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Author Details

Ann M Flenniken
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
1980
56
27
PMIDPaper TitleJournal TitlePublished Year
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37628590The <i>ATP6V1B2</i> DDOD/DOORS-Associated p.Arg506* Variant Causes Hyperactivity and Seizures in Mice.Genes (Basel)2023
37623890Sexual Dimorphism of the Mouse Plasma Metabolome Is Associated with Phenotypes of 30 Gene Knockout Lines.Metabolites2023
34328547INFRAFRONTIER quality principles in systemic phenotyping.Mamm Genome2022
35552317Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.Pain2022
33230005Cage-lid hanging behavior as a translationally relevant measure of pain in mice.Pain2021
34050187Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma.NPJ Syst Biol Appl2021
33151080Process and Workflow for Preparation of Disparate Mouse Tissues for Proteomic Analysis.J Proteome Res2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
32542000The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities.PLoS One2020
30854487Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Commun Biol2019
31121816A Comprehensive Plasma Metabolomics Dataset for a Cohort of Mouse Knockouts within the International Mouse Phenotyping Consortium.Metabolites2019
29348434Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Nat Commun2018
30100824The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation.Conserv Genet2018
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
29026089A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Nat Commun2017
29144450Corrigendum: High-throughput discovery of novel developmental phenotypes.Nature2017
28650954Prevalence of sexual dimorphism in mammalian phenotypic traits.Nat Commun2017
27626380High-throughput discovery of novel developmental phenotypes.Nature2016
25992600Applying the ARRIVE Guidelines to an In Vivo Database.PLoS Biol2015
26214591Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Nat Genet2015
24443344First mouse model for combined osteogenesis imperfecta and Ehlers-Danlos syndrome.J Bone Miner Res2014
25202984A lymphatic defect causes ocular hypertension and glaucoma in mice.J Clin Invest2014
23874215ENU-induced mutation in the DNA-binding domain of KLF3 reveals important roles for KLF3 in cardiovascular development and function in mice.PLoS Genet2013
24086539Enu mutagenesis identifies a novel platelet phenotype in a loss-of-function Jak2 allele.PLoS One2013
21924221Cytopenia induction by 5-fluorouracil identifies thrombopoietic mutants in sensitized ENU mutagenesis screens.Exp Hematol2012
22573557A novel Phex mutation in a new mouse model of hypophosphatemic rickets.J Cell Biochem2012
21193012A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.Exp Hematol2011
21305608The V-ATPase a3 subunit mutation R740S is dominant negative and results in osteopetrosis in mice.J Bone Miner Res2011
21209254The Sweet Pee model for Sglt2 mutation.J Am Soc Nephrol2011
20503384The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling.Dev Dyn2010
17699753Feedback regulation of p38 activity via ATF2 is essential for survival of embryonic liver cells.Genes Dev2007
16410543Anatomical phenotyping in the brain and skull of a mutant mouse by magnetic resonance imaging and computed tomography.Physiol Genomics2006
15854131Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia.Exp Dermatol2005
16155213A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.Development2005
12480926Efficient germline transmission of mouse embryonic stem cells grown in synthetic serum in the absence of a fibroblast feeder layer.Lab Invest2002
9425139Segmental expression of the EphA4 (Sek-1) receptor tyrosine kinase in the hindbrain is under direct transcriptional control of Krox-20.Development1998
9321688Roles of Eph receptors and ephrins in neural crest pathfinding.Cell Tissue Res1997
8755474Eph receptors and ligands comprise two major specificity subclasses and are reciprocally compartmentalized during embryogenesis.Neuron1996
8971342Cell-cell interactions and segmentation in the developing vertebrate hindbrain.Biochem Soc Symp1996
8903354Distinct and overlapping expression patterns of ligands for Eph-related receptor tyrosine kinases during mouse embryogenesis.Dev Biol1996
8808709Elk-L3, a novel transmembrane ligand for the Eph family of receptor tyrosine kinases, expressed in embryonic floor plate, roof plate and hindbrain segments.Oncogene1996
8117616Expression of the Wilms' tumor suppressor gene WT1 during mouse embryogenesis.Cell Growth Differ1993
1335280Coordinate expression of Wilms' tumor genes correlates with Wilms' tumor phenotypes.Cell Growth Differ1992
1480037Regulation of TIMP gene expression in cell culture and during mouse embryogenesis.Matrix Suppl1992
1908771Localization of TIMP in cycling mouse hair.Development1991
1849903Identification of a serum- and phorbol ester-responsive element in the murine tissue inhibitor of metalloproteinase gene.J Biol Chem1991
2120112Developmental expression of the endogenous TIMP gene and a TIMP-lacZ fusion gene in transgenic mice.Genes Dev1990
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Collaborators

Colin McKerlie
The Hospital for Sick Children
Co-authored papers 23
Kent C Lloyd
University of California davis
Co-authored papers 17
Lauryl M J Nutter
The Hospital for Sick Children
Co-authored papers 17
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 16
Ann-Marie Mallon
The Turing Institute
Co-authored papers 15
Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 14
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers 14
Sara Wells
Mary Lyon Centre at Medical Research Council
Co-authored papers 14
Jacqueline K White
Wellcome Trust Sanger Institute
Co-authored papers 13
Helen Parkinson
European Bioinformatics Institute
Co-authored papers 13
Terrence F Meehan
European Bioinformatics Institute
Co-authored papers 12
Janet Rossant
The Hospital for Sick Children
Co-authored papers 12
Jeremy Mason
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 11
John R Seavitt
Baylor College of Medicine
Co-authored papers 11
Anne M Dickinson
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 11
Tania Sorg
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 10
Stephen A Murray
Columbia University.
Co-authored papers 10
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 9
Robert E Braun
University of Maine
Co-authored papers 9
Paul Flicek
European Bioinformatics Institute
Co-authored papers 9
Lynette Bower
University of California davis
Co-authored papers 9
Bryan R G Williams
Co-authored papers 9
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 9
Karen L Svenson
Co-authored papers 9
Wolfgang Wurst
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 8
Luis Santos
The Turing Institute
Co-authored papers 8
Xiang Gao
Nanjing Biomedical Research Institute, Nanjing University
Co-authored papers 8
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
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David B West
Children's Hospital Oakland Research Institute
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Arthur L Beaudet
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Release 1.2