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Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach.
Published in:
Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29932-y
By:
- Richardson, Tom G.;
- Crouch, Daniel J. M.;
- Power, Grace M.;
- Morales-Berstein, Fernanda;
- Hazelwood, Emma;
- Fang, Si;
- Cho, Yoonsu;
- Inshaw, Jamie R. J.;
- Robertson, Catherine C.;
- Sidore, Carlo;
- Cucca, Francesco;
- Rich, Steven S.;
- Todd, John A.;
- Davey Smith, George
Publication type:
Article
Familial aggregation of nasopharyngeal carcinoma and other malignancies. A clinicopathologic description.
Published in:
1991
By:
- Coffin, Cheryl M.;
- Rich, Steven S.;
- Dehner, Louis P.;
- Coffin, C M;
- Rich, S S;
- Dehner, L P
Publication type:
journal article
Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin.
Published in:
2003
By:
- Bergman, Richard N.;
- Zaccaro, Daniel J.;
- Watanabe, Richard M.;
- Haffner, Steven M.;
- Saad, Mohammed F.;
- Norris, Jill M.;
- Wagenknecht, Lynne E.;
- Hokanson, James E.;
- Rotter, Jerome I.;
- Rich, Steven S.
Publication type:
journal article
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).
Published in:
Human Molecular Genetics, 1999, v. 8, n. 12, p. 2325, doi. 10.1093/hmg/8.12.2325
By:
- Sahoo, Trilochan;
- Johnson, Eric W.;
- Thomas, James W.;
- Kuehl, Peter M.;
- Jones, Thomas L.;
- Dokken, Charles G.;
- Touchman, Jeffrey W.;
- Gallione, Carol J.;
- Lee-Lin, Shih-Queen;
- Kosofsky, Barry;
- Kurth, Janice H.;
- Louis, David N.;
- Mettler, Gabrielle;
- Morrison, Leslie;
- Gil-Nagel, Antonio;
- Rich, Steven S.;
- Zabramski, Joseph M.;
- Boguski, Mark S.;
- Green, Eric D.;
- Marchuk, Douglas A.
Publication type:
Article
Homozygous parent affected sib pair method for detecting disease predisposing variants: Application to insulin dependent diabetes mellitus.
Published in:
Genetic Epidemiology, 1993, v. 10, n. 5, p. 273, doi. 10.1002/gepi.1370100502
By:
- Robinson, Wendy P.;
- Barbosa, Jose;
- Rich, Steven S.;
- Thomson, Glenys
Publication type:
Article
A gene responsible for cavernous malformations of the brain maps to chromosome 7q.
Published in:
Human Molecular Genetics, 1995, v. 4, n. 3, p. 453
By:
- Dubovsky, Jan;
- Zabramski, Joseph M.;
- Kurth, Janice;
- Spetzier, Robert F.;
- Rich, Steven S.;
- Orr, Harry T.;
- Weber, James L.
Publication type:
Article

Found: 6

Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach.

Familial aggregation of nasopharyngeal carcinoma and other malignancies. A clinicopathologic description.

Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin.

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).

Homozygous parent affected sib pair method for detecting disease predisposing variants: Application to insulin dependent diabetes mellitus.

A gene responsible for cavernous malformations of the brain maps to chromosome 7q.