Daniela T. Pilz

11.0k total citations
72 papers, 3.6k citations indexed

About

Daniela T. Pilz is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Daniela T. Pilz has authored 72 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 36 papers in Genetics and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Daniela T. Pilz's work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Fetal and Pediatric Neurological Disorders (13 papers). Daniela T. Pilz is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Fetal and Pediatric Neurological Disorders (13 papers). Daniela T. Pilz collaborates with scholars based in United Kingdom, United States and Italy. Daniela T. Pilz's co-authors include William B. Dobyns, David H. Ledbetter, Thomas D. Cushion, Neil Stoodley, Andrew E. Fry, Naomichi Matsumoto, Richard J. Leventer, Mark I. Rees, Oliver Quarrell and Richard C. Trembath and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

Daniela T. Pilz

70 papers receiving 3.5k citations

Peers

Daniela T. Pilz

GENET

PPCH

CMN

Alexander G. Bassuk United States

Yuanyi Feng United States

Laurence Colleaux France

Rolph Pfundt Netherlands

Susan Lindsay United Kingdom

Wenli Gu China

Helen J. Eyre Australia

Marlène Rio France

Paweł Stankiewicz United States

Monica J. Justice United States

Alexander G. Bassuk United States

Daniela T. Pilz

2.4k ×1.3

1.0k ×0.6

GENET

408 ×0.5

PPCH

569 ×0.8

390 ×0.9

CMN

Citations per year, relative to Daniela T. Pilz Daniela T. Pilz (= 1×) peers Alexander G. Bassuk

Countries citing papers authored by Daniela T. Pilz

Since Specialization

Citations

This map shows the geographic impact of Daniela T. Pilz'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 Daniela T. Pilz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela T. Pilz more than expected).

Fields of papers citing papers by Daniela T. Pilz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniela T. Pilz. 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 Daniela T. Pilz. The network helps show where Daniela T. Pilz may publish in the future.

Co-authorship network of co-authors of Daniela T. Pilz

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela T. Pilz. A scholar is included among the top collaborators of Daniela T. Pilz 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 Daniela T. Pilz. Daniela T. Pilz 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

Yao, Baojin, Tommaso Pippucci, Joshua D. Smith, et al.. (2019). De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism. The American Journal of Human Genetics. 104(4). 777–777. 6 indexed citations

Agnol, Alais Maria Dall, Daniela T. Pilz, Raquel Arruda Leme, et al.. (2019). Detection of Equid gammaherpesvirus 2 and 5 DNA in the upper respiratory tract of asymptomatic horses from Southern Brazil. Brazilian Journal of Microbiology. 50(3). 875–878. 5 indexed citations

O’Neill, Adam C., Christina Kyrousi, Richard J. Leventer, et al.. (2018). A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration. Cell Reports. 25(10). 2729–2741.e6. 34 indexed citations

Kogelenberg, Margriet van, Alice R. Clark, Zandra A. Jenkins, et al.. (2015). Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA. Journal of Molecular Medicine. 93(7). 773–782. 9 indexed citations

Fry, Andrew E., Thomas D. Cushion, & Daniela T. Pilz. (2014). The genetics of lissencephaly. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(2). 198–210. 67 indexed citations

Cushion, Thomas D., William B. Dobyns, Jonathan G.L. Mullins, et al.. (2013). Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain. 136(2). 536–548. 101 indexed citations

Østergaard, Pia, Michael A. Simpson, Fiona Connell, et al.. (2011). Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nature Genetics. 43(10). 929–931. 348 indexed citations

O’Driscoll, Mary, Sarah B. Daly, Jill Urquhart, et al.. (2010). Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria. The American Journal of Human Genetics. 87(3). 354–364. 92 indexed citations

Abdollahi, Mohammad Reza, Ewan E. Morrison, Tamara Sirey, et al.. (2009). Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia. The American Journal of Human Genetics. 85(5). 737–744. 122 indexed citations

10.

Fry, Andrew E., Claus Klingenberg, Jean Matthes, et al.. (2009). Connective tissue involvement in two patients with features of cranioectodermal dysplasia. American Journal of Medical Genetics Part A. 149A(10). 2212–2215. 11 indexed citations

11.

Mei, Davide, Ruth Lewis, Elena Parrini, et al.. (2008). High frequency of genomic deletions—and a duplication—in the LIS1 gene in lissencephaly: implications for molecular diagnosis. Journal of Medical Genetics. 45(6). 355–361. 30 indexed citations

12.

Aligianis, Irene A., Neil V. Morgan, Marina Mione, et al.. (2006). Mutation in Rab3 GTPase-Activating Protein (RAB3GAP) Noncatalytic Subunit in a Kindred with Martsolf Syndrome. The American Journal of Human Genetics. 78(4). 702–707. 78 indexed citations

13.

Evans, Julie, Hayley Archer, James Colley, et al.. (2005). Early onset seizures and Rett-like features associated with mutations in CDKL5. European Journal of Human Genetics. 13(10). 1113–1120. 135 indexed citations

14.

Chandler, Kate, Karl Rakshi, Kelly Springell, et al.. (2005). Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16. Brain. 129(1). 272–277. 6 indexed citations

15.

Cardoso, Tereza Cristina & Daniela T. Pilz. (2004). Wild rabies virus detection by plaque assay from naturally infected brains in different species. Veterinary Microbiology. 103(3-4). 161–167. 8 indexed citations

16.

Matsumoto, Naomichi, Richard J. Leventer, Stephanie K. Mewborn, et al.. (2001). Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia. European Journal of Human Genetics. 9(1). 5–12. 114 indexed citations

17.

Leventer, Richard J., Daniela T. Pilz, Naomichi Matsumoto, David H. Ledbetter, & William B. Dobyns. (2000). Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis. Molecular Medicine Today. 6(7). 277–284. 16 indexed citations

18.

Pilz, Daniela T., J. Kuć, Naomichi Matsumoto, et al.. (1999). Subcortical Band Heterotopia in Rare Affected Males Can be Caused by Missense Mutations in DCX (XLIS) or LIS1. Human Molecular Genetics. 8(9). 1757–1760. 107 indexed citations

19.

Tyfield, Linda, F. Cockburn, J. L. Bidwell, et al.. (1997). Sequence variation at the phenylalanine hydroxylase gene in the British Isles.. PubMed Central. 60(2). 388–96. 19 indexed citations

20.

Pilz, Daniela T. & Oliver Quarrell. (1996). Syndromes with lissencephaly.. Journal of Medical Genetics. 33(4). 319–323. 43 indexed citations

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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