부산대학교 도서관

Grodin, Erica N.; Kirsch, Dylan E.; Nieto, Steven; Belnap, Malia; Castillo, Yenashi; Baker, Nirvana; Wassum, Kate M.; Grant, Kathleen A.; Ray, Lara A.

Drug and Alcohol Dependence. 274

Abigail E. Powell; Hannah Caruso; Soyoon Park; Jui-Lin Chen; Jessica O’Rear; Brian J. Ferrer; Daniel J. Stieh; Adam M. Weiss; David M. Belnap; Audrey Walker; Anneliese Bruening; Airn Hartwig; Kaitlin R. Sprouse; Amin Addetia; Abeer N. Alshukairi; Vida Ahyong; Cristy S. Dougherty; David Veesler; Richard Bowen; Julie E. Ledgerwood; Michael S. Kay; Payton A.-B. Weidenbacher; Brad A. Palanski

Nature Communications, Vol 17, Iss 1 (2026)

Belnap, Malia A.. Neuroscience Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, US; Kirsch, Dylan E.. Department of Psychology, University of California, Los Angeles, Los Angeles, CA, US; Grodin, Erica N.. Department of Psychology, University of California, Los Angeles, Los Angeles, CA, US; Ray, Lara A.. ORCID 0000-0002-5734-9444. Department of Psychology, University of California, Los Angeles, Los Angeles, CA, US

Exp Clin Psychopharmacol

McManus, Kaitlin R.; Belnap, Malia; Kirsch, Dylan E.; Ray, Lara A.; Grodin, Erica N.

Drug and Alcohol Dependence. 268

Belnap, N.; Müller, T.; Placek, T.

Studia Logica: An International Journal for Symbolic Logic, 2021 Apr 01. 109(2), 239-284.

Analysis. Oct2002, Vol. 62 Issue 4, p330-336. 7p.

Edward N. Wilson; Christina B. Young; Javier Ramos Benitez; Michelle S. Swarovski; Igor Feinstein; Manu Vandijck; Yann Le Guen; Nandita M. Kasireddy; Marian Shahid; Nicole K. Corso; Qian Wang; Gabriel Kennedy; Alexandra N. Trelle; Betty Lind; Divya Channappa; Malia Belnap; Veronica Ramirez; Irina Skylar-Scott; Kyan Younes; Maya V. Yutsis; Nathalie Le Bastard; Joseph F. Quinn; Christopher H. van Dyck; Angus Nairn; Carolyn A. Fredericks; Lu Tian; Geoffrey A. Kerchner; Thomas J. Montine; Sharon J. Sha; Guido Davidzon; Victor W. Henderson; Frank M. Longo; Michael D. Greicius; Anthony D. Wagner; Tony Wyss-Coray; Kathleen L. Poston; Elizabeth C. Mormino; Katrin I. Andreasson

Alzheimer’s Research & Therapy, Vol 14, Iss 1, Pp 1-12 (2022)

Italo Linfante; Wayne Clark; Diogo C. Haussen; Ricardo Hanel; Rwoof Reshi; Guilherme Dabus; Ronald Jubin; Mona P. Roshan; Star Belnap; Thanh N. Nguyen; James Grotta; Robert Wicks; Marilyn J. Cipolla; David S. Liebeskind; Raul G. Nogueira

Stroke: Vascular and Interventional Neurology, Vol 4, Iss 4 (2024)

Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Prakash S; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.; Kerkhof J; Verspeeten Clinical Genome Center, London Health Sciences Center, London, ON N6A 5W9, Canada.; Sadikovic B; Verspeeten Clinical Genome Center, London Health Sciences Center, London, ON N6A 5W9, Canada.; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 5C1, Canada.; White S; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC 3052, Australia.; Department of Paediatrics, Univerwsity of Melbourne, Melbourne, VIC 3010, Australia.; Naymik M; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Sloan J; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Bonfitto A; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Belnap N; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Sanchez-Castillo M; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Jepsen W; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Huentelman M; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Bernes S; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.; Narayanan V; Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.; Kaur S; Phoenix Children's Hospital, Phoenix, AZ 85016, USA.; Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ 85004, USA.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

Craig, Andrew; Davey, Brian A.; Haviar, Miroslav

Xiaobing Zhou; Hilda Smith; Ana Giraldo Silva; Jayne Belnap; Ferran Garcia-Pichel

PLoS ONE, Vol 11, Iss 10, p e0164932 (2016)

Craig, Andrew; Davey, Brian A.; Haviar, Miroslav

Zanoni P; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich, Switzerland. paolo.zanoni@uzh.ch.; Steindl K; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich, Switzerland.; Sengupta D; Department of Biology, Stanford University, Stanford, CA, USA.; Joset P; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich, Switzerland.; Bahr A; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich, Switzerland.; Sticht H; Institute of Biochemistry, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.; Lang-Muritano M; Department of Pediatric Endocrinology and Diabetology, University Children's Hospital, Zurich, Switzerland.; Children's Research Centre, University Children's Hospital, Zurich, Switzerland.; van Ravenswaaij-Arts CMA; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.; Shinawi M; Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO, USA.; Andrews M; Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO, USA.; Attie-Bitach T; Service d'Histologie-Embryologie-Cytogénétique, Unité d'Embryofoetopathologie, Hôpital Necker-Enfants Malades, APHP, Paris, France.; INSERM UMR 1163, Université de Paris, Imagine Institute, Paris, France.; Maystadt I; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Faculté de médecine, Université de Namur, Namur, Belgium.; Belnap N; Center for Rare Childhood Disorders (C4RCD), Translational Genomics Research Institute, Phoenix, AZ, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.; Benoit V; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Département de Biologie Moléculaire, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Delplancq G; Centre de Génétique Humaine, Université de Franche-Comté, CHU, Besançon, France.; Service de Neuropédiatrie, CHU, Besançon, France.; de Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Grotto S; Maternité Port-Royal, AP-HP, Hôpital Cochin, Paris, France.; Lacombe D; Service de Génétique Médicale, Hôpital Pellegrin CHU, Bordeaux, France.; Larson A; Department of Pediatrics, Section of Genetics, University of Colorado Anschutz Medical Campus, Denver, CO, USA.; Mourmans J; Deventer Ziekenhuis, Deventer, the Netherlands.; Õunap K; Department of Clinical Genetics, United Laboratories, Tartu University Hospital, Tartu, Estonia.; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Petrilli G; Service d'Histologie-Embryologie-Cytogénétique, Unité d'Embryofoetopathologie, Hôpital Necker-Enfants Malades, APHP, Paris, France.; Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Ramsey K; Center for Rare Childhood Disorders (C4RCD), Translational Genomics Research Institute, Phoenix, AZ, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.; Blok LS; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Tsatsaris V; Maternité Port-Royal, AP-HP, Hôpital Cochin, Paris, France.; Vitobello A; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD, FHU-TRANSLAD, Unité Fonctionnelle D'Innovation en Diagnostique Génomique Des Maladies Rares, Pôle de Biologie, CHU Dijon Bourgogne, Dijon, France.; Faivre L; Centre de Référence Maladies Rares « Anomalies du Développement Et Syndrome Malformatifs » de L'Est, Hôpital D'Enfants, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Wheeler PG; Division of Genetics, Arnold Palmer Hospital, Orlando Health, Orlando, FL, USA.; Wevers MR; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Wojcik M; Department of Pediatrics, Boston Children's Hospital, Divisions of Newborn Medicine and Genetics and Genomics, Boston, MA, USA.; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Zweier M; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich, Switzerland.; Gozani O; Department of Biology, Stanford University, Stanford, CA, USA.; Rauch A; Institute of Medical Genetics, University of Zürich, Schlieren-Zurich, Switzerland. anita.rauch@medgen.uzh.ch.; Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland. anita.rauch@medgen.uzh.ch.; Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland. anita.rauch@medgen.uzh.ch.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Z. T. Aanderud; T. B. Smart; N. Wu; A. S. Taylor; Y. Zhang; J. Belnap

Biogeosciences, Vol 15, Pp 3831-3840 (2018)

Mathematical Logic Quarterly. 1995, Vol. 41 Issue 4, p442-454. 13p.

Andrew Craig; Brian Davey; Miroslav Haviar

Categories and General Algebraic Structures with Applications, Vol 17, Iss 1, Pp 47-84 (2022)

PHILOSOPHY AND PHENOMENOLOGICAL RESEARCH; SEP 1996, 56 3, p727-p730, 4p.

Belnap, N.; Ramsey, K.; Abraham, A.; Ryan, A.; Rangasamy, S.; Bonfitto, A.; Naymik, M.; Huentelman, M.; Strom, S.; Perry, D.; Subramaniam, A.; Grody, W. W.; Szelinger, S.; Narayanan, V.

Journal of Genetic Counseling (J GENETIC COUNS), Apr2025; 34(2): 1-7. (7p)

Abraham A; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Belnap N; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Szelinger S; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Jepsen W; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Balak C; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Sanchez-Castillo M; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Naymik M; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Bonfitto A; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Rangasamy S; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Kruglyak S; Element Biosciences, San Diego, California, USA.; Huentelman M; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Narayanan V; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.; Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.

Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Antoninka, Anita; Bowker, Matthew A.; Chuckran, Peter; Barger, Nichole N.; Reed, Sasha; Belnap, Jayne

Plant and Soil. August, 2018, Vol. 429 Issue 1-2, p213, 13 p.