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Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment

Molecular psychiatry, 2013-07, Vol.18 (7), p.781-787

2013

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New Insights into the Structural Characteristics of the Arabinogalactan−Protein (AGP) Fraction of Gum Arabic

Journal of agricultural and food chemistry, 2008-10, Vol.56 (19), p.9269-9276

2008

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apoplastic chitinase CpCHT1 isolated from the corolla of wintersweet exhibits both antifreeze and antifungal activities

Biologia plantarum, 2011-03, Vol.55 (1), p.141-148

2011

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Inflammation and metabolism gene sets in subcutaneous abdominal adipose tissue are altered 1 hour after exercise in adults with obesity

Journal of applied physiology (1985), 2021-10, Vol.131 (4), p.1380-1389

2021

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Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics

Molecular psychiatry, 2013-07, Vol.18 (7), p.739-739

2013

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Genetic association between endothelial nitric oxide synthase and Alzheimer disease

Clinical genetics, 2006-07, Vol.70 (1), p.49-56

2006

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BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

Blood cells, molecules, & diseases, 2015-03, Vol.54 (3), p.224-230

2015

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Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17

Hypertension (Dallas, Tex. 1979), 1999-07, Vol.34 (1), p.4-7

1999

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Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

American journal of human genetics, 1996-06, Vol.58 (6), p.1254-1259

1996

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Maternal component in the familial aggregation of hypertension

Clinical genetics, 2001-07, Vol.60 (1), p.13-21

2001

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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

The pharmacogenomics journal, 2007-12, Vol.7 (6), p.386-394

2007

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Identification and Characterization of GONST1, a Golgi-Localized GDP-Mannose Transporter in Arabidopsis

The Plant cell, 2001-10, Vol.13 (10), p.2283-2295

Baldwin, T. C.

2001

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Genetic predisposition to stroke in relatives of hypertensives

Stroke (1970), 2000-02, Vol.31 (2), p.487-492

2000

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Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia

Cellular and molecular biology (Noisy-le-Grand, France), 2004-02, Vol.50 (1), p.23

2004

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Single Base Mutation in the Type II Procollagen Gene (COL2A1) as a Cause of Primary Osteoarthritis Associated with a Mild Chondrodysplasia

Proceedings of the National Academy of Sciences - PNAS, 1990-09, Vol.87 (17), p.6565-6568

1990

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Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

Human molecular genetics, 1995-09, Vol.4 (9), p.1637-1642

1995

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Identification and Characterization of GONST1, a Golgi-Localized GDP-Mannose Transporter in Arabidopsis

The Plant cell, 2001-10, Vol.13 (10), p.2283-2295

2001

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Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab Community

American journal of human genetics, 2006-05, Vol.78 (5), p.871-877

2006

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Clinical and genetic correlates of soluble P‐selectin in the community

Journal of thrombosis and haemostasis, 2008-01, Vol.6 (1), p.20-31

2008

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Structure of cDNA clones coding for the entire preproα1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferences

Biochemical journal, 1989-06, Vol.260 (2), p.509-516

1989

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A new epidermal growth factor-like domain in the human core protein for the large cartilage-specific proteoglycan. Evidence for alternative splicing of the domain

The Journal of biological chemistry, 1989-09, Vol.264 (27), p.15747-15750

1989

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Autosomal Dominant Orthostatic Hypotensive Disorder Maps to Chromosome 18q

American journal of human genetics, 1998-11, Vol.63 (5), p.1425-1430

1998

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Molecular characteristics, association and interfacial properties of gum Arabic harvested from both Acacia senegal and Acacia seyal

Food hydrocolloids, 2016-12, Vol.61, p.514-522

2016

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Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations

Human genetics, 1998-05, Vol.102 (5), p.499-506

1998

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Linkage of early-onset osteoarthritis and chondrocalcinosis to human chromosome 8q

American journal of human genetics, 1995-03, Vol.56 (3), p.692-697

1995

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Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment

New Insights into the Structural Characteristics of the Arabinogalactan−Protein (AGP) Fraction of Gum Arabic

apoplastic chitinase CpCHT1 isolated from the corolla of wintersweet exhibits both antifreeze and antifungal activities

Inflammation and metabolism gene sets in subcutaneous abdominal adipose tissue are altered 1 hour after exercise in adults with obesity

Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics

Genetic association between endothelial nitric oxide synthase and Alzheimer disease

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

Maternal component in the familial aggregation of hypertension

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

Identification and Characterization of GONST1, a Golgi-Localized GDP-Mannose Transporter in Arabidopsis

Genetic predisposition to stroke in relatives of hypertensives

Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia

Single Base Mutation in the Type II Procollagen Gene (COL2A1) as a Cause of Primary Osteoarthritis Associated with a Mild Chondrodysplasia

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

Identification and Characterization of GONST1, a Golgi-Localized GDP-Mannose Transporter in Arabidopsis

Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab Community

Clinical and genetic correlates of soluble P‐selectin in the community

Structure of cDNA clones coding for the entire preproα1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferences

A new epidermal growth factor-like domain in the human core protein for the large cartilage-specific proteoglycan. Evidence for alternative splicing of the domain

Autosomal Dominant Orthostatic Hypotensive Disorder Maps to Chromosome 18q

Molecular characteristics, association and interfacial properties of gum Arabic harvested from both Acacia senegal and Acacia seyal

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations

Linkage of early-onset osteoarthritis and chondrocalcinosis to human chromosome 8q

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