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Analysis of financial barriers experienced by prospective genetic counseling students

Genetics in medicine, 2024-11, Vol.26 (11), p.101175, Article 101175

2024

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Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors

Journal of genetic counseling, 2013-06, Vol.22 (3), p.291-295

2013

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A Replication of the Autism Diagnostic Observation Schedule (ADOS) Revised Algorithms

Journal of the American Academy of Child and Adolescent Psychiatry, 2008-06, Vol.47 (6), p.642-651

2008

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Hereditary Cancer Clinics Improve Adherence to NCCN Germline Testing Guidelines for Pancreatic Cancer

Journal of the National Comprehensive Cancer Network, 2024-07, Vol.22 (5), p.299-305

2024

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Expanded Insights Into Mechanisms of Gene Expression and Disease Related Disruptions

Frontiers in molecular biosciences, 2018-11, Vol.5, p.101-101

2018

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Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader‐Willi syndrome: A multicenter study

Clinical genetics, 2021-07, Vol.100 (1), p.29-39

2021

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Nuclear and Mitochondrial Genome Defects in Autisms

Annals of the New York Academy of Sciences, 2009-01, Vol.1151 (1), p.102-132

2009

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Susceptibility to anthrax lethal toxin-induced rat death is controlled by a single chromosome 10 locus that includes rNlrp1

PLoS pathogens, 2010-05, Vol.6 (5), p.e1000906-e1000906

2010

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Mitochondrial and ion channel gene alterations in autism

Biochimica et biophysica acta, 2012-10, Vol.1817 (10), p.1796-1802

2012

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Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (1), p.309-314

2002

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Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome

Journal of clinical medicine, 2022-05, Vol.11 (9), p.2572

2022

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Language and other regression: Assessment and timing

Journal of autism and developmental disorders, 2003-12, Vol.33 (6), p.607-616

2003

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A Genome Survey Indicates a Possible Susceptibility Locus for Bipolar Disorder on Chromosome 22

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.585-590

2001

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A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R

BMC medical genetics, 2004-04, Vol.5 (1), p.10-10, Article 10

2004

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Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract

American journal of ophthalmology, 2006-04, Vol.141 (4), p.761-761.e4

2006

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Attention Deficit/Hyperactivity Disorder Children with a 7-Repeat Allele of the Dopamine Receptor D4 Gene Have Extreme Behavior but Normal Performance on Critical Neuropsychological Tests of Attention

Proceedings of the National Academy of Sciences - PNAS, 2000-04, Vol.97 (9), p.4754-4759

2000

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Gene Conversion Mutation in Crystallin, β-B2 ( CRYBB2 ) in a Chilean Family with Autosomal Dominant Cataract

Ophthalmology (Rochester, Minn.), 2007-03, Vol.114 (3), p.425-432

2007

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Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis

Genetics in medicine, 2014-04, Vol.16 (4), p.302-310

2014

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Ethnic disparities in the frequency of cancer reported in family histories

Journal of genetic counseling, 2020-06, Vol.29 (3), p.451-459

2020

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Adherence to NCCN screening guidelines for germline testing of patients with pancreatic cancer at a large academic medical center: A retrospective chart review

Journal of clinical oncology, 2022-10, Vol.40 (28_suppl), p.342-342

2022

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sequenced rat brain transcriptome – its use in identifying networks predisposing alcohol consumption

The FEBS journal, 2015-09, Vol.282 (18), p.3556-3578

2015

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Risk calculations: Still essential in the molecular age

American journal of medical genetics. Part A, 2004-09, Vol.129A (3), p.215-217

2004

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Molecular subtype and growth hormone effects on dysmorphology in Prader–Willi syndrome

American journal of medical genetics. Part A, 2020-01, Vol.182 (1), p.169-175

2020

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A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia

Journal of community genetics, 2019-07, Vol.10 (3), p.351-361

2019

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Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives

Journal of autoimmunity, 2008-09, Vol.31 (2), p.160-165

2008

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Analysis of financial barriers experienced by prospective genetic counseling students

Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors

A Replication of the Autism Diagnostic Observation Schedule (ADOS) Revised Algorithms

Hereditary Cancer Clinics Improve Adherence to NCCN Germline Testing Guidelines for Pancreatic Cancer

Expanded Insights Into Mechanisms of Gene Expression and Disease Related Disruptions

Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader‐Willi syndrome: A multicenter study

Nuclear and Mitochondrial Genome Defects in Autisms

Susceptibility to anthrax lethal toxin-induced rat death is controlled by a single chromosome 10 locus that includes rNlrp1

Mitochondrial and ion channel gene alterations in autism

Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus

Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome

Language and other regression: Assessment and timing

A Genome Survey Indicates a Possible Susceptibility Locus for Bipolar Disorder on Chromosome 22

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R

Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract

Attention Deficit/Hyperactivity Disorder Children with a 7-Repeat Allele of the Dopamine Receptor D4 Gene Have Extreme Behavior but Normal Performance on Critical Neuropsychological Tests of Attention

Gene Conversion Mutation in Crystallin, β-B2 ( CRYBB2 ) in a Chilean Family with Autosomal Dominant Cataract

Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis

Ethnic disparities in the frequency of cancer reported in family histories

Adherence to NCCN screening guidelines for germline testing of patients with pancreatic cancer at a large academic medical center: A retrospective chart review

sequenced rat brain transcriptome – its use in identifying networks predisposing alcohol consumption

Risk calculations: Still essential in the molecular age

Molecular subtype and growth hormone effects on dysmorphology in Prader–Willi syndrome

A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia

Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives

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