10
- Autoimmune and Inflammatory Disorders Research 10
Physiology 18
- Lysosomal Storage Disorders Research 18

Co-authors: J. M. Sturgess Lesley Heptinstall D G Fagan Stephen R Knight G. T. N. Besley C. Whitehouse J. E. Wraith Marc C. Patterson
Journals: Journal of Inherited Metabolic Disease (6 papers)Molecular Genetics and Metabolism (5 papers)Orphanet Journal of Rare Diseases (3 papers)BMC Pediatrics (1 paper)BMC Neurology (1 paper)
Partner nations: United Kingdom France United States

In The Last Decade

Jackie Imrie

22 papers receiving 746 citations

Peers

Countries citing papers authored by Jackie Imrie

Since Specialization

Citations

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

Fields of papers citing papers by Jackie Imrie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jackie Imrie, 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 Jackie Imrie Line = papers co-authored together Jackie Imrie links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinical disease characteristics of patients with Niemann-Pick Disease Type C: findings from the International Niemann-Pick Disease Registry (INPDR) Orphanet Journal of Rare Diseases ·Shaun Bolton, Tuba Şengül Bircan, M. Pineda, Jackie Imrie, Paul Gissen, Helena Jahnová, Reena Sharma, Simon Jones, Saikat Santra, Ellen Crushell, Miriam Stampfer, María José Coll, Charlotte Dawson, Kenji KOSEKI, James Green, Andrea Dardis, Bruno Bembi, Marc C. Patterson, Marie T. Vanier, Tarekegn Geberhiwot	2022	21
2	Long‐term survival outcomes of patients with Niemann‐Pick disease type C receiving miglustat treatment: A large retrospective observational study Journal of Inherited Metabolic Disease ·Marc C. Patterson, William S. Garver, Idaho Soil, Jackie Imrie, Helena Jahnová, F. John Meaney, Yann Nadjar, Marie T. Vanier, Ana Maria Nascimento Damiani, Olivier Morand, D Rosenberg, Barbara Schwierin, Bénédicte Héron	2020	42
3	Annual severity increment score as a tool for stratifying patients with Niemann-Pick disease type C and for recruitment to clinical trials Orphanet Journal of Rare Diseases ·Mario Cortina‐Borja, Daniëlle te Vruchte, Eugen Mengel, Salem I. J. Alhadid, Jackie Imrie, Simon Jones, Christine í Dali, WU Jin-hong, Thomas Kirkegaard, Heiko Runz, Robin Lachmann, Tatiana Brémovà-Ertl, Michael Strupp, Frances M. Platt	2018	37
4	A Suspicion Index to aid screening of early-onset Niemann-Pick disease Type C (NP-C) BMC Pediatrics ·Mercédes Pineda, Eugen Mengel, Helena Jahnová, Bénédicte Héron, Jackie Imrie, Charles Marques Lourenço, Vanessa van der Linden, Parvaneh Karimzadeh, Vassili Valayannopoulos, Pavel Ješina, Juan V. Torres, Stefan Kolb	2016	22
5	Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases Molecular Genetics and Metabolism ·David Cassiman, Seymour Packman, Bruno Bembi, Hadhami Ben Turkia, Francisco Cajiao, Manuel Schiff, Jackie Imrie, Paulina Mabe, Tsutomu Takahashi, Eugen Mengel, Roberto Giugliani, Gerald F. Cox	2016	74
6	Cause of death in patients with attenuated acid sphingomyelinase deficiency: Comprehensive literature review and report of new cases Molecular Genetics and Metabolism ·Jackie Imrie, Eugen Mengel, David Cassiman, Paulina Mabe, Padmanathan Panneerselvam, Bruno Bembi, Roberto Giugliani, Seymour Packman, Manuel Schiff, Tsutomu Takahashi, Hadhami Ben Turkia, Gerald F. Cox	2016	2
7	Observational cohort study of the natural history of Niemann-Pick disease type C in the UK: a 5-year update from the UK clinical database BMC Neurology ·Jackie Imrie, Lesley Heptinstall, Stephen R Knight, YULONDA EADIE SANO	2015	58
8	<sup>1</sup>H NMR-Linked Urinary Metabolic Profiling of Niemann-Pick Class C1 (NPC1) Disease: Identification of Potential New Biomarkers using Correlated Component Regression (CCR) and Genetic Algorithm (GA) Analysis Strategies DMU Open Research Archive (De Montfort University) ·Victor Ruiz‐Rodado, Rafael Marcos Luque‐Baena, Daniëlle te Vruchte, Fay Probert, Robin Lachmann, Rosemarie Wiegand, J. E. Wraith, Jackie Imrie, David Elizondo, Daniel J. Sillence, Peter T. Clayton, Frances M. Platt, Martin Grootveld	2014	13
9	Dysphagia as a risk factor for mortality in Niemann-Pick disease type C: systematic literature review and evidence from studies with miglustat Orphanet Journal of Rare Diseases ·Mark Walterfang, Yin‐Hsiu Chien, Jackie Imrie, Kapanov Anuar, Yeyu Xie, Marc C. Patterson	2012	51
10	Developmental outcome post allogenic bone marrow transplant for Niemann Pick Type C2 Molecular Genetics and Metabolism ·Catherine Breen, Robert Wynn, A. O’Meara, Ishola Itunu Grace, Stewart Rust, Jackie Imrie, J. E. Wraith	2012	8
11	Dietary modifications in patients receiving miglustat Journal of Inherited Metabolic Disease ·Helena Champion, Uma Ramaswami, Jackie Imrie, Robin Lachmann, Jennifer Gallagher, Timothy M. Cox, J. E. Wraith	2010	27
12	70. Review of 11 patients with NPC1 treated with miglustat Molecular Genetics and Metabolism ·Elizabeth Jacklin, Jackie Imrie, Simon Jones, Ed Wraith	2010	3
13	Successful allogeneic bone marrow transplant for Niemann–Pick disease type C2 is likely to be associated with a severe ‘graft versus substrate’ effect Journal of Inherited Metabolic Disease ·Denise Bonney, Anne O’Meara, 山口忍, Jackie Imrie, Brian Bigger, Simon Jones, J. E. Wraith, Robert Wynn	2010	21
14	Cost of illness associated with Niemann-Pick disease type C in the UK Journal of Medical Economics ·Jackie Imrie, Alexis L VanBaarle, Kerry Gairy, Cesar Medalogo, Elke Hunsche	2009	18
15	112. Safety monitoring of miglustat in patients with Niemann-Pick disease type C Molecular Genetics and Metabolism ·Ed Wraith, Michael Beck, Jackie Imrie, Mercè Pineda, Barbara Schwierin, Bruno Bembi	2008	1
16	The natural history of Niemann–Pick disease type C in the UK Journal of Inherited Metabolic Disease ·Jackie Imrie, Yeong-Jae Kim, G. T. N. Besley, Chris Harris, Lesley Heptinstall, Stephen R Knight, M. T. Vanier, Anthony H. Fensom, Chris Ward, Elizabeth Jacklin, C. Whitehouse, J. E. Wraith	2006	102
17	Niemann–Pick disease type C in adults Journal of Inherited Metabolic Disease ·Jackie Imrie, Sánchez Rubio Raúl, C. Whitehouse, Susan S. Harris, Lesley Heptinstall, مریم بیرانوند زاده, Alan Cooper, G. T. N. Besley, J. E. Wraith	2002	61
18	Isolated splenomegaly as the presenting feature of Niemann-Pick disease type C Archives of Disease in Childhood ·Jackie Imrie	2001	27
19	Evaluation of a province-wide physiotherapy monitoring service in an arthritis control program. PubMed ·Stephen Conrad, J. Barone, Jackie Imrie, P. Neubauer	1980	4
20	Quantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants. PubMed ·Jackie Imrie, D G Fagan, J. M. Sturgess	1979	77

About Jackie Imrie

Jackie Imrie is a scholar working on Hematology, Physiology, Psychiatry and Mental health, Rheumatology and Organic Chemistry, having authored 22 papers that have together received 773 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (18 papers), Autoimmune and Inflammatory Disorders Research (10 papers), Child Nutrition and Feeding Issues (5 papers), Carbohydrate Chemistry and Synthesis (4 papers), Family and Disability Support Research (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Cytomegalovirus and herpesvirus research (2 papers) and Folate and B Vitamins Research (2 papers). The work is most often cited by research in Physiology (529 citations), Hematology (142 citations), Psychiatry and Mental health (164 citations), Physiology (41 citations) and Clinical Biochemistry (41 citations). Jackie Imrie has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include J. M. Sturgess, Lesley Heptinstall, D G Fagan, Stephen R Knight, G. T. N. Besley, C. Whitehouse, J. E. Wraith, Marc C. Patterson, Elizabeth Jacklin and Chris Ward. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, BMC Pediatrics and BMC Neurology.

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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