Rolf W. Stottmann

2.7k total citations
63 papers, 1.8k citations indexed

About

Rolf W. Stottmann is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Rolf W. Stottmann has authored 63 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 36 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Rolf W. Stottmann's work include Hedgehog Signaling Pathway Studies (14 papers), Genetic and Kidney Cyst Diseases (13 papers) and Epigenetics and DNA Methylation (11 papers). Rolf W. Stottmann is often cited by papers focused on Hedgehog Signaling Pathway Studies (14 papers), Genetic and Kidney Cyst Diseases (13 papers) and Epigenetics and DNA Methylation (11 papers). Rolf W. Stottmann collaborates with scholars based in United States, Egypt and Germany. Rolf W. Stottmann's co-authors include John Klingensmith, David R. Beier, Ryan M. Anderson, Murim Choi, Pamela V. Tran, Annick Turbé-Doan, Erik N. Meyers, Daniel Bachiller, Yuji Mishina and Tatiana Y. Besschetnova and has published in prestigious journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Rolf W. Stottmann

59 papers receiving 1.8k citations

Peers

Countries citing papers authored by Rolf W. Stottmann

Since Specialization

Citations

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

Fields of papers citing papers by Rolf W. Stottmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rolf W. Stottmann. 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 Rolf W. Stottmann. The network helps show where Rolf W. Stottmann may publish in the future.

Co-authorship network of co-authors of Rolf W. Stottmann

This figure shows the co-authorship network connecting the top 25 collaborators of Rolf W. Stottmann. A scholar is included among the top collaborators of Rolf W. Stottmann 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 Rolf W. Stottmann. Rolf W. Stottmann 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	Mouse variants in Taf1c result in reduced survival to birth 2025 ·Developmental Biology ·Jennifer L. Watts, (unknown), Rolf W. Stottmann	0
2	Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis 2025 ·Development ·(unknown), (unknown), (unknown), Yoann Saillour, (unknown), (unknown), (unknown), Rolf W. Stottmann, Nadia Bahi‐Buisson, Alessandra Pierani, Nathalie Spassky, Frédéric Causeret	0
3	Long‐read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalities 2024 ·American Journal of Medical Genetics Part A ·Kristen L. Sund, (unknown), Joyce Lee, John Garbe, Zakia Abdelhamed, (unknown), Barbara Hallinan, (unknown), (unknown), (unknown), Rolf W. Stottmann, Teresa A. Smolarek, Lisa Dyer, Matthew S. Hestand	3
4	Expanding the phenotypic spectrum of CSNK2A1-associated Okur-Chung neurodevelopmental syndrome 2024 ·Human Genetics and Genomics Advances ·Swetha Ramadesikan, (unknown), (unknown), Allison C. Daley, Liz Varga, Gurusamy Umamaheswaran, Matthew Pastore, Emily Sites, (unknown), Dennis W. Bartholomew, Jesse M. Hunter, Peter D. White, Richard K. Wilson, Rolf W. Stottmann, Daniel C. Koboldt	1
5	A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development 2024 ·Nature Communications ·Andrea Wilderman, (unknown), Machteld Baetens, (unknown), (unknown), (unknown), Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E. Miller, (unknown), Kari M. Brown, Rolf W. Stottmann, Sarah Vergult, K. Nicole Weaver, Samantha A. Brugmann, Timothy C. Cox, Justin Cotney	3
6	Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations 2023 ·Development ·(unknown), Megan N. Michalski, (unknown), (unknown), (unknown), (unknown), Cassandra R. Diegel, Zhendong Zhong, Bart O. Williams, Rolf W. Stottmann	2
7	PPP2R1A neurodevelopmental disorder is associated with congenital heart defects 2022 ·American Journal of Medical Genetics Part A ·Elizabeth Baker, (unknown), Ben Pode‐Shakked, Laura Cross, Bonnie Sullivan, Annick Raas‐Rothschild, (unknown), Ortal Barel, Omer Bar‐Yosef, Ammar Husami, Robert J. Hopkin, Carlos E. Prada, Rolf W. Stottmann, K. Nicole Weaver	7
8	Robin sequence without cleft palate: Genetic diagnoses and management implications 2021 ·American Journal of Medical Genetics Part A ·K. Nicole Weaver, Bonnie Sullivan, (unknown), (unknown), Barbara A. Chini, Brian S. Pan, Rolf W. Stottmann, Patricia L. Bender, Robert J. Hopkin, Xue Zhang, Howard M. Saal	6
9	A Novel Mutation in Cse1l Disrupts Brain and Eye Development with Specific Effects on Pax6 Expression 2021 ·Journal of Developmental Biology ·(unknown), (unknown), (unknown), Ronald R. Waclaw, Salil A. Lachke, Rolf W. Stottmann	0
10	A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay 2021 ·SHILAP Revista de lepidopterología ·(unknown), Alison M. Muir, (unknown), (unknown), Kristin G. Monaghan, (unknown), Ingrid M. Wentzensen, (unknown), Francesco Brancati, David J. Harris, (unknown), Rolf W. Stottmann, Carlos E. Prada, (unknown), Heather C. Mefford	4
11	Genetic and phenotypic heterogeneity in KIAA0753‐related ciliopathies 2021 ·American Journal of Medical Genetics Part A ·(unknown), Yuri A. Zárate, (unknown), Jürgen W. Spranger, Dan Doherty, Rolf W. Stottmann, K. Nicole Weaver	5
12	CNS glycosylphosphatidylinositol deficiency results in delayed white matter development, ataxia and premature death in a novel mouse model 2020 ·Human Molecular Genetics ·(unknown), (unknown), Rolf W. Stottmann	12
13	A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice 2020 ·Disease Models & Mechanisms ·Zakia Abdelhamed, (unknown), Sandra Cindrić, Heymut Omran, Rolf W. Stottmann	11
14	Mandibulofacial dysostosis with microcephaly: An expansion of the phenotype via parental survey 2020 ·American Journal of Medical Genetics Part A ·(unknown), Robert J. Hopkin, Patricia L. Bender, (unknown), (unknown), Bonnie Sullivan, Rolf W. Stottmann, Howard M. Saal, K. Nicole Weaver	7
15	Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants 2019 ·PLoS Genetics ·(unknown), William E. Gibbons, (unknown), Zakia Abdelhamed, Daniel R. Prows, Rolf W. Stottmann	5
16	Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development 2017 ·PLoS ONE ·(unknown), Elizabeth N. Schock, (unknown), Ching‐Fang Chang, (unknown), Pamela V. Tran, Samantha A. Brugmann, Rolf W. Stottmann	22
17	A tissue-specific role for intraflagellar transport genes during craniofacial development 2017 ·PLoS ONE ·Elizabeth N. Schock, Jaime Struve, Ching‐Fang Chang, Trevor Williams, (unknown), (unknown), Rolf W. Stottmann, Samantha A. Brugmann	25
18	Toward a systems‐level understanding of the Hedgehog signaling pathway: defining the complex, robust, and fragile 2012 ·WIREs Systems Biology and Medicine ·Pamela V. Tran, Salil A. Lachke, Rolf W. Stottmann	9
19	Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sites 2010 ·Genomics ·Savina Jaeger, Esther T. Chan, Michael F. Berger, Rolf W. Stottmann, Timothy R. Hughes, Martha L. Bulyk	38
20	BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium 2004 ·Development ·Rolf W. Stottmann, Murim Choi, Yuji Mishina, Erik N. Meyers, John Klingensmith	138

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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