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...
Absence of linkage between familial neural tube defects and PAX3 gene (1995)
Mariman, E.C.M., Johnson, W.G., Hamel, B.C.J., Koenigsberger, M.R., Stenroos, E.S., Geurds, M.P.A., ...
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...
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...
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...
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...
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...
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...
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...
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.
Shugart, Y Y, Banerjee, P, Knowles, J A, Lewis, C A, Jacobson, S G, Matise, T C, ...
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,...
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...