Y. Y. Shugart

Publication List Details

Period

1995 - 2006

Number

19

Co-Authors

Effect of the peroxisome proliferators-activated receptor (PPAR) gamma 3 gene on BMI in 1,210 school students from Morelos, Mexico (2006)

Chen, L., Velasco Mondragon, H.E., Lazcano-Ponce, E., Collins, A., Shugart, Y.Y.

Little research has been undertaken on risk factors for obesity in young people in Latin America, including Mexico, despite the fact that obesity constitutes the number one public health problem in...

Complex Segregation Analysis Provides Compelling Evidence for a Major Gene Underlying Obsessive-Compulsive Disorder and for Heterogeneity by Sex

Nestadt, G., Lan, T., Samuels, J., Riddle, M., Bienvenu III, O. J., Liang, K. Y., ...

Evidence from twin and family studies supports a genetic etiology for obsessive-compulsive disorder (OCD). The purpose of this study was to test whether a major gene is implicated in a proportion of...

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.

Bignell, G R, Canzian, F, Shayeghi, M, Stark, M, Shugart, Y Y, Biggs, P, ...

Thyroid goiter is a common condition that is often associated with iodine deficiency. Familial forms of goiter in areas not known to feature iodine deficiency are much less common. We have performed...

Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.

Giraud, S, Zhang, C X, Serova-Sinilnikova, O, Wautot, V, Salandre, J, Buisson, N, ...

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome predisposing to tumors of the parathyroid, endocrine pancreas, anterior pituitary, adrenal glands, and diffuse...

Linkage analysis in familial Angelman syndrome.

Wagstaff, J, Shugart, Y Y, Lalande, M

Familial Angelman syndrome (AS) can result from mutations in chromosome 15q11q13 that, when transmitted from father to child, result in no phenotypic abnormality but, when transmitted from mother to...

Complex Segregation Analysis Provides Compelling Evidence for a Major Gene Underlying Obsessive-Compulsive Disorder and for Heterogeneity by Sex

Nestadt, G., Lan, T., Samuels, J., Riddle, M., Bienvenu III, O. J., Liang, K. Y., ...

Evidence from twin and family studies supports a genetic etiology for obsessive-compulsive disorder (OCD). The purpose of this study was to test whether a major gene is implicated in a proportion of...

Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.

Giraud, S, Zhang, C X, Serova-Sinilnikova, O, Wautot, V, Salandre, J, Buisson, N, ...

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome predisposing to tumors of the parathyroid, endocrine pancreas, anterior pituitary, adrenal glands, and diffuse...

Linkage analysis in familial Angelman syndrome.

Wagstaff, J, Shugart, Y Y, Lalande, M

Familial Angelman syndrome (AS) can result from mutations in chromosome 15q11q13 that, when transmitted from father to child, result in no phenotypic abnormality but, when transmitted from mother to...

Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

Serova, O M, Mazoyer, S, Puget, N, Dubois, V, Tonin, P, Shugart, Y Y, ...

To estimate the proportion of breast cancer families due to BRCA1 or BRCA2, we performed mutation screening of the entire coding regions of both genes supplemented with linkage analysis of 31...

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.

Bignell, G R, Canzian, F, Shayeghi, M, Stark, M, Shugart, Y Y, Biggs, P, ...

Thyroid goiter is a common condition that is often associated with iodine deficiency. Familial forms of goiter in areas not known to feature iodine deficiency are much less common. We have performed...

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Kumar, S, Kimberling, W J, Gabow, P A, Shugart, Y Y, Pieke-Dahl, S

Autosomal dominant polycystic kidney disease is a heritable disorder and recent studies have shown genetic heterogeneity, with some, but not all, families showing linkage with markers on chromosome...

Absence of linkage between familial neural tube defects and PAX3 gene.

Chatkupt, S, Hol, F A, Shugart, Y Y, Geurds, M P, Stenroos, E S, Koenigsberger, M R, ...

Neural tube defects (NTD) are among the most common and disabling birth defects. The aetiology of NTD is unknown and their genetics are complex. The majority of NTD cases are sporadic, isolated,...

PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.

Hol, F A, Geurds, M P, Chatkupt, S, Shugart, Y Y, Balling, R, Schrander-Stumpel, C T, ...

From studies in the mouse and from the clinical and molecular analysis of patients with type 1 Waardenburg syndrome, particular members of the PAX gene family are suspected factors in the aetiology...