Lisa Osiecki

ORCID: 0000-0002-9408-8722
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About
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Research Areas
  • Obsessive-Compulsive Spectrum Disorders
  • Autism Spectrum Disorder Research
  • Williams Syndrome Research
  • Genetic Associations and Epidemiology
  • Eating Disorders and Behaviors
  • Genomic variations and chromosomal abnormalities
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Virology and Viral Diseases
  • Trypanosoma species research and implications
  • Child and Adolescent Psychosocial and Emotional Development
  • Plant Virus Research Studies
  • Schizophrenia research and treatment
  • Plant Reproductive Biology
  • Hereditary Neurological Disorders
  • Child Nutrition and Feeding Issues
  • Attention Deficit Hyperactivity Disorder
  • Urticaria and Related Conditions
  • Chromosomal and Genetic Variations

Harvard University
2012-2025

Massachusetts General Hospital
2015-2025

NeuroDevelopment Center
2021-2024

Harvard University Press
2023

Yale University
2021

Broad Institute
2014-2019

Stanley Foundation
2019

Center for Human Genetics
2010-2017

Brigham and Women's Hospital
2014-2017

VA Boston Healthcare System
2017

Tourette syndrome (TS) is characterized by high rates of psychiatric comorbidity; however, few studies have fully these comorbidities. Furthermore, most included relatively participants (<200), and none has examined the ages highest risk for each TS-associated comorbidity or their etiologic relationship to TS.To characterize lifetime prevalence, clinical associations, risk, etiology among individuals with TS.Cross-sectional structured diagnostic interviews conducted between April 1, 1992,...

10.1001/jamapsychiatry.2014.2650 article EN JAMA Psychiatry 2015-02-11
Lea K. Davis Dongmei Yu Clare L. Keenan Eric R. Gamazon Anuar Konkashbaev and 95 more Eske M. Derks Benjamin M. Neale Jian Yang Sang Lee Patrick Evans Cathy L. Barr Laura Bellodi Fortu Benarroch Gabriel Bedoya Berrío O. Joseph Bienvenu Michael H. Bloch Rianne M. Blom Ruth D. Bruun Cathy L. Budman Beatríz Camarena Desmond Campbell Carolina Cappi Julio César Cardona Silgado Daniëlle C. Cath Maria Cristina Cavallini Denise A. Chavira Sylvain Chouinard David V. Conti Edwin H. Cook Vladimir Coric Bernadette Cullen Dieter Deforce Richard Delorme Yves Dion Christopher K. Edlund Karin Egberts Peter Falkai Thomas Fernandez Patience Gallagher Helena Garrido Daniel Geller Simon Girard Hans J. Grabe Marco A. Grados Benjamin D. Greenberg Varda Gross‐Tsur Stephen A. Haddad Gary A. Heiman Sian Hemmings Ana Gabriela Hounie Cornelia Illmann Joseph Jankovic Michael A. Jenike James L. Kennedy Robert A. King Bárbara Kremeyer Roger Kurlan Nuria Lanzagorta Marion Leboyer James F. Leckman Leonhard Lennertz Chunyu Liu Christine Löchner Thomas L. Lowe Fabìo Macciardi James T. McCracken Lauren M. McGrath Sandra Catalina Mesa Restrepo Rainald Moessner Jubel Morgan Heike Müller Dennis L. Murphy Allan L. Naarden William Cornejo Ochoa Roel A. Ophoff Lisa Osiecki A.J. Pakstis Michele T. Pato Carlos N. Pato John Piacentini Christopher Pittenger Yehuda Pollak Scott L. Rauch Tobias Renner Victor I. Reus Margaret A. Richter Mark A. Riddle Mary M. Robertson Roxana Romero Maria Conceição do Rosário David Rosenberg Guy A. Rouleau Stephan Ruhrmann Andrés Ruiz‐Linares Aline S. Sampaio Jack Samuels Paul Sandor Brooke Sheppard Harvey S. Singer Jan Smit

The direct estimation of heritability from genome-wide common variant data as implemented in the program Genome-wide Complex Trait Analysis (GCTA) has provided a means to quantify attributable all interrogated variants. We have quantified variance liability disease explained by SNPs for two phenotypically-related neurobehavioral disorders, obsessive-compulsive disorder (OCD) and Tourette Syndrome (TS), using GCTA. Our analysis yielded point estimate 0.58 (se = 0.09, p 5.64e-12) TS, 0.37...

10.1371/journal.pgen.1003864 article EN cc-by PLoS Genetics 2013-10-24
Jeremiah M. Scharf Dongmei Yu Carol A. Mathews Benjamin M. Neale S. Evelyn Stewart and 93 more Jesen Fagerness Patrick Evans Eric R. Gamazon Christopher K. Edlund Susan K. Service А. А. Тихомиров Lisa Osiecki Caroline Illmann Anna Pluzhnikov Anuar Konkashbaev Lea K. Davis Buhm Han Jacquelyn Crane Priya Moorjani Andrew Crenshaw Melissa Parkin Victor I. Reus Trevor Lowe Martha Rangel‐Lugo Sylvain Chouinard Yves Dion Simon Girard Daniëlle C. Cath Jan Smit Robert A. King Thomas Fernandez James F. Leckman Kenneth K. Kídd J.R. Kidd A.J. Pakstis Matthew W. State Luis Diego Herrera Roberto Romero Eduardo Fournier Paul Sandor Cathy L. Barr N. Phan Varda Gross‐Tsur Fortu Benarroch Yehuda Pollak Cathy L. Budman Ruth D. Bruun Gerald Erenberg Allan L. Naarden Paul C. Lee Noel S. Weiss Bárbara Kremeyer Gabriel Bedoya Berrío Desmond Campbell Julio César Cardona Silgado William Cornejo Ochoa Sandra Catalina Mesa Restrepo Hans‐Helge Müller Ana V. Valencia Duarte Gholson J. Lyon M. Leppert J L Morgan Robert B. Weiss Marco A. Grados Kari Anderson Shekar Davarya Harvey S. Singer John T. Walkup Joseph Jankovic Jay A. Tischfield Gary A. Heiman Donald L. Gilbert Pieter J. Hoekstra Mary M. Robertson Roger Kurlan Chunyu Liu J. Raphael Gibbs Andrew B. Singleton John Hardy E Strengman Roel A. Ophoff Michael Wagner R. Moessner Daniel B. Mirel Daniëlle Posthuma C. Sabatti Eleazar Eskin D V Conti James A. Knowles Andrés Ruiz‐Linares Guy A. Rouleau Shaun Purcell Peter Heutink Ben A. Oostra William M. McMahon Nelson B. Freimer Nancy J. Cox David L. Pauls

10.1038/mp.2012.69 article EN Molecular Psychiatry 2012-08-14
Dongmei Yu Carol A. Mathews Jeremiah M. Scharf Benjamin M. Neale Lea K. Davis and 95 more Eric R. Gamazon Eske M. Derks Patrick Evans Christopher K. Edlund Jacquelyn Crane Jesen Fagerness Lisa Osiecki Patience Gallagher Gloria F. Gerber Stephen A. Haddad Cornelia Illmann Lauren M. McGrath C Mayerfeld Sampath Arepalli Cristina Barlassina Cathy L. Barr Laura Bellodi Fortu Benarroch Gabriel Bedoya Berrío O. Joseph Bienvenu Donald W. Black Michael H. Bloch Helena Brentani Ruth D. Bruun Cathy L. Budman Beatríz Camarena Desmond Campbell Carolina Cappi Julio César Cardona Silgado Maria Cristina Cavallini Denise A. Chavira Sylvain Chouinard Edwin H. Cook Mark Cookson Vladimir Coric Bernadette Cullen Daniele Cusi Richard Delorme Damiaan Denys Yves Dion Valsamma Eapen Karin Egberts Peter Falkai Thomas Fernandez Eduardo Fournier Helena Garrido Daniel Geller Donald L. Gilbert Simon Girard Hans J. Grabe Marco A. Grados Benjamin D. Greenberg Varda Gross‐Tsur Edna Grünblatt John Hardy Gary A. Heiman Sian Hemmings Luis Diego Herrera Dianne M. Hezel Pieter J. Hoekstra Joseph Jankovic James L. Kennedy Robert A. King Anuar Konkashbaev Bárbara Kremeyer Roger Kurlan Nuria Lanzagorta Marion Leboyer James F. Leckman Leonhard Lennertz Chunyu Liu Christine Löchner Thomas L. Lowe Sara Lupoli Fabìo Macciardi Wolfgang Maier Paolo Manunta Maurizio Marconi James T. McCracken Sandra Catalina Mesa Restrepo Rainald Moessner Priya Moorjani Jubel Morgan Heike Müller Dennis L. Murphy Allan L. Naarden Erika L. Nurmi William Cornejo Ochoa Roel A. Ophoff A.J. Pakstis Michele T. Pato Carlos N. Pato John Piacentini Christopher Pittenger Yehuda Pollak

Objective: Obsessive-compulsive disorder (OCD) and Tourette's syndrome are highly heritable neurodevelopmental disorders that thought to share genetic risk factors. However, the identification of definitive susceptibility genes for these etiologically complex remains elusive. The authors report a combined genome-wide association study (GWAS) OCD. Method: conducted GWAS in 2,723 cases (1,310 with OCD, 834 syndrome, 579 OCD plus syndrome/chronic tics), 5,667 ancestry-matched controls, 290...

10.1176/appi.ajp.2014.13101306 article EN American Journal of Psychiatry 2014-08-26
Lauren M. McGrath Dongmei Yu Christian Marshall Lea K. Davis Bhooma Thiruvahindrapuram and 95 more Bingbin Li Carolina Cappi Gloria F. Gerber Aaron B. Wolf Frederick A. Schroeder Lisa Osiecki Colm O’Dushlaine Andrew Kirby Cornelia Illmann Stephen A. Haddad Patience Gallagher Jesen Fagerness Cathy L. Barr Laura Bellodi Fortu Benarroch O. Joseph Bienvenu Donald W. Black Michael H. Bloch Ruth D. Bruun Cathy L. Budman Beatríz Camarena Daniëlle C. Cath Maria Cristina Cavallini Sylvain Chouinard Vladimir Coric Bernadette Cullen Richard Delorme Damiaan Denys Eske M. Derks Yves Dion Maria Conceição do Rosário Valsamma Eapen Patrick Evans Peter Falkai Thomas Fernandez Helena Garrido Daniel Geller Hans J. Grabe Marco A. Grados Benjamin D. Greenberg Varda Gross‐Tsur Edna Grünblatt Gary A. Heiman Sian Hemmings Luis Diego Herrera Ana Gabriela Hounie Joseph Jankovic James L. Kennedy Robert A. King Roger Kurlan Nuria Lanzagorta Marion Leboyer James F. Leckman Leonhard Lennertz Christine Löchner Thomas L. Lowe Gholson J. Lyon Fabìo Macciardi Wolfgang Maier James T. McCracken William McMahon Dennis L. Murphy Allan L. Naarden Benjamin M. Neale Erika L. Nurmi A.J. Pakstis Michele T. Pato Carlos N. Pato John Piacentini Christopher Pittenger Yehuda Pollak Victor I. Reus Margaret A. Richter Mark A. Riddle Mary M. Robertson David Rosenberg Guy A. Rouleau Stephan Ruhrmann Aline S. Sampaio Jack Samuels Paul Sandor Brooke Sheppard Harvey S. Singer Jan Smit Dan J. Stein Jay A. Tischfield Homero Vallada Jeremy Veenstra‐VanderWeele Susanne Walitza Ying Wang Jens R. Wendland Yin Yao Shugart Eurípedes C. Miguel Humberto Nicolini Ben A. Oostra

10.1016/j.jaac.2014.04.022 article EN Journal of the American Academy of Child & Adolescent Psychiatry 2014-06-24
Nora I. Strom Zachary F. Gerring Marco Galimberti Dongmei Yu Matthew Halvorsen and 95 more Abdel Abdellaoui Cristina Rodriguez‐Fontenla Julia Sealock Tim B. Bigdeli Jonathan R. I. Coleman Behrang Mahjani Jackson G. Thorp Katharina Bey Christie L. Burton Jurjen J. Luykx Gwyneth Zai Silvia Alemany Christine André Kathleen D. Askland Nerisa Banaj Cristina Barlassina Judith Becker Nissen O. Joseph Bienvenu Donald W. Black Michael H. Bloch Julia Boberg Sigrid Børte Rosa Bosch Michael S. Breen Brian P. Brennan Helena Brentani Joseph D. Buxbaum Jonas Bybjerg‐Grauholm Enda M. Byrne Judit Cabana‐Domínguez Beatríz Camarena Adrian Camarena Carolina Cappi Ángel Carracedo Miguel Casas Maria Cristina Cavallini Valentina Ciullo Edwin H. Cook Jesse M. Crosby Bernadette Cullen Elles de Schipper Richard Delorme Srdjan Djurovic Jason A. Elias Xavier Estivill Martha J. Falkenstein Bengt T. Fundín Lauryn E. Garner Chris German Christina Gironda Fernando S. Goes Marco A. Grados Jakob Grove Wei Guo Jan Haavik Kristen Hagen Kelly Harrington Alexandra Havdahl Kira Höffler Ana Gabriela Hounie Donald Hucks Christina M. Hultman Magdalena Janecka Eric Jenike Elinor K. Karlsson Kara N. Kelley Julia Klawohn Janice Krasnow Kristi Krebs Christoph Lange Nuria Lanzagorta Daniel F. Levey Kerstin Lindblad‐Toh Fabìo Macciardi Brion S. Maher Brittany M. Mathes Evonne McArthur Nathaniel W. McGregor Nicole McLaughlin Sandra Meier Eurípedes C. Miguel Maureen Mulhern Paul S. Nestadt Erika L. Nurmi Kevin S. O’Connell Lisa Osiecki Olga Therese Ousdal Teemu Palviainen Nancy L. Pedersen Fabrizio Piras Federica Piras Sriramya Potluri Raquel Rabionet Alfredo Ramı́rez Scott L. Rauch

Obsessive-compulsive disorder (OCD) affects ~1% of the population and exhibits a high SNP-heritability, yet previous genome-wide association studies (GWAS) have provided limited information on genetic etiology underlying biological mechanisms disorder. We conducted GWAS meta-analysis combining 53,660 OCD cases 2,044,417 controls from 28 European-ancestry cohorts revealing 30 independent significant SNPs SNP-based heritability 6.7%. Separate for clinical, biobank, comorbid, self-report...

10.1101/2024.03.13.24304161 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2024-03-13
Fotis Tsetsos Dongmei Yu Jae Hoon Sul Alden Y. Huang Cornelia Illmann and 95 more Lisa Osiecki Sabrina M. Darrow Matthew E. Hirschtritt Erica Greenberg Kirsten Müller‐Vahl Manfred Stuhrmann Yves Dion Guy A. Rouleau H.N. Aschauer M. Stamenković Monika Schlögelhofer Paul Sandor Cathy L. Barr Marco A. Grados Harvey S. Singer Markus M. Nöthen Johannes Hebebrand Anke Hinney Robert A. King Thomas Fernandez Csaba Barta Zsanett Tárnok Péter Nagy Christel Depienne Yulia Worbe Andreas Hartmann Cathy L. Budman Renata Rizzo Gholson J. Lyon William M. McMahon James R. Batterson Daniëlle C. Cath Irene A. Malaty Michael S. Okun Cheston M. Berlin Douglas W. Woods Paul C. Lee Joseph Jankovic Mary M. Robertson Donald L. Gilbert Lawrence W. Brown Barbara J. Coffey Andrea Dietrich Pieter J. Hoekstra Samuel Kuperman Samuel H. Zinner Michael Wagner James A. Knowles A. Jeremy Willsey Jay A. Tischfield Gary A. Heiman Nancy J. Cox Nelson B. Freimer Benjamin M. Neale Lea K. Davis Giovanni Coppola Carol A. Mathews Jeremiah M. Scharf Peristera Paschou Cathy L. Barr James R. Batterson Cheston M. Berlin Cathy L. Budman Daniëlle C. Cath Giovanni Coppola Nancy J. Cox Sabrina M. Darrow Lea K. Davis Yves Dion Nelson B. Freimer Marco A. Grados Erica Greenberg Matthew E. Hirschtritt Alden Y. Huang Cornelia Illmann Robert A. King Roger Kurlan James F. Leckman Gholson J. Lyon Irene A. Malaty Carol A. Mathews William M. McMahon Benjamin M. Neale Michael S. Okun Lisa Osiecki Mary M. Robertson Guy A. Rouleau Paul Sandor Jeremiah M. Scharf Harvey S. Singer Jan Smit Jae Hoon Sul Dongmei Yu Harald Aschauer Harald Aschauer Csaba Barta

Abstract Tourette syndrome (TS) is a neuropsychiatric disorder of complex genetic architecture involving multiple interacting genes. Here, we sought to elucidate the pathways that underlie neurobiology through genome-wide analysis. We analyzed genotypic data 3581 individuals with TS and 7682 ancestry-matched controls investigated associations sets genes are expressed in particular cell types operate specific neuronal glial functions. employed self-contained, set-based association method...

10.1038/s41398-020-01082-z article EN cc-by Translational Psychiatry 2021-01-18

Abstract Tourette syndrome (TS) is a childhood‐onset neuropsychiatric disorder that familial and highly heritable. Although genetic influences are thought to play significant role in the development of TS, no definite TS susceptibility genes have been identified date. believed be genetically related both obsessive‐compulsive (OCD) grooming disorders (GD) such as trichotillomania (TTM). SAP90/PSD95‐associated protein 3 ( SAPAP3/DLGAP3 ) post‐synaptic scaffolding expressed glutamatergic...

10.1002/ajmg.b.31134 article EN American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010-11-02

Phenotypic heterogeneity in Tourette syndrome is partly due to complex genetic relationships among syndrome, obsessive-compulsive disorder (OCD), and attention deficit hyperactivity (ADHD). Identifying symptom-based endophenotypes across diagnoses may aid gene-finding efforts.Assessments for OCD, ADHD symptoms were conducted a discovery sample of 3,494 individuals recruited studies. Symptom-level factor latent class analyses families replicated an independent 882 individuals. Classes...

10.1176/appi.ajp.2016.16020240 article EN American Journal of Psychiatry 2016-11-04

Background The unique phenotypic and genetic aspects of obsessive-compulsive (OCD) attention-deficit/hyperactivity disorder (ADHD) among individuals with Tourette syndrome (TS) are not well characterized. Here, we examine symptom patterns heritability OCD ADHD in TS families. Method were examined patients their family members ( N = 3494) using exploratory factor analyses (EFA) for symptoms separately, followed by latent class (LCA) the resulting sum scores jointly; clinical relevance factors...

10.1017/s0033291717001672 article EN Psychological Medicine 2017-06-27

Persistent motor or vocal tic disorder (PMVT) has been hypothesized to be a forme fruste of Tourette syndrome (TS). Although the primary diagnostic criterion for PMVT (presence tics, but not both) is clear, less known about its clinical presentation.The goals this study were compare prevalence and number comorbid psychiatric disorders, severity, age at onset, family history TS PMVT.We analyzed data from two independent cohorts using generalized linear equations confirmed our findings...

10.1002/mds.28593 article EN Movement Disorders 2021-05-04
Nora I. Strom Dongmei Yu Zachary F. Gerring Matthew Halvorsen Abdel Abdellaoui and 95 more Cristina Rodriguez‐Fontenla Julia Sealock Tim B. Bigdeli Jonathan R. I. Coleman Behrang Mahjani Jackson G. Thorp Katharina Bey Christie L. Burton Jurjen J. Luykx Gwyneth Zai Kathleen D. Askland Cristina Barlassina Judith Becker Nissen Laura Bellodi O. Joseph Bienvenu Donald W. Black Michael H. Bloch Julia Boberg Rosa Bosch Michael S. Breen Brian P. Brennan Helena Brentani Joseph D. Buxbaum Jonas Bybjerg‐Grauholm Enda M. Byrne Beatríz Camarena Adrian Camarena Carolina Cappi Ángel Carracedo Miguel Casas Maria Cristina Cavallini Valentina Ciullo Edwin H. Cook Vladimir Coric Bernadette Cullen Elles de Schipper Bernie Devlin Srdjan Djurovic Jason A. Elias Lauren Erdman Xavier Estivil Martha J. Falkenstein Bengt T. Fundín Maiken E. Gabrielsen Fernando S. Goes Marco A. Grados Jakob Grove Wei Guo Jan Haavik Kristen Hagen Alexandra Havdahl Ana Gabriela Hounie Donald Hucks Christina M. Hultman Magdalena Janecka Michael A. Jenike Elinor K. Karlsson Julia Klawohn Lambertus Klei Janice Krasnow Kristi Krebs Jason W. Krompinger Nuria Lanzagorta Fabìo Macciardi Brion S. Maher Evonne McArthur Nathaniel W. McGregor Nicole McLaughlin Sandra Meier Eurípedes C. Miguel Maureen Mulhern Paul S. Nestadt Erika L. Nurmi Kevin S. O’Connell Lisa Osiecki Teemu Palviainen Fabrizio Piras Federica Piras Ann E. Pulver Raquel Rabionet Alfredo Ramı́rez Scott L. Rauch Abraham Reichenberg Jennifer Reichert Mark A. Riddle Stephan Ripke Aline S. Sampaio Miriam A. Schiele Laura Sloofman Jan Smit Janet L. Sobell María Soler Artigas Laurent F. Thomas Homero Vallada Jeremy Veenstra‐VanderWeele

Obsessive-compulsive disorder (OCD) is a heritable disorder, but no definitive, replicated OCD susceptibility loci have yet been identified by any genome-wide association study (GWAS). Here, we report results from GWAS in the largest case-control sample (N = 14,140 cases and N 562,117 controls) to date. We explored genetic architecture of OCD, including its relationships other psychiatric non-psychiatric phenotypes. In analysis, one SNP associated with at significant level. Subsequent...

10.1101/2021.10.13.21261078 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2021-10-23

Tourette Syndrome (TS) and Persistent Motor or Vocal Tic Disorders (PMVT) are more prevalent in males (vs. females). Females with TS may have a delay diagnosis, complex tic features males). With respect to comorbidities, obsessive-compulsive disorder (OCD) is females; attention-deficit hyperactivity (ADHD) males. Less known about sex differences PMVT. This study analyzes outcomes among individuals PMVT the Association of America International Consortium for Genetics dataset (TAAICG).

10.1101/2024.01.07.24300816 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2024-01-09

To analyze sex differences in outcomes Tourette syndrome (TS) and Persistent Motor or Vocal tic disorders (PMVT) the Association of America International Consortium for Genetics (TAAICG) dataset. The relationship between clinical measures was explored 2,403 participants (N = 2,109 with TS; N 294 PMVT) from TAAICG dataset using generalized estimating equation regression models, adjusted age family relationships. Female (vs male) TS (25.5% sample) had 0.46 times lower odds being formally...

10.1212/wnl.0000000000210249 article EN Neurology 2025-01-15

Background The effects of the menstrual cycle on neuropsychiatric and physical symptoms have been examined in multiple psychiatric illnesses, but research Tourette syndrome (TS) menstruation is limited inconclusive. One study published 1992 reported that 34% female respondents experienced tic fluctuations with their cycles; however, a subsequent 2001 found no significant relationship between cycle-related hormonal changes across participants. There has further exploration this topic...

10.3389/fneur.2025.1500766 article EN cc-by Frontiers in Neurology 2025-02-11
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