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MicroRNA miR-125a controls hematopoietic stem cell number

Proceedings of the National Academy of Sciences - PNAS, 2010-08, Vol.107 (32), p.14229-14234

2010

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Clinical exome sequencing for genetic identification of rare Mendelian disorders

JAMA : the journal of the American Medical Association, 2014-11, Vol.312 (18), p.1880

2014

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American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss

Genetics in medicine, 2014-04, Vol.16 (4), p.347-355

2014

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Corifollitropin Alfa Combined With Human Chorionic Gonadotropin in Adolescent Boys With Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2022-06, Vol.107 (7), p.2036-2046

2022

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Organizational Strategies Partially Account for Race-related Differences in List Recall Performance

Archives of clinical neuropsychology, 2019-02, Vol.34 (1), p.70-80

2019

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A Patient with Syncope

The New England journal of medicine, 2013-09, Vol.369 (10), p.966-972

2013

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Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins

Scientific reports, 2016-11, Vol.6 (1), p.37081-37081, Article 37081

2016

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A Patient with Syncope

The New England journal of medicine, 2013-08, Vol.369 (7), p.e9

2013

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Interactive medical case. A patient with syncope

The New England journal of medicine, 2013-08, Vol.369 (7), p.e9-e9

2013

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Pyrin Modulates the Intracellular Distribution of PSTPIP1

PloS one, 2009-07, Vol.4 (7), p.e6147-e6147

2009

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Sessional academic success : a distributed framework for academic support and development

Journal of university teaching & learning practice, 2013-01, Vol.10 (3), p.146-162

2013

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Retrovirally Marked CD34-Enriched Peripheral Blood and Bone Marrow Cells Contribute to Long-Term Engraftment After Autologous Transplantation

Blood, 1995-06, Vol.85 (11), p.3048-3057

1995

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Infant hearing loss and connexin testing in a diverse population

Genetics in medicine, 2008-07, Vol.10 (7), p.517-524

2008

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eP430: Genetics professionals’ perspectives on the reporting of Variants of Uncertain Significance (VUS): Should they always be reported?

Genetics in medicine, 2022-03, Vol.24 (3), p.S269-S269

2022

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Pyrin and ASC Co-Localize to Cellular Sites that Are Rich in Polymerizing Actin

Experimental biology and medicine (Maywood, N.J.), 2009-01, Vol.234 (1), p.40-52

2009

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Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder?

Genetics in medicine, 2017-12, Vol.19 (12), p.1380-1381

2017

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Collection Development and User Experience Symposia

Weave (Ann Arbor, Mich.), 2018-03, Vol.1 (8)

2018

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Clinical problem-solving. A patient with syncope

The New England journal of medicine, 2013-09, Vol.369 (10), p.966-972

2013

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Deaf Adults' Reasons for Genetic Testing Depend on Cultural Affiliation: Results From a Prospective, Longitudinal Genetic Counseling and Testing Study

Journal of deaf studies and deaf education, 2010-01, Vol.15 (3), p.209-227

2010

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Lack of Predictive Value of KIR-HLA Genotypes for Autologous Transplant Outcome for Multiple Myeloma

Blood, 2006-11, Vol.108 (11), p.3078-3078

2006

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Serum Free-Lite Chain (sFLC) Assay in Multiple Myeloma (MM): Clinical Correlates and Prognostic Implications in Newly Diagnosed MM Patients Treated with Total Therapy 2 or 3 (TT2/3)

Blood, 2005-11, Vol.106 (11), p.3490-3490

2005

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Genetic testing as part of the Early Hearing Detection and Intervention (EHDI) process

Genetics in medicine, 2004-11, Vol.6 (6), p.521-525

2004

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Retrospective Analysis of Fractionated High-Dose Melphalan (F-MEL) and Bortezomib-Thalidomide-Dexamethasone (VTD) with Autotransplant (AT) Support for Advanced and Refractory Multiple Myeloma (AR-MM)

Blood, 2006-11, Vol.108 (11), p.3102-3102

2006

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A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome

JIMD Reports - Volume 11, 2013, Vol.11, p.99-106

2013

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MicroRNA miR-125a controls hematopoietic stem cell number

Clinical exome sequencing for genetic identification of rare Mendelian disorders

American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss

Corifollitropin Alfa Combined With Human Chorionic Gonadotropin in Adolescent Boys With Hypogonadotropic Hypogonadism

Organizational Strategies Partially Account for Race-related Differences in List Recall Performance

A Patient with Syncope

Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins

A Patient with Syncope

Interactive medical case. A patient with syncope

Pyrin Modulates the Intracellular Distribution of PSTPIP1

Sessional academic success : a distributed framework for academic support and development

Retrovirally Marked CD34-Enriched Peripheral Blood and Bone Marrow Cells Contribute to Long-Term Engraftment After Autologous Transplantation

Infant hearing loss and connexin testing in a diverse population

eP430: Genetics professionals’ perspectives on the reporting of Variants of Uncertain Significance (VUS): Should they always be reported?

DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies

Pyrin and ASC Co-Localize to Cellular Sites that Are Rich in Polymerizing Actin

Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder?

Collection Development and User Experience Symposia

Clinical problem-solving. A patient with syncope

Deaf Adults' Reasons for Genetic Testing Depend on Cultural Affiliation: Results From a Prospective, Longitudinal Genetic Counseling and Testing Study

Lack of Predictive Value of KIR-HLA Genotypes for Autologous Transplant Outcome for Multiple Myeloma

Serum Free-Lite Chain (sFLC) Assay in Multiple Myeloma (MM): Clinical Correlates and Prognostic Implications in Newly Diagnosed MM Patients Treated with Total Therapy 2 or 3 (TT2/3)

Genetic testing as part of the Early Hearing Detection and Intervention (EHDI) process

Retrospective Analysis of Fractionated High-Dose Melphalan (F-MEL) and Bortezomib-Thalidomide-Dexamethasone (VTD) with Autotransplant (AT) Support for Advanced and Refractory Multiple Myeloma (AR-MM)

A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome

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