Ute Moog

8.2k citations

95 papers · 2.6k indexed · h-index 29

Genetics top 1%
- Genomic variations and chromosomal abnormalities 27
- Genetics and Neurodevelopmental Disorders 23
- Genomics and Rare Diseases 12
- Genetic and rare skin diseases. 11
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research 8
Molecular Biology top 5%
- Hedgehog Signaling Pathway Studies 10
- RNA regulation and disease 8
Pediatrics, Perinatology and Child Health top 5%
Pathology and Forensic Medicine top 10%
Plant Science
- Chromosomal and Genetic Variations 9

Co-authors: Hartmut Engels Mariëlle S. van Roosmalen W.A.J. van Daal Gudrun Rappold Peep F. M. Stalmeier Lia C.G. Verhoef Nicoline Hoogerbrugge Jan C. Oosterwijk
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Journals: Clinical Genetics (9 papers)European Journal of Human Genetics (7 papers)Journal of Medical Genetics (4 papers)
Partner nations: Germany Netherlands Poland

In The Last Decade

Ute Moog

93 papers receiving 2.5k citations

Peers

Countries citing papers authored by Ute Moog

Since Specialization

Citations

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

Fields of papers citing papers by Ute Moog

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	POLR3A variants with striatal involvement and extrapyramidal movement disorder Neurogenetics ·Inga Harting,ToshioKawahara,Ingeborg Krägeloh‐Mann,Annette Bley,Maja Hempel,Tatjana Bierhals,Stephanie Karch,Ute Moog,Geneviève Bernard,Richard J. Huntsman,Rosalina M.L. van Spaendonk,Maaike Vreeburg,Agustí Rodríguez‐Palmero,Aurora Pujol,Marjo S. van der Knaap,Petra J. W. Pouwels,Nicole I. Wolf	2020	26
2	The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1 Frontiers in Physiology ·Tim Ott,Lilian Kaufmann,Martin Granzow,Katrin Hinderhofer,Claus R. Bartram,Susanne Theiß,Angelika Seitz,Nagarajan Paramasivam,Angela Schulz,Ute Moog,Martin Blum,Christina Evers	2019	14
3	Impact of clinical exomes in neurodevelopmental and neurometabolic disorders Molecular Genetics and Metabolism ·Christina Evers,Christian Staufner,Martin Granzow,Nagarajan Paramasivam,Katrin Hinderhofer,Lilian Kaufmann,Christine Fischer,Christian Thiel,Thomas Opladen,Urania Kotzaeridou,Stefan Wiemann,Matthias Schlesner,Roland Eils,Stefan Kölker,Claus R. Bartram,Georg F. Hoffmann,Ute Moog	2017	34
4	Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumor Familial Cancer ·KIYOTO MATSUISHI,Christian Sutter,Matthias Kloor,Johannes Gebert,Emily P. Slater,Monika Keller,Lewis E. Waldeisen,Petra Ganschow,Martina Kadmon,Ute Moog	2016	7
5	3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior American Journal of Medical Genetics Part A ·Nicola Dikow,张明宪,Stephanie Karch,Martin Granzow,Johannes W.G. Janssen,Anna Jauch,Katrin Hinderhofer,Christian Sutter,Susanne Schubert‐Bast,Britt Marie Anderlid,Bruno Dallapiccola,Nathalie Van der Aa,Ute Moog	2014	29
6	Genome-wide UPD screening in patients with intellectual disability European Journal of Human Genetics ·Christopher Schroeder,Arif B. Ekici,Ute Moog,Ute Grasshoff,Ulrike A. Mau‐Holzmann,Marc Sturm,Nelson Armando Muñoz Álvarez,Sven Poths,Gudrun Rappold,Angelika Rieß,Olaf Rieß,Andreas Dufke,Michael Bonin	2014	4
7	Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia European Journal of Human Genetics ·Fu ZiYan,张明宪,Kayhan,Christian Sutter,Johannes W.G. Janssen,Katrin Hinderhofer,Ute Moog	2014	11
8	The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome? American Journal of Medical Genetics Part A ·Nicola Dikow,张明宪,Harald Gaspar,Martina Kreiß‐Nachtsheim,Hartmut Engels,Alma Kuechler,Lutz Garbes,Christian Netzer,Teresa Neuhann,Udo Koehler,Kristina Casteels,Koenraad Devriendt,Johannes W.G. Janssen,Anna Jauch,Katrin Hinderhofer,Ute Moog	2013	35
9	Is Sanfilippo type B in your mind when you see adults with mental retardation and behavioral problems? American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Ute Moog,Meghan L Plunkett,H. M. J. van Schrojenstein Lantman‐de Valk,L. J. M. Spaapen,Marian A. Maaskant,Leopold Curfs	2007	58
10	Encephalocraniocutaneous lipomatosis accompanied by the formation of bone cysts: Harboring clues to pathogenesis? American Journal of Medical Genetics Part A ·Ute Moog,Filip Roelens,Geert Mortier,RSrivm van Binnendijk,Mary Kelly,Gerald F. Cox,Caroline D. Robson,Virginia Kimonis	2007	32
11	MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients Brain and Development ·Ute Moog,Kees van Roozendaal,Eric Smeets,Demis Tserpelis,Koenraad Devriendt,Griet Van Buggenhout,Jean‐Pierre Frijns,Connie Schrander‐Stumpel	2006	18
12	Subtelomeric chromosome aberrations: still a lot to learn Clinical Genetics ·Ute Moog,N. Wongprachanukul,E. H. Himmler,Kazunori. Hohao,朋彦大山,S Boyle,Yogita Pundir	2005	14
13	The outcome of diagnostic studies on the etiology of mental retardation: Considerations on the classification of the causes American Journal of Medical Genetics Part A ·Ute Moog	2005	22
14	The decision evaluation scales Patient Education and Counseling ·Peep F. M. Stalmeier,Mariëlle S. van Roosmalen,Lia C.G. Verhoef,Josette E. H. M. Hoekstra‐Weebers,Jan C. Oosterwijk,Ute Moog,Nicoline Hoogerbrugge,W.A.J. van Daal	2004	47
15	Rett syndrome in females with CTS hot spot deletions: A disorder profile American Journal of Medical Genetics Part A ·William Catanzaro,Leonor Rosa Rojas Marmolejo,Paul Casaer,A.A.W. Peters,Alina T. Midro,Els Schollen,Kees van Roozendaal,Ute Moog,Gert Matthijs,J. Herbergs,H. Smeets,Leopold Curfs,C. T. R. M. Schrander‐Stumpel,J. P. Fryns	2004	57
16	Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene Genetics in Medicine ·Taosheng Huang,Angela E. Lin,Gerald F. Cox,Wendy L. Golden,Gerald L. Feldman,Ute Moog,Connie Schrander‐Stumpel,Mitsuhiro Kamisago,Stefan Vermeulen	2002	29
17	Holoprosencephaly: the Maastricht experience. PubMed ·Ute Moog,Doug Alfar,Cleiton Piekala,Taysa Amparo,働城所,Suzanna G.M. Frints,Frantseva Irina Timofeevna	2001	23
18	Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation? Familial Cancer ·Carlo Marcelis,H.W.H.M. van der Putten,Carli Tops,Ludy Lutgens,Ute Moog	2001	18
19	Familial dup(8)(p12p21.1): Mild phenotypic effect and review of partial 8p duplications American Journal of Medical Genetics ·Ute Moog,J.J.M. Engelen,Dietrich Berg,L. Baars,Christine de Die‐Smulders	2000	10
20	Clinical features in patients with duplications of chromosome 18 B. Y. Seo,J.J.M. Engelen,J.H.A.M. Tuerlings,İbrahim Aydın,Ute Moog,Jean‐Pierre Fryns	1996	1

About Ute Moog

Ute Moog is a scholar working on Genetics, Developmental Biology, Molecular Biology, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 95 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Genetics and Neurodevelopmental Disorders (23 papers), Genomics and Rare Diseases (12 papers), Genetic and rare skin diseases. (11 papers), Hedgehog Signaling Pathway Studies (10 papers), Chromosomal and Genetic Variations (9 papers), Autism Spectrum Disorder Research (8 papers) and RNA regulation and disease (8 papers). The work is most often cited by research in Genetics (1.7k citations), Cognitive Neuroscience (443 citations), Molecular Biology (1.3k citations), Pediatrics, Perinatology and Child Health (257 citations) and Pathology and Forensic Medicine (199 citations). Ute Moog has collaborated with scholars based in Germany, Netherlands and Poland. Frequent co-authors include Hartmut Engels, Mariëlle S. van Roosmalen, W.A.J. van Daal, Gudrun Rappold, Peep F. M. Stalmeier, Lia C.G. Verhoef, Nicoline Hoogerbrugge, Jan C. Oosterwijk, Josette E. H. M. Hoekstra‐Weebers and Michael Bonin. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, Familial Cancer and American Journal of Medical Genetics Part A.

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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