Julie Vogt

4.9k total citations
25 papers, 476 citations indexed

About

Julie Vogt is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Julie Vogt has authored 25 papers receiving a total of 476 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 9 papers in Genetics. Recurrent topics in Julie Vogt's work include Neurogenetic and Muscular Disorders Research (7 papers), Congenital heart defects research (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Julie Vogt is often cited by papers focused on Neurogenetic and Muscular Disorders Research (7 papers), Congenital heart defects research (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Julie Vogt collaborates with scholars based in United Kingdom, United States and Netherlands. Julie Vogt's 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 and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Journal of Clinical Microbiology.

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 of co-authors of Julie Vogt

This figure shows the co-authorship network connecting the top 25 collaborators of Julie Vogt. A scholar is included among the top collaborators of Julie Vogt 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 Julie Vogt. Julie Vogt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Trajectories from single-cells to PAX5-driven leukemia reveal PAX5-MYC interplay in vivo 2025 ·Leukemia ·Franziska Auer, (unknown), (unknown), (unknown), (unknown), Julie Vogt, (unknown), (unknown), (unknown), Andrea Hänel, Anna Viitasalo, Ulrike Friedrich, Andreas Dahl, (unknown), Aleksandra A. Pandyra, Polina Stepensky, Masatoshi Takagi, Arndt Borkhardt, (unknown), Julia Hauer	1
2	Impact of rapid genomic testing on clinical outcomes of acutely unwell children presenting with severe epilepsy 2025 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Lucy Hanington, Andrew Parrish, (unknown), (unknown), John Taylor, (unknown), (unknown), (unknown), Julie Vogt, Shilpa Naik, Mário Sá, Usha Kini	0
3	FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6 2024 ·Brain Communications ·Laura Watts, David J. Bunyan, Edoardo Giacopuzzi, Susan Walker, (unknown), N. Simon Thomas, Volker Straub, (unknown), (unknown), Julie Vogt, Shagufta Khan, Tracey Willis, Jenny C. Taylor, Alistair T. Pagnamenta	0
4	Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene 2024 ·Neuromuscular Disorders ·Kay E. Davies, Julie Vogt	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 2022 ·American Journal of Medical Genetics Part A ·(unknown), Tracey Willis, Nigel Kiely, Gunnar Houge, Julie Vogt	2
6	Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease 2021 ·Human Molecular Genetics ·(unknown), (unknown), Kyle Thompson, Emanuele Bellacchio, Courtney E. French, (unknown), Toni S. Pearson, Julie Vogt, Daria Diodato, (unknown), Anja Ernst, Rita Horváth, Manali Chitre, Jakob Ek, Flemming Wibrand, Dorothy K. Grange, Lucy Raymond, Xiao-Long Zhou, Robert W. Taylor, Elsebet Østergaard	13
7	Second‐trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray 2020 ·SHILAP Revista de lepidopterología ·(unknown), Mark D. Kilby, Julie Vogt, Fiona S. Togneri, E Quinlan-Jones, (unknown), Stephanie Allen, Dominic McMullan	8
8	Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype 2019 ·Clinical Genetics ·(unknown), (unknown), (unknown), 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)	21
9	Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect 2017 ·The Journal of Clinical Endocrinology & Metabolism ·Emma Webb, Meena Balasubramanian, Nadja Fratzl‐Zelman, Wayne A. Cabral, Hannah Titheradge, (unknown), Vrinda Saraff, Julie Vogt, Trevor Cole, Susan E. Stewart, Nicola Crabtree, (unknown), Sonja Gamsjaeger, Eleftherios P. Paschalis, Paul Roschger, Klaus Klaushofer, Nick J. Shaw, Joan C. Marini, Wolfgang Högler	28
10	MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus 2017 ·PLoS Genetics ·Patricia Blanchet, Martina Bebin, (unknown), Gregory M. Cooper, Michelle L. Thompson, Bénédicte Duban‐Bedu, Bénédicte Gérard, Amélie Piton, (unknown), Charu Deshpande, Virginia Clowes, Julie Vogt, Peter D. Turnpenny, Michael P. Williamson, Yves Alembik, Eric Glasgow, Alisdair McNeill	49
11	Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report 2016 ·BMC Research Notes ·(unknown), Isabel Colmenero, Nicola Ragge, Emma L. Blakely, Langping He, Robert McFarland, Robert W. Taylor, Julie Vogt, David V. Milford	16
12	A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies 2015 ·American Journal of Medical Genetics Part A ·Jonathan D. J. Labonne, Julie Vogt, (unknown), (unknown), Lawrence C. Layman, Hyung‐Goo Kim	25
13	Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome 2014 ·Acta Neuropathologica Communications ·Arthur B. McKie, (unknown), Julie Vogt, Kyra E. Stuurman, Marjan M. Weiss, (unknown), 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	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 2014 ·Human Mutation ·Denny Schanze, (unknown), Valérie Cormier‐Daire, Marie-Ange Delrue, Anne Dieux‐Coëslier, Tomonobu Hasegawa, Eva Holmberg, Rainer Koenig, (unknown), Ina Schanze, E Seemanová, Adam Shaw, Julie Vogt, Marianne Volleth, André Reis, Peter Meinecke, Raoul C. M. Hennekam, Martin Zenker	23
15	CHRNG genotype–phenotype correlations in the multiple pterygium syndromes 2011 ·Journal of Medical Genetics ·Julie Vogt, Neil V. Morgan, (unknown), 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	30
16	Germline mutation in DOK7 associated with fetal akinesia deformation sequence 2009 ·Journal of Medical Genetics ·Julie Vogt, Neil V. Morgan, Tamás Marton, Susan Maxwell, Benjamin J. Harrison, David Beeson, Eamonn R. Maher	45
17	Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients 2008 ·The American Journal of Human Genetics ·Julie Vogt, Benjamin J. Harrison, Hayley Spearman, Judy Cossins, Sascha Vermeer, (unknown), Neil V. Morgan, David Beeson, Eamonn R. Maher	75
18	The tale of a nail sign in chromosome 4q34 deletion syndrome 2006 ·Clinical Dysmorphology ·Julie Vogt, (unknown), Marc Tischkowitz, William Reardon, Louise Brueton	26
19	Unique Case of Helicobacter sp. Osteomyelitis in an Immunocompetent Child Diagnosed by Broad-Range 16S PCR 2002 ·Journal of Clinical Microbiology ·Kathryn Harris, Katy Fidler, John C. Hartley, Julie Vogt, Nigel Klein, Fergal Monsell, Vas Novelli	31
20	Staining of sensory and motor nerves in muscles with sudan black B 1964 ·The Journal of Pathology and Bacteriology ·John Cavanagh, (unknown), Julie Vogt	16

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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