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1. Full Text GWAS identifies four novel eosinophilic esophagitis loci
by Sleiman, Patrick M. A and Wang, Mei-Lun and Cianferoni, Antonella and Aceves, Seema and Gonsalves, Nirmala and Nadeau, Kari and Bredenoord, Albert J and Furuta, Glenn T and Spergel, Jonathan M and Hakonarson, Hakon
Nature communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, pp. 5593 - 5593
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Guanine Nucleotide Exchange Factors - genetics | Humans | Repressor Proteins - genetics | Male | STAT6 Transcription Factor - genetics | Calpain - genetics | Case-Control Studies | Adult | Female | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Eosinophilic Esophagitis - genetics | Index Medicus
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2. Full Text The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth
by Satterthwaite, Theodore D and Connolly, John J and Ruparel, Kosha and Calkins, Monica E and Jackson, Chad and Elliott, Mark A and Roalf, David R and Hopson, Ryan and Prabhakaran, Karthik and Behr, Meckenzie and Qiu, Haijun and Mentch, Frank D and Chiavacci, Rosetta and Sleiman, Patrick M.A and Gur, Ruben C and Hakonarson, Hakon and Gur, Raquel E
NeuroImage (Orlando, Fla.), ISSN 1053-8119, 01/2016, Volume 124, Issue Pt B, pp. 1115 - 1119
Neuroimaging | Development | Adolescence | Data-sharing | MRI | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Genomics | Humans | Male | Cognition | Brain - abnormalities | Brain - growth & development | Information Dissemination | Developmental Disabilities - pathology | Nervous System - growth & development | Adolescent | Female | Child Development | Internet | Child | Developmental Disabilities - psychology | Brain | Youth | Teenagers | Analysis | Child development | Phenotypes | Medical imaging | Mental disorders | Laboratories | Cognitive ability | Nervous system | Children & youth | Data dictionaries | Datasets | Mental health care | Brain research | Archives & records | Consent | Collaboration | Neurodevelopment | Psychopathology | Genotypes | Index Medicus | adolescence | development | data-sharing | neuroimaging
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3. Full Text Common variants at 5q22 associate with pediatric eosinophilic esophagitis
by Verma, Ritu and Aceves, Seema and Collins, Margaret H and Liacouras, Chris and Sherrill, Joseph D and Martin, Lisa J and Thomas, Kelly and Sleiman, Patrick M A and Spergel, Jonathan M and Franciosi, James P and Grant, Struan F A and Annaiah, Kiran and Hakonarson, Hakon and Brown-Whitehorn, Terri and Putnam, Phil E and Cianferoni, Antonella and Rothenberg, Marc E and Kim, Cecilia and Glessner, Joseph and Frackelton, Edward and Blanchard, Carine and Abonia, J Pablo and Gober, Laura and Chiavacci, Rosetta M
Nature genetics, ISSN 1061-4036, 04/2010, Volume 42, Issue 4, pp. 289 - 291
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Esophagitis - genetics | Genome-Wide Association Study | Humans | Eosinophils - pathology | Polymorphism, Single Nucleotide | Eye Proteins - genetics | Child | Cytokines - genetics | Esophagitis - pathology | Chromosomes, Human, Pair 5 | Endoscopic surgery | Usage | Genetic variation | Esophagitis | Genetic aspects | Endoscopy | Diagnosis | Research | Health aspects | Studies | Food allergies | Hospitals | Genes | Families & family life | Principal components analysis | Regression analysis | Chromosomes | Allergies | Methods | Children & youth | Index Medicus
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4. Full Text The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative
by Calkins, Monica E and Merikangas, Kathleen R and Moore, Tyler M and Burstein, Marcy and Behr, Meckenzie A and Satterthwaite, Theodore D and Ruparel, Kosha and Wolf, Daniel H and Roalf, David R and Mentch, Frank D and Qiu, Haijun and Chiavacci, Rosetta and Connolly, John J and Sleiman, Patrick M.A and Gur, Ruben C and Hakonarson, Hakon and Gur, Raquel E
Journal of child psychology and psychiatry, ISSN 0021-9630, 12/2015, Volume 56, Issue 12, pp. 1356 - 1369
neurocognition | mood | adolescents | psychosis | structure | neuroimaging | anxiety | comorbidity | children | psychopathology | young adults | public domain | genomics | behavior | Community cohort | Social Sciences | Life Sciences & Biomedicine | Psychology, Developmental | Psychiatry | Psychology | Science & Technology | Humans | Cooperative Behavior | Databases, Genetic | Genotype | Male | Neurodevelopmental Disorders - genetics | Neurodevelopmental Disorders - physiopathology | Young Adult | Phenotype | Adolescent | Adult | Female | Child | Philadelphia | Cohort Studies | Databases, Factual | Neuroimaging | Brain | Mental disorders | Genes | Assessment | Black American people | Mental health | Perceptions | Cognition | Child psychology | Recovery | Clinical assessment | Genotype & phenotype | Accuracy | Psychoses | Neuropsychology | Children | Psychopathology | Computerization | Phenotypes | Factor analysis | Behaviour | General factor | Persecution | Public domain | Fear | Interdisciplinary approach | Psychiatric disorders | Index Medicus
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5. Full Text Common genetic variants on 5p14.1 associate with autism spectrum disorders
by Schellenberg, Gerard D and Minshew, Nancy J and Korvatska, Olena and Hakonarson, Hakon and Buxbaum, Joseph D and Hutman, Ted and Alvarez Retuerto, Ana I and Sleiman, Patrick M. A and Coon, Hilary and Nurnberger, John I and Kim, Cecilia E and Pericak-Vance, Margaret A and Dong, Hongmei and Bradfield, Jonathan P and Abrahams, Brett S and Gilbert, John R and Munson, Jeffrey and Sonnenblick, Lisa I and Klin, Ami and Levy, Susan E and Herman, Edward I and Ma, Deqiong and Sakurai, Takeshi and Hou, Cuiping and Lajonchere, Clara M and Miller, Judith and Zhang, Haitao and Cook, Edwin H and Estes, Annette and Wang, Kai and State, Matthew W and Haines, Jonathan L and Sweeney, John A and Wassink, Thomas H and Ozonoff, Sally and Piven, Joseph and Chiavacci, Rosetta and Cuccaro, Michael L and Brune, Camille W and Frackelton, Edward and McMahon, William M and Geschwind, Daniel H and Takahashi, Nagahide and Owley, Thomas and Glessner, Joseph T and Salyakina, Daria and Sutcliffe, James S and Dawson, Geraldine and Bucan, Maja and Bernier, Raphael and Imielinski, Marcin and Rappaport, Eric and Sigman, Marian and Cantor, Rita M and Schultz, Robert T and Grant, Struan F. A
Nature (London), ISSN 0028-0836, 05/2009, Volume 459, Issue 7246, pp. 528 - 533
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Cell Adhesion - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Humans | Genotype | Case-Control Studies | Cell Adhesion Molecules, Neuronal - genetics | Brain - metabolism | Genetic Markers - genetics | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Cadherins - genetics | Chromosomes, Human, Pair 5 - genetics | Cohort Studies | Genetic research | Genetic aspects | Risk factors | Pervasive developmental disorders | Autism | Brain | Genomics | Quality control | Genetics | Software | Kinases | Gene expression | Chromosomes | Index Medicus
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6. Full Text ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry
by Sleiman, Patrick M.A., PhD and Annaiah, Kiran, MSc and Imielinski, Marcin, MD, PhD and Bradfield, Jonathan P., BS and Kim, Cecilia E., BA and Frackelton, Edward C., BA and Glessner, Joseph T., MSc and Eckert, Andrew W., MSc and Otieno, F. George, MSc and Santa, Erin, BA and Thomas, Kelly, BA and Smith, Ryan M., BA and Glaberson, Wendy, BA and Garris, Maria, BA and Gunnlaugsson, Sigfus, BA and Chiavacci, Rosetta M., MSc and Allen, Julian, MD and Spergel, Jonathan, MD, PhD and Grundmeier, Robert, MD, PhD and Grunstein, Michael M., MD, PhD and Magnusson, Mark, MD and Bisgaard, Hans, MD and Grant, Struan F.A., PhD and Hakonarson, Hakon, MD, PhD
Journal of allergy and clinical immunology, ISSN 0091-6749, 2008, Volume 122, Issue 6, pp. 1225 - 1227
Allergy and Immunology | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Chromosomes, Human, Pair 17 - metabolism | United States - epidemiology | Asthma - metabolism | Membrane Proteins - genetics | Humans | European Continental Ancestry Group | Male | Asthma - genetics | Chromosomes, Human, Pair 17 - genetics | Membrane Proteins - biosynthesis | Female | Polymorphism, Single Nucleotide | Asthma - epidemiology | Cohort Studies | Quantitative Trait Loci - genetics | Studies | Ratios | Genealogy | Disease | Protein folding | Genes | African Americans | Genomes | Asthma | Index Medicus | Abridged Index Medicus
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7. Full Text Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease
by Wang, Kai and Zhang, Haitao and Kugathasan, Subra and Annese, Vito and Bradfield, Jonathan P and Russell, Richard K and Sleiman, Patrick M.A and Imielinski, Marcin and Glessner, Joseph and Hou, Cuiping and Wilson, David C and Walters, Thomas and Kim, Cecilia and Frackelton, Edward C and Lionetti, Paolo and Barabino, Arrigo and Van Limbergen, Johan and Guthery, Stephen and Denson, Lee and Piccoli, David and Li, Mingyao and Dubinsky, Marla and Silverberg, Mark and Griffiths, Anne and Grant, Struan F.A and Satsangi, Jack and Baldassano, Robert and Hakonarson, Hakon
American journal of human genetics, ISSN 0002-9297, 2009, Volume 84, Issue 3, pp. 399 - 405
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | Interleukin-23 - genetics | Crohn Disease - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Signal Transduction | Interleukin-12 - genetics | Humans | Databases, Genetic | Polymorphism, Single Nucleotide | Medical research | Analysis | Genes | Genomics | Genetic research | Medicine, Experimental | Crohn's disease | Studies | Genotype & phenotype | Crohns disease | Index Medicus | Report
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8. Full Text Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
by Minshew, Nancy J and Thomas, Kelly and Nurnberger, John I and Crawford, Emily L and Otieno, Frederick and Dawson, Geraldine and Posey, David J and Annaiah, Kiran and Glaberson, Wendy and Wood, Shawn and Meyer, Kacie J and Sleiman, Patrick M. A and Miller, Judith and Munson, Jeffrey and Kim, Cecilia E and Bradfield, Jonathan P and Soorya, Latha and Frackelton, Edward C and Bucan, Maja and Sakurai, Takeshi and Hou, Cuiping and Anagnostou, Evdokia and Piven, Joseph and Schultz, Robert T and Zhang, Haitao and Cook, Edwin H and Schellenberg, Gerard D and Wang, Kai and Flory, James and Rudd, Danielle S and Sweeney, John A and Zurawiecki, Danielle and Grant, Struan F. A and Michaels, Shana and Levy, Susan E and Chiavacci, Rosetta and McMahon, William M and Brune, Camille W and Korvatska, Olena and Klei, Lambertus and Cai, Guiqing and McDougle, Christopher J and Hakonarson, Hakon and Kolevzon, Alexander and Garris, Maria and Silverman, Jeremy M and Wassink, Thomas H and Owley, Thomas and Glessner, Joseph T and Sutcliffe, James S and Reichert, Jennifer and Davis, Lea K and Bernier, Raphael and Game, Rachel M and Devlin, Bernie and Coon, Hilary and Imielinski, Marcin and Estes, Annette and Buxbaum, Joseph D
Nature (London), ISSN 0028-0836, 05/2009, Volume 459, Issue 7246, pp. 569 - 573
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Reproducibility of Results | Gene Regulatory Networks - genetics | Humans | Ubiquitin - metabolism | Genotype | Case-Control Studies | Cell Adhesion Molecules, Neuronal - genetics | Europe - ethnology | Genome, Human - genetics | Polymerase Chain Reaction | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Neurons - metabolism | Cohort Studies | Ubiquitin | Autism | Genetic aspects | Properties | Neurons | Databases | Genomics | Genes | Genetics | Standard deviation | Risk factors | Methods | Cell adhesion & migration | Index Medicus
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