Julie Vogt

4.9k citations

25 papers · 476 indexed · h-index 14

Genetics top 10%
- Neurogenetic and Muscular Disorders Research 7
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
Genetics top 10%
- Neurogenetic and Muscular Disorders Research 7
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
Molecular Biology
- Congenital heart defects research 5
- Mitochondrial Function and Pathology 2
Clinical Biochemistry
Parasitology
Pulmonary and Respiratory Medicine
- Neonatal Respiratory Health Research 4
Pathology and Forensic Medicine
- Spinal Cord Injury Research 3

Co-authors: Eamonn R. Maher Neil V. Morgan Benjamin J. Harrison David Beeson Judy Cossins Sascha Vermeer Hayley Spearman Louise Brueton
Cited by: Genetics Molecular Biology
Journals: SHILAP Revista de lepidopterología (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)Journal of Clinical Microbiology (1 paper)
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Julie Vogt

22 papers receiving 454 citations

Peers

Countries citing papers authored by Julie Vogt

Since Specialization

Citations

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

Fields of papers citing papers by Julie Vogt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Trajectories from single-cells to PAX5-driven leukemia reveal PAX5-MYC interplay in vivo Leukemia ·Franziska Auer,Mina N.F. Morcos,Mikko Sipola,Irfan Akhtar,Sanni Moisio,Julie Vogt,R Haag,Mari Lahnalampi,Tiina J Tuononen,Andrea Hänel,Anna Viitasalo,Ulrike Friedrich,Andreas Dahl,Carolin Prexler,Aleksandra A. Pandyra,Polina Stepensky,Masatoshi Takagi,Arndt Borkhardt,(unknown),Julia Hauer	2025	1
2	Impact of rapid genomic testing on clinical outcomes of acutely unwell children presenting with severe epilepsy European Journal of Human Genetics ·Erina Sasaki,Philip Millington,Taisiia Sazonova,Lucy Hanington,Andrew Parrish,Benito Baños-Piñero,Helen Lord,John Taylor,Ramanand Jeeneea,Charlotte Sherlaw‐Sturrock,Amitav Parida,Julie Vogt,Shilpa Naik,Mário Sá,Usha Kini	2025	0
3	FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6 Brain Communications ·Laura Watts,David J. Bunyan,Edoardo Giacopuzzi,Susan Walker,Gabriella Gazdagh,N. Simon Thomas,Volker Straub,Anne-Marie Childs,Joan Forsyth,Julie Vogt,Shagufta Khan,Tracey Willis,Jenny C. Taylor,Alistair T. Pagnamenta	2024	0
4	Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene Neuromuscular Disorders ·Kay E. Davies,Julie Vogt	2024	3
5	PIEZO2‐related distal arthrogryposis type 5: Longitudinal follow‐up of a three‐generation family broadens phenotypic spectrum, complications, and health surveillance recommendations for this patient group American Journal of Medical Genetics Part A ·Charlotte Sherlaw‐Sturrock,Tracey Willis,Nigel Kiely,Gunnar Houge,Julie Vogt	2022	2
6	Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease Human Molecular Genetics ·Wen-Qiang Zheng,Signe Vandal Pedersen,Kyle Thompson,Emanuele Bellacchio,Courtney E. French,Benjamin Munro,Toni S. Pearson,Julie Vogt,Daria Diodato,Tue Diemer,Anja Ernst,Rita Horváth,Manali Chitre,Jakob Ek,Flemming Wibrand,Dorothy K. Grange,Lucy Raymond,Xiao-Long Zhou,Robert W. Taylor,Elsebet Østergaard	2021	13
7	Second‐trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray SHILAP Revista de lepidopterología ·Małgorzata Drożniewska,Mark D. Kilby,Julie Vogt,Fiona S. Togneri,E Quinlan-Jones,Lisa Reali,Stephanie Allen,Dominic McMullan	2020	8
8	Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype Clinical Genetics ·Jessica A. Radley,Rory O’Sullivan,Sarah Turton,Helen Cox,Julie Vogt,Jenny Morton,Elizabeth A. Jones,Sarah Smithson,Katherine Lachlan,Julia Rankin,Jill Clayton‐Smith,Josh Willoughby,Frances Elmslie,Francis H. Sansbury,Nicola Cooper,(unknown),(unknown)	2019	21
9	Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect The Journal of Clinical Endocrinology & Metabolism ·Emma Webb,Meena Balasubramanian,Nadja Fratzl‐Zelman,Wayne A. Cabral,Hannah Titheradge,Atif Alsaedi,Vrinda Saraff,Julie Vogt,Trevor Cole,Susan E. Stewart,Nicola Crabtree,Brandi M. Sargent,Sonja Gamsjaeger,Eleftherios P. Paschalis,Paul Roschger,Klaus Klaushofer,Nick J. Shaw,Joan C. Marini,Wolfgang Högler	2017	28
10	MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus PLoS Genetics ·Patricia Blanchet,Martina Bebin,Shaam Bruet,Gregory M. Cooper,Michelle L. Thompson,Bénédicte Duban‐Bedu,Bénédicte Gérard,Amélie Piton,Sylvie Suckno,Charu Deshpande,Virginia Clowes,Julie Vogt,Peter D. Turnpenny,Michael P. Williamson,Yves Alembik,Eric Glasgow,Alisdair McNeill	2017	49
11	Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report BMC Research Notes ·Asheeta Gupta,Isabel Colmenero,Nicola Ragge,Emma L. Blakely,Langping He,Robert McFarland,Robert W. Taylor,Julie Vogt,David V. Milford	2016	16
12	A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies American Journal of Medical Genetics Part A ·Jonathan D. J. Labonne,Julie Vogt,Lisa Reali,Il‐Keun Kong,Lawrence C. Layman,Hyung‐Goo Kim	2015	25
13	Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome Acta Neuropathologica Communications ·Arthur B. McKie,Atif Alsaedi,Julie Vogt,Kyra E. Stuurman,Marjan M. Weiss,Hassan Shakeel,Louise Tee,Neil V. Morgan,Peter G. J. Nikkels,Gijs van Haaften,Soo‐Mi Park,Jasper J. van der Smagt,Marianna Bugiani,Eamonn R. Maher	2014	18
14	Deletions in the 3′ Part of theNFIXGene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall-Smith Syndrome Human Mutation ·Denny Schanze,D. Neubauer,Valérie Cormier‐Daire,Marie-Ange Delrue,Anne Dieux‐Coëslier,Tomonobu Hasegawa,Eva Holmberg,Rainer Koenig,Gabriele Krueger,Ina Schanze,E Seemanová,Adam Shaw,Julie Vogt,Marianne Volleth,André Reis,Peter Meinecke,Raoul C. M. Hennekam,Martin Zenker	2014	23
15	CHRNG genotype–phenotype correlations in the multiple pterygium syndromes Journal of Medical Genetics ·Julie Vogt,Neil V. Morgan,Pauline Rehal,Laurence Bonhomme‐Faivre,Louise Brueton,Kristin Becker,Jean‐Pierre Fryns,Sue Holder,Lily Islam,Emma Kivuva,Sally Ann Lynch,Renaud Touraine,Louise C. Wilson,Fiona MacDonald,Eamonn R. Maher	2011	30
16	Germline mutation in DOK7 associated with fetal akinesia deformation sequence Journal of Medical Genetics ·Julie Vogt,Neil V. Morgan,Tamás Marton,Susan Maxwell,Benjamin J. Harrison,David Beeson,Eamonn R. Maher	2009	45
17	Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients The American Journal of Human Genetics ·Julie Vogt,Benjamin J. Harrison,Hayley Spearman,Judy Cossins,Sascha Vermeer,Lambert Naudin ten Cate,Neil V. Morgan,David Beeson,Eamonn R. Maher	2008	75
18	The tale of a nail sign in chromosome 4q34 deletion syndrome Clinical Dysmorphology ·Julie Vogt,E. Ryan,Marc Tischkowitz,William Reardon,Louise Brueton	2006	26
19	Unique Case of Helicobacter sp. Osteomyelitis in an Immunocompetent Child Diagnosed by Broad-Range 16S PCR Journal of Clinical Microbiology ·Kathryn Harris,Katy Fidler,John C. Hartley,Julie Vogt,Nigel Klein,Fergal Monsell,Vas Novelli	2002	31
20	Staining of sensory and motor nerves in muscles with sudan black B The Journal of Pathology and Bacteriology ·John Cavanagh,R. J. Passingham,Julie Vogt	1964	16

About Julie Vogt

Julie Vogt is a scholar working on Genetics, Genetics and Parasitology, having authored 25 papers that have together received 476 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (7 papers), Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers), Neonatal Respiratory Health Research (4 papers), Spinal Cord Injury Research (3 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Genetics (117 citations), Genetics (200 citations) and Molecular Biology (234 citations). Julie Vogt has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Eamonn R. Maher, Neil V. Morgan, Benjamin J. Harrison, David Beeson, Judy Cossins, Sascha Vermeer, Hayley Spearman, Louise Brueton, Susan Maxwell and Tamás Marton. Their work appears in journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Journal of Clinical Microbiology.

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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