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1. Full Text High-throughput discovery of novel developmental phenotypes
by Dickinson, Mary E and Ji, Xiao and Teboul, Lydia and Wong, Michael D and White, Jacqueline K and Meehan, Terrence F and Westerberg, Henrik and Adissu, Hibret and Baker, Candice N and Brianna Caddle, L and Chiani, Francesco and Clary, Dave and Cleak, James and Daly, Mark J and Denegre, James M and Edie, Sarah M and Gailus-Durner, Valerie and Galli, Antonella and Gambadoro, Alessia and Gallegos, Juan and Johnson, Sara J and Lawson, Thomas N and Lek, Monkol and Mason, Jeremy and McElwee, Melissa L and Nutter, Lauryl M.J and Rowland, Douglas J and Samocha, Kaitlin E and Seavitt, John R and Szoke-Kovacs, Zsombor and Trainor, Amanda G and Wakana, Shigeharu and Warren, Jonathan and West, David B and Tocchini-Valentini, Glauco P and Flicek, Paul and Bradley, Allan and Skarnes, William C and Justice, Monica J and Parkinson, Helen E and Moore, Mark and Wells, Sara and Svenson, Karen L and Herault, Yann and Mallon, Ann-Marie and Mark Henkelman, R and Brown, Steve D.M and Adams, David J and Kent Lloyd, K.C and McKerlie, Colin and Urban, Barbara and Lund, Caroline and LaCasse, Taylor and Mehalow, Adrienne and Taft, Robert and Kutney, Peter and Goodwin, Leslie and Kales, Susan and Urban, Rachel and Palmer, Kristina and Pertuy, Fabien and Bitz, Deborah and Weber, Bruno and Jacobs, Hughes and Ennah, Hamid and Ali-Hadji, Dalila and Wattenhofer-Donze, Marie and André, Philippe and Birling, Marie-Christine and Pavlovic, Guillaume and Sorg, Tania and Morse, Iva and Benso, Frank and Harrison, Jackie and Guo, Ruolin and Qu, Dawei and Spring, Shoshana and Ellegood, Jacob and Shang, Xueyuan and Feugas, Pat and Creighton, Amie and Penton, Patricia Castellanos and Danisment, Ozge and Griggs, Nicola and Tudor, Catherine L and Green, Angela L and Icoresi Mazzeo, Cecilia and Siragher, Emma and Lillistone, Charlotte and Gleeson, Diane and Sethi, Debarati and Bayzetinova, Tanya and Burvill, Jonathan and Habib, Bishoy and Maswood, Ryea and Woods, Michael and Grau, Evelyn and Sinclair, Caroline and Brown, Ellen and Ayabe, Shinya and Int Mouse Phenotyping Consortium and The International Mouse Phenotyping Consortium
Nature (London), ISSN 0028-0836, 09/2016, Volume 537, Issue 7621, pp. 508 - 514
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic research | Phenotype | Research | High-throughput screening (Biochemical assaying) | Methods | Genotype & phenotype | Disease | Developmental biology | Genes | Genomes | Mutation | Embryos | Index Medicus | knockout | embryonic lethal | mouse | KOMP | IMPC | EUCOMM
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2. Full Text New models for human disease from the International Mouse Phenotyping Consortium
by Cacheiro, Pilar and Haendel, Melissa A and Smedley, Damian and Meehan, Terrence and Mason, Jeremy and Mashhadi, Hamed Haseli and Muñoz-Fuentes, Violeta and Tocchini, Glauco and Lloyd, Kent K. C and McKerlie, Colin and Bower, Lynette and Clary, Dave and Nutter, Lauryl M. J and Flenniken, Ann M and Teboul, Lydia and Codner, Gemma and Wells, Sara and Herault, Yann and Sorg, Tania and Vasseurm, Laurent and Selloum, Mohammed and Roux, Michel and Jacobs, Hugues and Meziane, Hamid and Champy, Marie-France and About, Ghina Bou and Murray, Steve and Chesler, Elissa and Kumar, Vivek and White, Jacqui and Braun, Robert E and Beaudet, Arthur L and Dickinson, Mary E and Heaney, Jason D and Lorenzo, Isabel and Lanza, Denise G and Reynolds, Corey L and Ward, Christopher S and Samaco, Rodney C and Veeraragavan, Surabi and Hsu, Chih-Wei and Christianson, Audrey E and Gallegos, Juan J and Seavitt, John Richard and Gaspero, Angelina and Green, Jennie R and Garza, Garza and Garza, Arturo and Bohat, Ritu and Sedlacek, Radislav and Brown, Steve D. M and Int Mouse Phenotyping Consortium M and International Mouse Phenotyping Consortium and the Monarch Initiative and the International Mouse Phenotyping Consortium and the Monarch Initiative
Mammalian genome, ISSN 0938-8990, 2019, Volume 30, Issue 5-6, pp. 143 - 150
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Medical colleges | Analysis | Genes | Genomics | Consortia | Phenotypes | Disease | Precision medicine | Rodents | Phenotyping | Genomes | Mimicry | Index Medicus | Life Sciences | Genetics
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3. Full Text Prevalence of sexual dimorphism in mammalian phenotypic traits
by Mason, Jeremy and Brown, Steve D.M and Flenniken, Ann M and Fuchs, Helmut and de Angelis, Martin Hrabe and Guo, Shiying and Greenaway, Simon and Heller, Ruth and Herault, Yann and Kurbatova, Natalja and Lloyd, K.C. Kent and Masuya, Hiroshi and Mott, Richard F and Murray, Stephen A and Parkinson, Helen and Ramirez-Solis, Ramiro and Seavitt, John R and Smedley, Damian and Speak, Anneliese O and Steel, Karen P and Svenson, Karen L and Wakana, Shigeharu and Westerberg, Henrik and Tamura, Masaru and Kaneda, Hideki and Furuse, Tamio and Kobayashi, Kimio and Yamada, Ikuko and Tanaka, Nobuhiko and Schuchbauer, Michael A and Tolentino, Todd and Vukobradovic, Igor and Owen, Celeste and Qu, Dawei and Morikawa, Lily and Law, Napoleon and Shang, Xueyuan and Feugas, Patricia and Eskandarian, Mohammad and Nutter, Lauryl M.J and Sohel, Khondoker and Miller, David and Clark, Greg and Cabezas, Jorge and Tondat, Sandra and Macmaster, Suzanne and Gertsenstein, Marina and Fray, Martin and Caulder, Adam and Loeffler, Jorik and Cleak, James and Johnson, Sara and Szoke-Kovacs, Zsombor and Mianne, Joffrey and Allen, Susan and Stewart, Michelle and Sinclair, Caroline and Brown, Ellen and Doe, Brendan and Woods, Mike and Kundi, Helen and Griffiths, Mark N.D and Kipp, Christian and Melvin, David G and Alcantara, Rafael and Galli, Antonella and Tudor, Catherine L and Green, Angela L and Kussy, Fiona L and Tuck, Elizabeth J and Siragher, Emma J and Vancollie, Valerie E and Gates, Amy S and Sanderson, Mark and Shannon, Carl and Sumowski, Maksymilian T and Swiatkowska, Agnieszka and Mazzeo, Cecilia Icoresi and Dabrowska, Monika H and Estabel, Jeanne and Marie, Wattenhofer-Donze and Ali-Hadji, Dalila and Charles, Philippe and Le Marchand, Elise and Moreth, Kristin and Stoeger, Tobias and Wurst, Wolfgang and Bekeredjian, Raffi and Ollert, Markus and Calzada-Wack, Julia and Steinkamp, Ralph and Lengger, Christoph and Östereicher, Manuela A and Maier, Holger and Zimprich, Annemarie and Bürger, Antje and Zimmer, Andreas and Wolf, Eckhard and Klingenspor, Martin and Schmidt-Weber, Carsten and Int Mouse Phenotyping Consortium and International Mouse Phenotyping Consortium
Nature communications, ISSN 2041-1723, 06/2017, Volume 8, Issue 1, pp. 15475 - 15475
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Phenotype | Animals | Body Weight | Quantitative Trait, Heritable | Mammals - physiology | Female | Genotype | Mice | Genes, Modifier | Sex Characteristics | Genotype & phenotype | Animal models | Biological effects | Sex | Dimorphism | Sexual dimorphism | Mammals | Mutants | Index Medicus
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4. Full Text Disease model discovery from 3,328 gene knockouts by the International Mouse Phenotyping Consortium
by Meehan, Terrence F and Conte, Nathalie and West, David B and Jacobsen, Julius O and Mason, Jeremy and Warren, Jonathan and Chen, Chao-Kung and Tudose, Ilinca and Relac, Mike and Matthews, Peter and Karp, Natasha and Santos, Luis and Fiegel, Tanja and Ring, Natalie and Westerberg, Henrik and Greenaway, Simon and Sneddon, Duncan and Morgan, Hugh and Codner, Gemma F and Stewart, Michelle E and Brown, James and Horner, Neil and Haendel, Melissa and Washington, Nicole and Mungall, Christopher J and Reynolds, Corey L and Gallegos, Juan and Gailus-Durner, Valerie and Sorg, Tania and Pavlovic, Guillaume and Bower, Lynette R and Moore, Mark and Morse, Iva and Gao, Xiang and Tocchini-Valentini, Glauco P and Obata, Yuichi and Cho, Soo Young and Seong, Je Kyung and Seavitt, John and Beaudet, Arthur L and Dickinson, Mary E and Herault, Yann and Wurst, Wolfgang and De Angelis, Martin Hrabe and Kent Lloyd, K.C and Flenniken, Ann M and Nutter, Lauryl M J and Newbigging, Susan and McKerlie, Colin and Justice, Monica J and Murray, Stephen A and Svenson, Karen L and Braun, Robert E and White, Jacqueline K and Bradley, Allan and Flicek, Paul and Wells, Sara and Skarnes, William C and Adams, David J and Parkinson, Helen and Mallon, Ann-Marie and Brown, Steve D.M and Smedley, Damian and Int Mouse Phenotyping Consortium and International Mouse Phenotyping Consortium and The International Mouse Phenotyping Consortium
Nature genetics, ISSN 1061-4036, 08/2017, Volume 49, Issue 8, pp. 1231 - 1238
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Phenotype | Animals | Humans | Female | Genetic Diseases, Inborn | Male | Mice | Gene Knockout Techniques | Disease Models, Animal | Mice, Knockout | Usage | Genetic aspects | Research | Animal models in research | Genomics | Heart | Animal models | Ontology | Disease | Genes | Disorders | Genomes | Statistical methods | Gene sequencing | Consortia | Signal transduction | Annotations | Databases | Rodents | Right ventricular dysplasia | Automation | Gene expression | Ventricular dysplasia | Diseases | Studies | Acids | Phenotyping | Diagnostic systems | Mutation | Ventricle | Index Medicus
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5. Full Text A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
by Santos, Luis and Mason, Jeremy and Pearson, Selina and Bower, Lynette R and Meziane, Hamid and Kelsey, Lois and Allen, Sue and Clementson-Mobbs, Sharon and Fray, Martin and Joynson, Russell and Kenyon, Janet and Parker, Andrew and Stewart, Michelle and Walling, Alison and Matthews, Peter and Relac, Mike and El Fertak, Leila and Ennah, Hamid and Ali-Hadji, Dalila and Ayadi, Abdel and Wattenhofer-Donze, Marie and Moulaert, David and André, Philippe and Pavlovic, Guillaume and Lux, Aline and Bour, Raphael and Bam'Hamed, Chaouki and Leblanc, Sophie and Selloum, Mohammed and Kaneda, Hideki and Kobayashi, Kimio and Miura, Ikuo and Obata, Yuichi and Suzuki, Tomohiro and Tanaka, Nobuhiko and Yamada, Ikuko and Yoshiki, Atsushi and Berberovic, Zorana and Bubshait, Mohammed and Clark, Greg and Clarke, Shannon and Eskandarian, Mohammad and Feugas, Patricia and Laurin, Valerie and MacMaster, Sue and Morikawa, Lily and Newbigging, Susan and Shang, Xueyuan and Tondat, Sandra and Vukobradovic, Igor and Zhu, Yingchun and Chiani, Francesco and Di Pietro, Chiara and Di Segni, Gianfranco and Ermakova, Olga and Gambadoro, Aalessia and Golini, Elisabetta and Sala, Gina La and Mandillo, Silvia and Pasquini, Miriam and Rossi, Nicoletta and Scavizzi, Ferdinando and Tocchini-Valentini, Giuseppe D and Beig, Joachim and Bürger, Antje and Graw, Jochen and Schick, Joel and Amarie, Oana and Garrett, Lillian and Zimprich, Annemarie and Aguilar-Pimentel, Antonio and Calzada-Wack, Julia and Moreth, Kristin and Östereicher, Manuela A and Treise, Irina and Eickelberg, Oliver and Becker, Lore and Klopstock, Thomas and Ollert, Markus and Zimmer, Andreas and Rathkolb, Birgit and Klingenspor, Martin and Gao, Xiang and Skarnes, William C and Dickinson, Mary E and Wurst, Wolfgang and De Angelis, Martin Hrabe and Herault, Yann and Wakana, Shigeharu and Murray, Stephen A and Braun, Robert E and Adams, David J and Smedley, Damian and Meehan, Terrence F and Parkinson, Helen E and Teboul, Lydia M and Wells, Sara and Steel, Karen P and Mallon, Ann-Marie and Brown, Steve D. M and Int Mouse Phenotyping Consortium and International Mouse Phenotyping Consortium and The International Mouse Phenotyping Consortium
Nature communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 886 - 11
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Hearing Loss - genetics | Phenotype | Animals | Datasets as Topic | Genetic Testing | Protein Interaction Maps - genetics | Hearing Loss - epidemiology | Mice | Hearing Tests | Mice, Knockout | Consortia | Genes | Phenotyping | Auditory system | Hearing protection | Hearing impairment | Hearing loss | Index Medicus
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6. Full Text A population study of common ocular abnormalities in C57BL/6N rd8 mice
by Moore, Bret A and Roux, Michel J and Sebbag, Lionel and Cooper, Ann and Edwards, Sydney G and Leonard, Brian C and Imai, Denise M and Griffey, Stephen and Bower, Lynette and Clary, Dave and Lloyd, K. C. Kent and Hérault, Yann and Thomasy, Sara M and Murphy, Christopher J and Moshiri, Ala
Investigative ophthalmology & visual science, ISSN 0146-0404, 05/2018, Volume 59, Issue 6, pp. 2252 - 2261
Knockout animals | Optical coherence tomography | Genetic diseases | Morphometry | Mouse models | Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Index Medicus | Life Sciences | Animal genetics | Human health and pathology | Genetics | Sensory Organs | mouse models | genetic diseases | knockout animals | optical coherence tomography | Anatomy and Pathology | Oncology | morphometry
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7. Full Text Identification of genetic elements in metabolism by high-throughput mouse phenotyping
by Rozman, Jan and Schütt, Christine and Sharma, Sapna and Kistler, Martin and Aguilar-Pimentel, Antonio and Treise, Irina and Hölter, Sabine M and Brachthäuser, Laura and Zapf, Lilly and Cho, Yi-Li and Da Silva-Buttkus, Patricia and Tudose, Ilinca and Relac, Mike and Matthews, Peter and Natukunda, Helen P and Cleak, James and Teboul, Lydia M and Clementson-Mobbs, Sharon and Szoke-Kovacs, Zsombor and Johnson, Sara J and Stewart, Michelle E and Steel, Karen P and Dench, Joshua and Lafont, David and Vancollie, Valerie E and Pearson, Selina A and Sanderson, Mark and Shannon, Carl and Anthony, Lauren F. E and Doe, Brendan and Galli, Antonella and Swiatkowska, Agnieszka and Isherwood, Christopher M and Maguire, Anna Karin B and Adams, David J and Bottomley, Joanna and Ryder, Ed and Pouilly, Laurent and Ayadi, Abdel and Selloum, Mohammed and Wood, Joshua A and Havel, Peter and Tolentino, Todd and Trainor, Amanda and Djan, Esi and Huynh, Alison and De Vera, Vincent and Garza, Arturo and Lazo, Iride and Bohat, Ritu and Kalaga, Sowmya and Qu, Dawei and Guo, Ruolin and Newbigging, Susan and Law, Napoleon and Shang, Xueyuan and Wang, Yanchun and Laurin, Valerie and Clarke, Shannon and Jacob, Elsa and Pereira, Monica and Hunter, Jane and Clark, Greg and Ganguly, Milan and Ermakova, Olga and Golini, Elisabetta and Marazziti, Daniela and Tocchini-Valentini, Giuseppe D and Suzuki, Tomohiro and Yoshiki, Atsushi and Chambers, J. Nicole and Beig, Joachim and Kühn, Ralf and Schick, Joel and Giesert, Florian and Graw, Jochen and Ollert, Markus and Schmidt-Weber, Carsten and Stoeger, Tobias and Önder Yildirim, Ali and Klopstock, Thomas and Bekeredjian, Raffi and Zimmer, Andreas and Smedley, Damian and Kim, Hyoung-Chin and Mallon, Ann-Marie and Wells, Sara and Lelliott, Christopher J and White, Jacqueline K and Champy, Marie-France and Reynolds, Corey L and Flenniken, Ann M and Nutter, Lauryl M. J and Dobbie, Michael S and Kent Lloyd, K.C and Flicek, Paul and Sedlacek, Radislav and Wang, Chi-Kuang Leo and Wurst, Wolfgang and Häring, Hans-Ulrich and IMPC Consortium
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 288 - 16
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study | Basal Metabolism - genetics | Area Under Curve | Diabetes Mellitus, Type 2 - genetics | Humans | Gene Regulatory Networks | Body Weight - genetics | Obesity - genetics | Mice, Knockout | Triglycerides - metabolism | Phenotype | Animals | High-Throughput Screening Assays | Oxygen Consumption - genetics | Metabolic Diseases - genetics | Mice | Blood Glucose - metabolism | Consortia | Annotations | Genes | Phenotyping | Data processing | Genomes | Regulatory sequences | Genetic factors | Metabolism | Binding sites | Metabolic disorders | Index Medicus
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