Stephan C. Collins

5.0k total citations · 1 hit paper
45 papers, 2.1k citations indexed

About

Stephan C. Collins is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Stephan C. Collins has authored 45 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 23 papers in Surgery and 18 papers in Genetics. Recurrent topics in Stephan C. Collins's work include Pancreatic function and diabetes (22 papers), Metabolism, Diabetes, and Cancer (9 papers) and Adipose Tissue and Metabolism (7 papers). Stephan C. Collins is often cited by papers focused on Pancreatic function and diabetes (22 papers), Metabolism, Diabetes, and Cancer (9 papers) and Adipose Tissue and Metabolism (7 papers). Stephan C. Collins collaborates with scholars based in United Kingdom, France and Switzerland. Stephan C. Collins's co-authors include Patrik Rorsman, Mirko Trajkovski, Mihaela Zavolan, Markus Stoffel, Jean Hausser, Matthias Braun, Matthew N. Poy, Dominique Gauguier, Anne Clark and Katherine E. Pinnick and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Stephan C. Collins

42 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

miR-375 maintains normal pancreatic α- and β-cell mass

2009 617 citations Matthew N. Poy, Jean Hausser et al. Proceedings of the National Academy of Sciences profile →

Peers

Countries citing papers authored by Stephan C. Collins

Since Specialization

Citations

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

Fields of papers citing papers by Stephan C. Collins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephan C. Collins. 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 Stephan C. Collins. The network helps show where Stephan C. Collins may publish in the future.

Co-authorship network of co-authors of Stephan C. Collins

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan C. Collins. A scholar is included among the top collaborators of Stephan C. Collins 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 Stephan C. Collins. Stephan C. Collins 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	CRISPR knockout screens reveal genes and pathways essential for neuronal differentiation and implicate PEDS1 in neurodevelopment 2026 ·Nature Neuroscience ·(unknown), Stephan C. Collins, (unknown), Nanako Hamada, (unknown), (unknown), (unknown), Tamar Harel, Koh-ichi Nagata, (unknown), (unknown)	0
2	De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes 2024 ·Life ·Yann Loe-Mie, (unknown), Caroline Dubertret, Takeo Yoshikawa, Binnaz Yalcin, Stephan C. Collins, Anne Boland, Jean‐François Deleuze, Philip Gorwood, (unknown), Michel Simonneau, Aude-Marie Lepagnol-Bestel	2
3	Automatic Segmentation of Histological Images of Mouse Brains 2023 ·Algorithms ·(unknown), Alain Lalande, Binnaz Yalcin, Fabrice Mériaudeau, Stephan C. Collins	0
4	Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development 2022 ·Nature Communications ·(unknown), Karine Poirier, Richard Belvindrah, Imane Moutkine, Anne Houllier, (unknown), Florence Petit, Anne Boland, Stephan C. Collins, Mariano Soiza‐Reilly, Binnaz Yalcin, Jamel Chelly, Jean‐François Deleuze, Nadia Bahi‐Buisson, Fiona Francis	4
5	A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice 2021 ·Molecular Biology and Evolution ·Michał Szpak, Stephan C. Collins, Yan Li, Xiao Liu, Qasim Ayub, (unknown), Valerie E. Vancollie, Christopher J. Lelliott, Yali Xue, Binnaz Yalcin, Huanming Yang, Chris Tyler‐Smith	0
6	Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth 2021 ·Human Genetics ·Médéric Jeanne, Marie‐Laure Vuillaume, (unknown), Valerie E. Vancollie, Christel Wagner, Stephan C. Collins, (unknown), Damien Haye, (unknown), Rolph Pfundt, (unknown), Marie‐Pierre Moizard, Sylviane Marouillat, Tjitske Kleefstra, Binnaz Yalcin, Frédéric Laumonnier, Annick Toutain	14
7	Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis 2019 ·Nature Communications ·Stephan C. Collins, (unknown), (unknown), Valerie E. Vancollie, Christel Wagner, (unknown), Helen Whitley, (unknown), (unknown), (unknown), Andrew Edwards, Hervé Moine, Jacqueline K. White, David J. Adams, Alexandre Reymond, Christopher J. Lelliott, Caleb Webber, Binnaz Yalcin	19
8	Glucose and hypothalamic astrocytes: More than a fueling role? 2015 ·Neuroscience ·Corinne Leloup, C. Allard, Lionel Carneiro, Xavier Fioramonti, Stephan C. Collins, Luc Pénicaud	47
9	Alteration of hypothalamic glucose and lactate sensing in 48 h hyperglycemic rats 2012 ·Neuroscience Letters ·C. Allard, Lionel Carneiro, Stephan C. Collins, (unknown), (unknown), Luc Pénicaud, Corinne Leloup	12
10	Chronic palmitate exposure inhibits insulin secretion by dissociation of Ca2+ channels from secretory granules (Cell Metabolism) 2011 ·Cell Metabolism ·Michael B. Hoppa, Stephan C. Collins, Reshma Ramracheya, Leanne Hodson, Stefan Amisten, (unknown), Paul Johnson, F M Ashcroft, Patrik Rorsman	2
11	miR-375 maintains normal pancreatic α- and β-cell mass breakdown → 2009 ·Proceedings of the National Academy of Sciences ·Matthew N. Poy, Jean Hausser, Mirko Trajkovski, Matthias Braun, Stephan C. Collins, Patrik Rorsman, Mihaela Zavolan, Markus Stoffel	617
12	Suppression of Sulfonylurea- and Glucose-Induced Insulin Secretion In Vitro and In Vivo in Mice Lacking the Chloride Transport Protein ClC-3 2009 ·Cell Metabolism ·Daiqing Li, Xingjun Jing, Albert Salehi, Stephan C. Collins, Michael B. Hoppa, Anders H. Rosengren, Enming Zhang, Ingmar Lundquist, Charlotta S. Olofsson, Matthias Mörgelin, Lena Eliasson, Patrik Rorsman, Erik Renström	40
13	Regulation of PKD by the MAPK p38δ in Insulin Secretion and Glucose Homeostasis 2009 ·Cell ·Grzegorz Sumara, Ivan Formentini, Stephan C. Collins, Izabela Sumara, Renata Windak, Bernd Bodenmiller, Reshma Ramracheya, Dorothée Caille, Huiping Jiang, Kenneth A. Platt, Paolo Meda, Ruedi Aebersold, Patrik Rorsman, Roméo Ricci	198
14	A mouse model of neonatal diabetes caused by the K-ATP channel mutation Kir6.2-V59M 2008 ·Diabetologia ·Christiane Girard, Thomas F. Wunderlich, (unknown), Stephan C. Collins, (unknown), Peter Proks, Fernando Abdulkader, Adrian J. L. Clark, Liz Bentley, Juris Galvanovskis, Roger Cox, Patrik Rorsman, Jens C. Brüning, F M Ashcroft	3
15	Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic β cells recapitulates neonatal diabetes 2008 ·Journal of Clinical Investigation ·Christophe A. Girard, F. Thomas Wunderlich, Kenju Shimomura, Stephan C. Collins, (unknown), Peter Proks, Fernando Abdulkader, Anne Clark, Vicky Ball, Lejla Zubcevic, Liz Bentley, Rebecca Clark, (unknown), Alison Hugill, Juris Galvanovskis, Roger Cox, Patrik Rorsman, Jens C. Brüning, Frances M. Ashcroft	89
16	Long-term exposure of mouse pancreatic islets to oleate or palmitate results in reduced glucose-induced somatostatin and oversecretion of glucagon 2008 ·Diabetologia ·Stephan C. Collins, Albert Salehi, Lena Eliasson, Charlotta S. Olofsson, Patrik Rorsman	32
17	Adiponectin receptor genes: mutation screening in syndromes of insulin resistance and association studies for type 2 diabetes and metabolic traits in UK populations 2007 ·Diabetologia ·Stephan C. Collins, Jian’an Luan, (unknown), Allan Daly, Robert K. Semple, Stephen O’Rahilly, Nicholas J. Wareham, Inês Barroso	21
18	Mapping diabetes QTL in an intercross derived from a congenic strain of the Brown Norway and Goto-Kakizaki rats 2006 ·Mammalian Genome ·Stephan C. Collins, Robert H. Wallis, Steven P. Wilder, Karin J. Wallace, Karène Argoud, Pamela J. Kaisaki, Marie‐Thérèse Bihoreau, Dominique Gauguier	12
19	Enhanced insulin secretion and cholesterol metabolism in congenic strains of the spontaneously diabetic (Type 2) Goto Kakizaki rat are controlled by independent genetic loci in rat chromosome 8 2004 ·Diabetologia ·Robert H. Wallis, Karin J. Wallace, Stephan C. Collins, Martina A. McAteer, Karène Argoud, Marie Thérèse Bihoreau, Pamela J. Kaisaki, Dominique Gauguier	25
20	Detailed Comparative Gene Map of Rat Chromosome 1 with Mouse and Human Genomes and Physical Mapping of an Evolutionary Chromosomal Breakpoint 2000 ·Genomics ·Pamela J. Kaisaki, Mathias Rouard, Patrick Danoy, Robert H. Wallis, Stephan C. Collins, (unknown), Elaine R. Levy, Mark Lathrop, Marie‐Thérèse Bihoreau, Dominique Gauguier	14

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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