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Humans Use Directed and Random Exploration to Solve the Explore-Exploit Dilemma

Journal of experimental psychology. General, 2014-12, Vol.143 (6), p.2074-2081

2014

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Bayesian Online Learning of the Hazard Rate in Change-Point Problems

Neural computation, 2010-09, Vol.22 (9), p.2452-2476

2010

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Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2007-01, Vol.92 (1), p.137-142

2007

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Proteomic Study of Low-Temperature Responses in Strawberry Cultivars (Fragaria × ananassa) That Differ in Cold Tolerance

Plant physiology (Bethesda), 2012-08, Vol.159 (4), p.1787-1805

2012

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Parallel Hopfield Networks

Neural computation, 2009-03, Vol.21 (3), p.831-850

Wilson, Robert C.

2009

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Viral suppressor proteins show varying abilities and effectiveness to suppress transgene-induced post-transcriptional gene silencing of endogenous Chalcone synthase in transgenic Arabidopsis

Plant cell reports, 2008-05, Vol.27 (5), p.911-921

2008

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Two Novel Mutations Found in a Patient with 17α-Hydroxylase Enzyme Deficiency

The journal of clinical endocrinology and metabolism, 2006-10, Vol.91 (10), p.4179-4182

2006

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Apparent mineralocorticoid excess

Trends in Endocrinology & Metabolism, 2001-04, Vol.12 (3), p.104-111

2001

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In Vitro Expression Studies of a Novel Mutation Δ299 in a Patient Affected with Apparent Mineralocorticoid Excess

The journal of clinical endocrinology and metabolism, 2004-05, Vol.89 (5), p.2024-2027

2004

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Prenatal Diagnosis and Treatment of 11β-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Resulting in Normal Female Genitalia

The journal of clinical endocrinology and metabolism, 1999-09, Vol.84 (9), p.3129-3134

1999

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Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia

Pediatric research, 1999-11, Vol.46 (5), p.510-513

1999

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Glucocorticoid resistance caused by reduced expression of the glucocorticoid receptor in cells from human vascular lesions

Arteriosclerosis, thrombosis, and vascular biology, 1999-05, Vol.19 (5), p.1180

1999

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Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies

The journal of clinical endocrinology and metabolism, 2001-12, Vol.86 (12), p.5651-5657

2001

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Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess

The journal of clinical endocrinology and metabolism, 1998-07, Vol.83 (7), p.2244-2254

1998

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Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1995-07, Vol.80 (7), p.2014-2020

1995

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Commentary: The Education of a Faculty Developer

Journal of educational psychology, 1990-06, Vol.82 (2), p.272-274

Wilson, Robert C

1990

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Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene

The journal of clinical endocrinology and metabolism, 1995-05, Vol.80 (5), p.1635-1640

1995

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Several homozygous mutations in the gene for 11β-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3145-3150

1995

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Monogenic low renin hypertension : Endocrine hypertension

Trends in endocrinology and metabolism, 2005, Vol.16 (3), p.92-97

2005

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Distribution and abundance of marine bird and pinniped populations within Port Foster, Deception Island, Antarctica: Erupt: Ecosystem Studies at Deception Island, Antarctica

Deep-sea research. Part II, Topical studies in oceanography, 2003, Vol.50 (10-11), p.1873-1888

2003

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Profile of the pediatric endocrine clinic at New York-presbyterian hospital, New york weill cornell center

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4444-4449

1999

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Characterization of PRP1 and PRP2 from Medicago truncatula

Plant physiology (Bethesda), 1994-05, Vol.105 (1), p.445-446

1994

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Autonomous Splicing and Complementation of in Vivo-Assembled Spliceosomes

The Journal of cell biology, 1989-03, Vol.108 (3), p.765-777

1989

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A nodulin cDNA with homology to protochlorophyllide reductase

Plant physiology (Bethesda), 1994-01, Vol.104 (1), p.289-290

1994

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Complementation of in vitro-assembled spliceosomes

Journal of molecular biology, 1989-10, Vol.209 (3), p.379-392

1989

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Humans Use Directed and Random Exploration to Solve the Explore-Exploit Dilemma

Bayesian Online Learning of the Hazard Rate in Change-Point Problems

Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia

Proteomic Study of Low-Temperature Responses in Strawberry Cultivars (Fragaria × ananassa) That Differ in Cold Tolerance

Parallel Hopfield Networks

Viral suppressor proteins show varying abilities and effectiveness to suppress transgene-induced post-transcriptional gene silencing of endogenous Chalcone synthase in transgenic Arabidopsis

Two Novel Mutations Found in a Patient with 17α-Hydroxylase Enzyme Deficiency

Apparent mineralocorticoid excess

In Vitro Expression Studies of a Novel Mutation Δ299 in a Patient Affected with Apparent Mineralocorticoid Excess

Prenatal Diagnosis and Treatment of 11β-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Resulting in Normal Female Genitalia

Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia

Glucocorticoid resistance caused by reduced expression of the glucocorticoid receptor in cells from human vascular lesions

Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies

Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess

Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency

Commentary: The Education of a Faculty Developer

Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene

Several homozygous mutations in the gene for 11β-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess

Monogenic low renin hypertension : Endocrine hypertension

Distribution and abundance of marine bird and pinniped populations within Port Foster, Deception Island, Antarctica: Erupt: Ecosystem Studies at Deception Island, Antarctica

Profile of the pediatric endocrine clinic at New York-presbyterian hospital, New york weill cornell center

Characterization of PRP1 and PRP2 from Medicago truncatula

Autonomous Splicing and Complementation of in Vivo-Assembled Spliceosomes

A nodulin cDNA with homology to protochlorophyllide reductase

Complementation of in vitro-assembled spliceosomes

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