FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Lauren Weiss

Research Profile

Physiology

Disorders

Genes & Molecular Sequences

Chemicals & Drugs

Phenomena

Founder Effect

Concepts & Ideas

Co-author Network

Publications

TOP 3
Lauren A Weiss
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Lauren A Weiss; Dan E Arking; Mark J Daly; Aravinda Chakravarti
A genome-wide linkage and association scan reveals novel loci for autism.
Jeanette J McCarthy; Aleefia Somji; Lauren A Weiss; Brian Steffy; Raquel Vega; Elizabeth Barrett-Connor; Gregory A Talavera; Richard Glynne
Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Lauren Weiss (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2009: Lauren A Weiss
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Expert review of molecular diagnostics 2009;9(8):795-803.
2009: Lauren A Weiss; Dan E Arking; Mark J Daly; Aravinda Chakravarti
A genome-wide linkage and association scan reveals novel loci for autism.
Nature 2009;461(7265):802-8.
2009: Jeanette J McCarthy; Aleefia Somji; Lauren A Weiss; Brian Steffy; Raquel Vega; Elizabeth Barrett-Connor; Gregory A Talavera; Richard Glynne
Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction.
The Journal of clinical endocrinology and metabolism 2009;94(5):1789-96.
2009: D T Miller; Y Shen; Lauren A Weiss; J Korn; I Anselm; C Bridgemohan; G F Cox; H Dickinson; J Gentile; D J Harris; V Hegde; R Hundley; O Khwaja; S Kothare; C Luedke; R Nasir; A Poduri; K Prasad; P Raffalli; A Reinhard; S E Smith; M M Sobeih; J S Soul; J Stoler; M Takeoka; W-H Tan; J Thakuria; R Wolff; R Yusupov; James Gusella; Mark J Daly; B-L Wu
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
Journal of medical genetics 2009;46(4):242-8.
2009: Carolina Blaya; Priya Moorjani; Giovanni Salum; Leonardo Gonçalves; Lauren A Weiss; Sandra Leistner-Segal; Gisele G Manfro; Jordan W Smoller
Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance.
Neuroscience letters 2009;452(1):84-6.
2009: Lauren A Weiss
New insights into genomic variation in health and disease.
Genome medicine 2009;1(4):41.
2008: Lauren A Weiss; Yiping Shen; Joshua M Korn; Dan E Arking; David T Miller; Ragnheidur Fossdal; Evald Saemundsen; Hreinn Stefansson; Manuel A R Ferreira; Todd Green; Orah S Platt; Douglas M Ruderfer; Christopher Walsh; David Altshuler; Aravinda Chakravarti; Rudolph E Tanzi; Kari Stefansson; Susan L Santangelo; James Gusella; Pamela Sklar; Bai-Lin Wu; Mark J Daly
Association between microdeletion and microduplication at 16p11.2 and autism.
The New England journal of medicine 2008;358(7):667-75.
2008: Hyung-Goo Kim; Shotaro Kishikawa; Anne W Higgins; Ihn Sik Seong; Diana J Donovan; Yiping Shen; Eric Lally; Lauren A Weiss; Juliane Najm; Kerstin Kutsche; Maria Descartes; Lynn Holt; Stephen Braddock; Robin Troxell; Lee Kaplan; Fred Volkmar; Ami Klin; Katherine Tsatsanis; David J Harris; Ilse Noens; David L Pauls; Mark J Daly; Marcy E MacDonald; Cynthia C Morton; Bradley J Quade; James Gusella
Disruption of neurexin 1 associated with autism spectrum disorder.
American journal of human genetics 2008;82(1):199-207.
2008: Sarah Cross; Soo-Jeong Kim; Lauren A Weiss; Ryan J Delahanty; James S Sutcliffe; Bennett L Leventhal; Edwin H Cook; Jeremy Veenstra-VanderWeele
Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2008;33(2):353-60.
2007: Emma E Thompson; Lin Pan; Irina Ostrovnaya; Lauren A Weiss; James E Gern; Robert F Lemanske; Dan L Nicolae; Carole Ober
Integrin beta 3 genotype influences asthma and allergy phenotypes in the first 6 years of life.
The Journal of allergy and clinical immunology 2007;119(6):1423-9.
2007: Lauren A Weiss; Shaun Purcell; Skye Waggoner; Kate Lawrence; David Spektor; Mark J Daly; Pamela Sklar; David Skuse
Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.
Human molecular genetics 2007;16(1):107-13.
2006: Lauren A Weiss; Gülüm Kosova; Ryan J Delahanty; Lan Jiang; Edwin H Cook; Carole Ober; James S Sutcliffe
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.
European journal of human genetics : EJHG 2006;14(8):923-31.
2006: Lauren A Weiss; Carole Ober; Edwin H Cook
ITGB3 shows genetic and expression interaction with SLC6A4.
Human genetics 2006;120(1):93-100.
2006: Lauren A Weiss; Lin Pan; Mark Abney; Carole Ober
The sex-specific genetic architecture of quantitative traits in humans.
Nature genetics 2006;38(2):218-22.
2005: Lianne M Kurina; Lauren A Weiss; Steven W Graves; Rodney Parry; Gordon H Williams; Mark Abney; Carole Ober
Sex differences in the genetic basis of morning serum cortisol levels: genome-wide screen identifies two novel loci specific to women.
The Journal of clinical endocrinology and metabolism 2005;90(8):4747-52.
2005: Lauren A Weiss; Lucille A Lester; James E Gern; Raoul L Wolf; Rodney Parry; Robert F Lemanske; Julian Solway; Carole Ober
Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations.
American journal of respiratory and critical care medicine 2005;172(1):67-73.
2005: Lauren A Weiss; Mark Abney; Rodney Parry; Angelo M Scanu; Edwin H Cook; Carole Ober
Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample.
Human genetics 2005;117(1):81-7.
2005: Lauren A Weiss; Mark Abney; Edwin H Cook; Carole Ober
Sex-specific genetic architecture of whole blood serotonin levels.
American journal of human genetics 2005;76(1):33-41.
2004: Lauren A Weiss; Jeremy Veenstra-VanderWeele; Dina L Newman; Soo-Jeong Kim; Harvey Dytch; Mary Sara McPeek; Suzanne Cheng; Carole Ober; Edwin H Cook; Mark Abney
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin.
European journal of human genetics : EJHG 2004;12(11):949-54.
2003: Lauren A Weiss; Andrew Escayg; Jennifer A Kearney; M Trudeau; Bryan T MacDonald; M Mori; J Reichert; Joseph Buxbaum; Miriam H Meisler
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Molecular psychiatry 2003;8(2):186-94.