Resultats de la cerca - Jeff Munson
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Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16 per Nicola H. Chapman, Annette Estes, Jeff Munson, Raphael Bernier, Sara Jane Webb, Joseph H. Rothstein, Nancy J. Minshew, Géraldine Dawson, Gerard Schellenberg, Ellen M. Wijsman
Publicat 2010Artigo -
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A Multisite Randomized Controlled Trial Comparing the Effects of Intervention Intensity and Intervention Style on Outcomes for Young Children With Autism per Sally J. Rogers, Paul J. Yoder, Annette Estes, Zachary Warren, John McEachin, Jeff Munson, Marie Rocha, Jessica Greenson, Lisa Wallace, Elizabeth Gardner, Géraldine Dawson, Catherine A. Sugar, Gerhard Hellemann, Fiona Whelan
Publicat 2020Artigo -
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Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes per Nicola H. Chapman, Alejandro Q. Nato, Raphael Bernier, Katy Ankenman, Harkirat Sohi, Jeff Munson, Ashok Patowary, Marilyn Archer, Elizabeth Blue, Sara Jane Webb, Hilary Coon, Wendy H. Raskind, Zoran Brkanac, Ellen M. Wijsman
Publicat 2015Artigo -
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Head circumference and height in autism: A study by the collaborative program of excellence in autism per Janet E. Lainhart, Erin D. Bigler, Maureen Bocian, Hilary Coon, Elena Dinh, Géraldine Dawson, Curtis K. Deutsch, Michelle Dunn, Annette Estes, Helen Tager‐Flusberg, Susan E. Folstein, Susan Hepburn, Susan Hyman, William McMahon, Nancy J. Minshew, Jeff Munson, Kathy Osann, Sally Ozonoff, Patricia M. Rodier, Sally J. Rogers, Marian Sigman, M. Anne Spence, Chris Stodgell, Fred R. Volkmar
Publicat 2006Artigo -
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Clinical characteristics of 46 pregnant women with a severe acute respiratory syndrome coronavirus 2 infection in Washington State per Erica M. Lokken, Christie L. Walker, Shani Delaney, Alisa Kachikis, Nicole M. Kretzer, Anne Erickson, Rebecca Resnick, Jeroen Vanderhoeven, Joseph Hwang, Nena Barnhart, Jasmine Rah, Stephen A. McCartney, Kimberly Kelly, Emily M. Huebner, Chad Thomas, Jessica S. Sheng, Bettina W. Paek, Kristin Retzlaff, Carolyn Kline, Jeff Munson, Michela Blain, Sylvia M. LaCourse, Gail Deutsch, Kristina M. Adams Waldorf
Publicat 2020Artigo -
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Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders per Brian J. O’Roak, Laura Vives, Wenqing Fu, Jarrett D. Egertson, Ian B. Stanaway, Ian G. Phelps, Gemma L. Carvill, Akash Kumar, Choli Lee, Katy Ankenman, Jeff Munson, Joseph B. Hiatt, Emily H. Turner, Roie Levy, Diana R. O’Day, Niklas Krumm, Bradley P. Coe, Beth Martin, Elhanan Borenstein, Deborah A. Nickerson, Heather C. Mefford, Dan Doherty, Joshua M. Akey, Raphael Bernier, Evan E. Eichler, Jay Shendure
Publicat 2012Artigo -
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Low Prevalence of Severe Acute Respiratory Syndrome Coronavirus 2 Among Pregnant and Postpartum Patients With Universal Screening in Seattle, Washington per Sylvia M. LaCourse, Alisa Kachikis, Michela Blain, LaVone E. Simmons, James A. Mays, Amber D Pattison, Carol C Salerno, Stephen A. McCartney, Nicole M. Kretzer, Rebecca Resnick, Rosemary Shay, Leah M. Savitsky, Anna Curtin, Emily M. Huebner, Kimberly Kelly, Shani Delaney, Carlos Delgado, Adrienne Schippers, Jeff Munson, Paul S. Pottinger, Seth A. Cohen, Santiago Neme, Lori Bourassa, Andrew Bryan, Alexander L. Greninger, Keith R. Jerome, Alison C. Roxby, Erica M. Lokken, Kwang‐Ting Cheng, Kristina M. Adams Waldorf, Jane Hitti
Publicat 2020Artigo -
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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder per Jillian P. Casey, Tiago R. Magalhães, Judith Conroy, Regina Regan, Naisha Shah, Richard Anney, Denis C. Shields, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Patrick Bolton, Thomas Bourgeron, S. Brennan, Phil Cali, Catarina Correia, Christina Corsello, Marc N. Coutanche, Géraldine Dawson, Maretha Jonge, Richard Delorme, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, S. Foley, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jonathan Green, Stephen J. Guter, Hákon Hákonarson, Richard Holt, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, Alexander Kolevzon, Janine A. Lamb, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Catherine Lord, Sabata C. Lund, Elena Maestrini, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Judith Miller, Fiorella Minopoli, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Gudrun Nygren, Guiomar Oliveira, Alistair T. Pagnamenta, Katerina Papanikolaou, Jeremy Parr, Barbara Parrini, Andrew Pickles, Dalila Pinto, Joseph Piven, David J. Posey, Annemarie Poustka, Fritz Poustka, Jiannis Ragoussis, Bernadette Rogé, Michael Rutter, Ana Filipa Sequeira, Latha Soorya, Inês Sousa, Nuala Sykes, Vera Stoppioni, Raffaella Tancredi, M. Tauber, Ann Thompson, Susanne Thomson, John Tsiantis, Herman Van Engeland, John B. Vincent, Fred Volkmar, Jacob Vorstman, Simon Wallace, Kai Wang, Thomas H. Wassink, Kathy White, Kirsty Wing
Publicat 2011Artigo -
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Individual common variants exert weak effects on the risk for autism spectrum disorders per Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, Jillian P. Casey, Judith Conroy, Catarina Correia, Christina Corsello, Emily L. Crawford, Maretha Jonge, Richard Delorme, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Andrew Green, Jonathan Green, Stephen J. Guter, Elizabeth A. Heron, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Suma Jacob, Graham P. Kenny, Cecilia Kim, Alexander Kolevzon, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Miriam Law-Smith, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Xiaoqing Liu, Frances Lombard, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Tiago R. Magalhães, Carine Mantoulan, Christopher J. McDougle, Nadine Melhem, Alison Merikangas, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Carolyn Noakes, Gudrun Nygren, Κaterina Papanikolaou, Alistair T. Pagnamenta, Barbara Parrini, Tara Paton, Andrew Pickles, David J. Posey, Fritz Poustka, Jiannis Ragoussis, Regina Regan, Wendy Roberts, Kathryn Roeder, Bernadette Rogé, Michael Rutter, Sabine Schlitt, Naisha Shah, Val C. Sheffield, Latha Soorya, Inês Sousa, Vera Stoppioni, Nuala Sykes, Raffaella Tancredi, Ann Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Hermán van Engeland, John B. Vincent, Fred R. Volkmar, JAS Vorstman, Simon Wallace, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, Danielle Zurawiecki, Lonnie Zwaigenbaum, Anthony Bailey
Publicat 2012Artigo -
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Functional impact of global rare copy number variation in autism spectrum disorders per Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Gary D. Bader, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, Susan E. Bryson, Andrew R. Carson, Guillermo Casallo, Jillian P. Casey, Brian Hon‐Yin Chung, Lynne Cochrane, Christina Corsello, Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Hákon Hákonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Anath C. Lionel, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge
Publicat 2010Artigo -
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A genome-wide scan for common alleles affecting risk for autism per Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Jennifer Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, N. Sykes, A. T. Pagnamenta, J.-P. de Almeida, Elena Bacchelli, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, P. F. Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, A. R. Carson, Guillermo Casallo, Jillian P. Casey, Su H. Chu, Lynne Cochrane, Christina Corsello, E. L. Crawford, A. Crossett, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, James Gilbert, Christopher Gillberg, Joseph Glessner, Joel O. Goldberg, Jonathan Green, Stephen J. Guter, Hákon Hákonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, C. Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, A. C. Lionel, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Nadine Melhem, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, C. Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Joseph Piven, David J. Posey, Annemarie Poustka, Fritz Poustka
Publicat 2010Artigo -
20
A genome-wide linkage and association scan reveals novel loci for autism per Lauren A. Weiss, Dan E. Arking, Mark J. Daly, Aravinda Chakravarti, Camille W. Brune, Kristen M. West, Ashley O’Connor, Gina M. Hilton, R Tomlinson, Andrew B. West, Edwin H. Cook, Todd Green, Shun-Chiao Chang, Stacey B. Gabriel, Casey Gates, Ellen Hanson, Andrew Kirby, Joshua M. Korn, Finny G. Kuruvilla, Steven McCarroll, Eric M. Morrow, Benjamin M. Neale, Shaun Purcell, Roksana Sasanfar, Carrie Sougnez, Christine Stevens, David Altshuler, James F. Gusella, Susan L. Santangelo, Pamela Sklar, Rudolph E. Tanzi, Richard Anney, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Catalina Betancur, Sven Bölte, Patrick Bolton, Jessica Brian, Susan E. Bryson, Joseph D. Buxbaum, Ines Cabrito, Guiqing Cai, Rita M. Cantor, Hilary Coon, Judith Conroy, Catarina Correia, Christina Corsello, Emily L. Crawford, Michael L. Cuccaro, Géraldine Dawson, Maretha Jonge, Bernie Devlin, Eftichia Duketis, Sean Ennis, Annette Estes, Penny Farrar, Éric Fombonne, Christine M. Freitag, Louise Gallagher, Daniel H. Geschwind, John R. Gilbert, Michael Gill, Christopher Gillberg, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Jonathan L. Haines, Joachim Hallmayer, Vanessa Hus, Sabine M. Klauck, Olena Korvatska, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L. Leventha, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Elena Maestrini, Tiago R. Magalhães, William J. Mahoney, Carine Mantoulan, Helen McConachie, Christopher J. McDougle, William M. McMahon, Christian R. Marshall, Judith Miller, Nancy J. Minshew, Anthony P. Monaco, Jeff Munson, John I. Nürnberger, Guiomar Oliveira, Alistair T. Pagnamenta, Katerina Papanikolaou, Jeremy Parr, Andrew D. Paterson
Publicat 2009Artigo
Eines de cerca:
Matèries relacionades
Autism
Biology
Genetics
Psychology
Medicine
Autism spectrum disorder
Developmental psychology
Gene
Psychiatry
Pediatrics
Genome
Phenotype
Genotype
Pregnancy
Single-nucleotide polymorphism
Copy-number variation
Heritability of autism
Birth weight
Genome-wide association study
Head circumference
Allele
Candidate gene
Chromosome
Clinical psychology
Genetic association
Genetic linkage
Internal medicine
Linkage (software)
Mathematics
SNP