Christine í Dali

1.1k citations

28 papers · 532 indexed · h-index 14

Physiology top 10%
- Lysosomal Storage Disorders Research 21
Physiology top 10%
- Lysosomal Storage Disorders Research 21
Neurology
- Neuroinflammation and Neurodegeneration Mechanisms 2
Psychiatry and Mental health
- Cerebral Palsy and Movement Disorders 3
Clinical Biochemistry
Molecular Biology
- RNA regulation and disease 4
Epidemiology
- Trypanosoma species research and implications 4
Hematology
- Autoimmune and Inflammatory Disorders Research 3
Pediatrics, Perinatology and Child Health
- Neonatal and fetal brain pathology 2
Genetics
- Neurogenetic and Muscular Disorders Research 2

Co-authors: Allan M. Lund Ingeborg Krägeloh‐Mann Line Borgwardt Samuel Groeschel J. Fogh Morten Dunø Christiane Kehrer Margaret Wasilewski
Cited by: Physiology Neurology
Journals: Neurology (2 papers)Developmental Medicine & Child Neurology (1 paper)Orphanet Journal of Rare Diseases (3 papers)
Partner nations: Denmark Germany United States

In The Last Decade

Christine í Dali

28 papers receiving 521 citations

Peers

Countries citing papers authored by Christine í Dali

Since Specialization

Citations

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

Fields of papers citing papers by Christine í Dali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine í Dali. 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 Christine í Dali. The network helps show where Christine í Dali may publish in the future.

Co-authorship network

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Effects of sulfatide on peripheral nerves in metachromatic leukodystrophy Annals of Clinical and Translational Neurology ·Mohamed H. Farah,Christine í Dali,Samuel Groeschel,Mihai Moldovan,David Whiteman,C. J. Malanga,Ingeborg Krägeloh‐Mann,Jing Li,Norman W. Barton,Christian Krarup	2023	4
2	Impacts and Burden of Niemann pick Type-C: a patient and caregiver perspective Orphanet Journal of Rare Diseases ·Eugen Mengel,Marc C. Patterson,Michael Chladek,Christina Guldberg,Christine í Dali,Tara Symonds,Lucy Lloyd-Price,Toni Mathieson,Joslyn Crowe,Claire Burbridge	2021	6
3	Safety of intrathecal delivery of recombinant human arylsulfatase A in children with metachromatic leukodystrophy: Results from a phase 1/2 clinical trial Molecular Genetics and Metabolism ·Christine í Dali,Caroline Sevin,Ingeborg Krägeloh‐Mann,Roberto Giugliani,Norio Sakai,James X. Wu,Margaret Wasilewski	2020	46
4	Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 study Annals of Clinical and Translational Neurology ·Christine í Dali,Samuel Groeschel,Mihai Moldovan,Mohamed Farah,Ingeborg Krägeloh‐Mann,Margaret Wasilewski,Jing Li,Norman W. Barton,Christian Krarup	2020	14
5	Efficacy and safety of Velmanase alfa in the treatment of patients with alpha‐mannosidosis: results from the core and extension phase analysis of a phase III multicentre, double‐blind, randomised, placebo‐controlled trial Journal of Inherited Metabolic Disease ·Line Borgwardt,Nathalie Guffon,Yasmina Amraoui,Christine í Dali,Linda De Meırleır,Mercedes Gil‐Campos,Bénédicte Héron,Silvia Geraci,Diego Ardigò,Federica Cattaneo,J. Fogh,J. M. Hannerieke Van den Hout,Michael Beck,Simon Jones,Anna Tylki‐Szymańska,Ulla Haugsted,Allan M. Lund	2018	38
6	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,Yasmin Amraoui,Jackie Imrie,Simon Jones,Christine í Dali,Paul Fineran,Thomas Kirkegaard,Heiko Runz,Robin Lachmann,Tatiana Brémovà-Ertl,Michael Strupp,Frances M. Platt	2018	37
7	The ethical framework for performing research with rare inherited neurometabolic disease patients European Journal of Pediatrics ·Viviana Giannuzzi,Hugo Devlieger,Lucia Margari,Viveca Odlind,Lamis Ragab,Cinzia Maria Bellettato,Francesca D’Avanzo,Christina Lampe,Linda Cassis,Elisenda Cortès‐Saladelafont,Àngels García Cazorla,Ivo Barić,Ljerka Cvitanović-Šojat,Ksenija Fumić,Christine í Dali,Franco Bartoloni,Fedele Bonifazi,Maurizio Scarpa,Adriana Ceci	2017	10
8	Familial cerebral abscesses caused by hereditary hemorrhagic telangiectasia Clinical Case Reports ·Pernille Mathiesen Tørring,Mathilde Faurholdt Lauridsen,Christine í Dali,Poul Erik Andersen,Lilian Bomme Ousager,Klaus Brusgaard,Anette Drøhse Kjeldsen	2017	1
9	Intrathecal delivery of recombinant human arylsulfatase A in children with late-infantile metachromatic leukodystrophy: an update following extended treatment Molecular Genetics and Metabolism ·Caroline Sevin,Christine í Dali,Roberto Giugliani,Joachim Riethmüller,Christopher Troedson,Norio Sakai,Parul Bhargava,Douglas A. Kerr,Margaret Wasilewski	2017	4
10	A Novel TTBK2 De Novo Mutation in a Danish Family with Early-Onset Spinocerebellar Ataxia The Cerebellum ·Suzanne Granhøj Lindquist,Lisbeth Birk Møller,Christine í Dali,Lisbeth Marner,Erik‐Jan Kamsteeg,Jørgen E. Nielsen,Lena E. Hjermind	2016	11
11	Metachromatic Leukodystrophy Journal of Child Neurology ·Florian Eichler,Timothy M. Cox,Eric Crombez,Christine í Dali,Alfried Kohlschütter	2016	26
12	Intrathecal delivery of recombinant human arylsulfatase A in children with late-infantile metachromatic leukodystrophy Molecular Genetics and Metabolism ·Christine í Dali,Caroline Sevin,Joachim Riethmüller,Roberto Giugliani,Christopher Troedson,Parul Bhargava,Anna Wijatyk	2016	2
13	Alpha-mannosidosis: correlation between phenotype, genotype and mutant MAN2B1 subcellular localisation Orphanet Journal of Rare Diseases ·Line Borgwardt,Hilde Monica Frostad Riise Stensland,Klaus J Olsen,Flemming Wibrand,Helle Bagterp Klenow,Michael Beck,Yasmina Amraoui,Laila Arash,J. Fogh,Øivind Nilssen,Christine í Dali,Allan M. Lund	2015	32
14	Alpha‐mannosidosis: characterization of CNS pathology and correlation between CNS pathology and cognitive function Clinical Genetics ·Lise Borgwardt,Else Rubæk Danielsen,C. Thomsen,Jan‐Eric Månsson,N. Taouatas,A. M. Thuesen,K. J. Olsen,J. Fogh,Christine í Dali,Allan M. Lund	2015	11
15	Cowden Syndrome and Concomitant Pulmonary Neuroendocrine Tumor: A Presentation of Two Cases Case Reports in Medicine ·Seppo W. Langer,Lene Ringholm,Christine í Dali,René Horsleben Petersen,Åse Krogh Rasmussen,Anne‐Marie Gerdes,Birgitte Federspiel,Ulrich Knigge	2015	7
16	Sulfatide levels correlate with severity of neuropathy in metachromatic leukodystrophy Annals of Clinical and Translational Neurology ·Christine í Dali,Norman W. Barton,Mohamed H. Farah,Mihai Moldovan,Jan‐Eric Månsson,Nitin Nair,Morten Dunø,Lotte Risom,Hongmei Cao,Luying Pan,M. Sellos-Moura,Andrea M. Corse,Christian Krarup	2015	33
17	Alternating hemiplegia of childhood in Denmark: Clinical manifestations and ATP1A3 mutation status European Journal of Paediatric Neurology ·Christina Engel Hoei‐Hansen,Christine í Dali,Troels Lyngbye,Morten Dunø,Peter Uldall	2013	27
18	Enzyme Replacement Therapy for Patients with Alpha-Mannosidosis Molecular Genetics and Metabolism ·Line Borgwardt,Christine í Dali,J. Fogh,K. J. Olsen,Jan-Eric Maansson,Hans Christian Beck,Allan M. Lund	2012	2
19	Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course Journal of Inherited Metabolic Disease ·Samuel Groeschel,Christiane Kehrer,Corinna Engel,Christine í Dali,Annette Bley,Robert Steinfeld,Wolfgang Grodd,Ingeborg Krägeloh‐Mann	2011	57
20	Threshold electrical stimulation (TES) in ambulant children with CP: a randomized double-blind placebo-controlled clinical trial Developmental Medicine & Child Neurology ·Christine í Dali,Flemming Juul Hansen,Søren Anker Pedersen,Liselotte Skov,Jørgen Hilden,Inge Bjørnskov,Charlotte Strandberg,Jette Christensen,Ulla Haugsted,Grethe Herbst,Ulla Lyskjær	2002	32

About Christine í Dali

Christine í Dali is a scholar working on Physiology, Genetics and Hematology, having authored 28 papers that have together received 532 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (21 papers), RNA regulation and disease (4 papers), Trypanosoma species research and implications (4 papers), Autoimmune and Inflammatory Disorders Research (3 papers), Cerebral Palsy and Movement Disorders (3 papers), Neonatal and fetal brain pathology (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Neuroinflammation and Neurodegeneration Mechanisms (2 papers). The work is most often cited by research in Physiology (323 citations), Physiology (39 citations) and Neurology (43 citations). Christine í Dali has collaborated with scholars based in Denmark, Germany and United States. Frequent co-authors include Allan M. Lund, Ingeborg Krägeloh‐Mann, Line Borgwardt, Samuel Groeschel, J. Fogh, Morten Dunø, Christiane Kehrer, Margaret Wasilewski, Norman W. Barton and Nitin Nair. Their work appears in journals such as Neurology, Developmental Medicine & Child Neurology and Orphanet Journal of Rare Diseases.

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.

Explore authors with similar magnitude of impact