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One Year into the COVID-19 Pandemic: an Update on Medical Student Experiences and Well-being

Journal of general internal medicine : JGIM, 2023-01, Vol.38 (1), p.273-276

2023

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A genome-wide search for loci contributing to smoking and alcoholism

Genetic epidemiology, 1999, Vol.17 (S1), p.S55-S60

1999

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Compulsive Behavior in Generalized Anxiety Disorder and Obsessive-Compulsive Disorder

The journal of nervous and mental disease, 1999-11, Vol.187 (11), p.697-699

1999

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Segregation analysis of diastolic blood pressure in a large pedigree

Genetic epidemiology, 1993, Vol.10 (6), p.659-664

Weissbecker, Karen A.

1993

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Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program

The New England journal of medicine, 1985-07, Vol.313 (1), p.16

1985

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Biotinidase deficiency: Initial clinical features and rapid diagnosis

Annals of neurology, 1985-11, Vol.18 (5), p.614-617

1985

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Neonatal screening for biotinidase deficiency: Results of a 1-year pilot study

The Journal of pediatrics, 1986, Vol.108 (1), p.40-46

1986

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Sudden death associated with biotinidase deficiency

Pediatrics (Evanston), 1987-03, Vol.79 (3), p.482

1987

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875 BIOTINIDASE DEFICIENCY DETECTED BY A STATEWIDE NEONATAL SCREENING PROGRAM

Pediatric research, 1985-04, Vol.19 (4), p.256-256A

1985

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Statistical approaches for the detection of heterozygotes for biotinidase deficiency

American journal of medical genetics, 1991-06, Vol.39 (4), p.385-390

1991

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Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: The usefulness of multiple study designs

American journal of medical genetics, 1993-08, Vol.47 (2), p.231-240

1993

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Tracking Medical Professionalism Across the Educational Continuum

Medical science educator, 2016-12, Vol.26 (4), p.733-736

2016

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Association study between the dopamine receptor D4 gene and obsessive-compulsive disorder

European neuropsychopharmacology, 2007-05, Vol.17 (6), p.406-409

2007

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Association study between the dopamine receptor D 4 gene and obsessive-compulsive disorder

European neuropsychopharmacology, 2007-05, Vol.17 (6), p.406-409

2007

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A DNA repeat, NBL2, is hypermethylated in some cancers but hypomethylated in others

Cancer biology & therapy, 2005-04, Vol.4 (4), p.446-454

2005

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Association study between the dopamine receptor D(4) gene and obsessive-compulsive disorder

European neuropsychopharmacology, 2007-05, Vol.17 (6-7), p.406-409

2007

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Imatinib (ST1571) provides only limited selectivity for CML cells and treatment might be complicated by silent BCR-ABL genes

Cancer biology & therapy, 2003-01, Vol.2 (1), p.103-108

2003

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Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome

Clinical dysmorphology, 2003-07, Vol.12 (3), p.161-165

2003

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Progress in Mapping Human Epilepsy Genes

Epilepsia (Copenhagen), 1994-01, Vol.35 (s1), p.S29-S40

1994

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Imatinib (STI571) Provides Only Limited Selectivity for CML Cells and Treatment Might Be Complicated by Silent BCR-ABL Genes

Cancer biology & therapy, 2003-01, Vol.2 (1), p.104-109

2003

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Imatinib (STI571) Provides Only Limited Selectivity for CML Cells and Treatment Might Be Complicated by Silent BCR-ABL Genes

Cancer biology & therapy, 2003-01, Vol.2 (1), p.102-107

2003

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Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome

Clinical dysmorphology, 2003-07, Vol.12 (3), p.161-165

2003

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Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis

Human heredity, 2000-03, Vol.50 (2), p.126-132

2000

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Gene Mapping in the Idiopathic Generalized Epilepsies: Juvenile Myoclonic Epilepsy, Childhood Absence Epilepsy, Epilepsy with Grand Mai Seizures, and Early Childhood Myoclonic Epilepsy

Epilepsia (Copenhagen), 1990-09, Vol.31 (s3), p.S19-S29

1990

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One Year into the COVID-19 Pandemic: an Update on Medical Student Experiences and Well-being

A genome-wide search for loci contributing to smoking and alcoholism

Compulsive Behavior in Generalized Anxiety Disorder and Obsessive-Compulsive Disorder

Segregation analysis of diastolic blood pressure in a large pedigree

Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program

Biotinidase deficiency: Initial clinical features and rapid diagnosis

Neonatal screening for biotinidase deficiency: Results of a 1-year pilot study

Sudden death associated with biotinidase deficiency

875 BIOTINIDASE DEFICIENCY DETECTED BY A STATEWIDE NEONATAL SCREENING PROGRAM

Statistical approaches for the detection of heterozygotes for biotinidase deficiency

Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: The usefulness of multiple study designs

Tracking Medical Professionalism Across the Educational Continuum

Association study between the dopamine receptor D4 gene and obsessive-compulsive disorder

Association study between the dopamine receptor D 4 gene and obsessive-compulsive disorder

A DNA repeat, NBL2, is hypermethylated in some cancers but hypomethylated in others

Association study between the dopamine receptor D(4) gene and obsessive-compulsive disorder

Imatinib (ST1571) provides only limited selectivity for CML cells and treatment might be complicated by silent BCR-ABL genes

Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome

Progress in Mapping Human Epilepsy Genes

Imatinib (STI571) Provides Only Limited Selectivity for CML Cells and Treatment Might Be Complicated by Silent BCR-ABL Genes

Imatinib (STI571) Provides Only Limited Selectivity for CML Cells and Treatment Might Be Complicated by Silent BCR-ABL Genes

Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome

Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis

Gene Mapping in the Idiopathic Generalized Epilepsies: Juvenile Myoclonic Epilepsy, Childhood Absence Epilepsy, Epilepsy with Grand Mai Seizures, and Early Childhood Myoclonic Epilepsy

Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic features

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