Low Progesterone and Low Estradiol Levels Associate With Abdominal Aortic Aneurysms in Men

by Bergström, G., Langenskiöld, M., Nordanstig, J., NorlCrossed D Sign©n, A.-K, Ohlsson, C., Poutanen, M., Ryberg, H., Smidfelt, K., Tivesten, Å
Published 2022

Improving Familial Hypercholesterolemia Diagnosis Using an EMR-based Hybrid Diagnostic Model

by Eid, W.E, Lumpp, A., Miller, C., Sapp, E.H, Wendt, A.
Published 2022

Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases

by Dušátková, P., El Jellas, K., Fjeld, K., Groop, L., Haldorsen, I.S, Johansson, B.B, Johansson, S., Löhr, J.M, Molnes, J., Molven, A., Njølstad, P.R, Průhová, Š, Tjora, E.
Published 2022

Early-Pregnancy Intermediate Hyperglycemia and Adverse Pregnancy Outcomes Among Women Without Gestational Diabetes

by Li, X., Xiao, X., Xiong, Y., Ye, Y., Zhou, Q.
Published 2022

The Impact of Subclinical Hyperthyroidism on Cardiovascular Prognosis in Patients Undergoing Percutaneous Coronary Intervention

by Gao, J., Li, C., Liu, Y., Meng, X., Shao, C., Tang, Y.-D, Wang, W., Yang, J., Zhang, K., Zheng, Y., Zhou, Q.
Published 2022

Convolutional Neural Network-Based Computer-Assisted Diagnosis of Hashimoto's Thyroiditis on Ultrasound

by Kang, Q., Li, K., Ma, B., Qian, F., Zhao, W., Zhu, J.
Published 2022

Risk Factors for and Effects of Persistent and Severe Hypophosphatemia Following Ferric Carboxymaltose

by Schaefer, B., Wolf, M., Zoller, H.
Published 2022

Clinical Profiles and Genetic Spectra of 814 Chinese Children With Short Stature

by Chang, G., Chen, Y., Ding, Y., Huang, X., Li, J., Li, N., Li, Q., Li, X., Shen, Y., Song, C., Wang, J., Wang, X., Wang, Y., Yao, R., Zhang, H.
Published 2022

Physical Fitness and Cardiovascular Risk Factors in Novel Diabetes Subgroups

by Burkart, V., Gerdes, N., Kelm, M., Pesta, D.H, Roden, M., Saatmann, N., Strassburger, K., Szendroedi, J., Zaharia, O.-P
Published 2022

Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution

by Barroso, I., Bowker, N., Cai, L., Day, F.R, Dong, L., Glastonbury, C.A, Griffin, J.D, Kerrison, N.D, Koprulu, M., Langenberg, C., Li, C., Lotta, L.A, Luan, J., Lucarelli, D.M.E, McCarthy, M.I, O'Rahilly, S., Patel, S., Perry, J.R.B, Rocha, N., Saudek, V., Savage, D.B, Scott, R.A, Semple, R.K, Small, K.S, Stewart, I.D, Van De Streek, M., Wareham, N.J, Wheeler, E., Wittemans, L.B.L, Zhao, Y.
Published 2022

Impact of Cortisol on Reduction in Muscle Strength and Mass: A Mendelian Randomization Study

by Fukumoto, T., Iwahashi, N., Kaneko, H., Katsuhara, S., Matsuda, Y., Ogata, M., Ogawa, Y., Sakamoto, R., Terada, E., Umakoshi, H., Yokomoto-Umakoshi, M.
Published 2022

A Maternal Serum Metabolite Ratio Predicts Large for Gestational Age Infants at Term: A Prospective Cohort Study

by Charnock-Jones, D.S, Cook, E., Gaccioli, F., Goulding, N., Lawlor, D.A, McBride, N., Smith, G.C.S, Sovio, U.
Published 2022

A Longitudinal Study of Medial Temporal Lobe Volumes in Graves Disease

by Filipsson Nyström, H., Heckemann, R.A, Holmberg, M., Johansson, B., Klasson, N., Malmgren, H., Olsson, E., Skau, S., Starck, G.
Published 2022

Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome

by Chan, Y.-M, Hirschhorn, J.N, Laisk, T., Lindgren, C.M, Pujol-Gualdo, N., Wittemans, L.B.L, Zhu, J.
Published 2022

Sporadic Pseudohypoparathyroidism Type 1B in Monozygotic Twins: Insights into the Pathogenesis of Methylation Defects

by Bastepe, M., Hamasaki, A., Honjo, S., Iwasaki, K., Iwasaki, Y., Keidai, Y.
Published 2022

Novel Genomic Roadmaps and Their Clinical Translation Ahead

by Alexander, E.K
Published 2022

Bariatric Surgery: It's Not Just Incretins!

by Ferraz-Bannitz, R., Kashyap, S., Patti, M.E
Published 2022

Evaluation of Mineralocorticoid Receptor Antagonism on Changes in NT-proBNP among Persons with HIV

by Adler, G.K, Burdo, T.H, Defilippi, C., Fitch, K.V, Grinspoon, S.K, Iyengar, S., Shen, G., Srinivasa, S., Thomas, T.S, Walpert, A.R
Published 2022

First Japanese Family with PDX1-MODY (MODY4): A Novel PDX1 Frameshift Mutation, Clinical Characteristics, and Implications

by Aizawa-Abe, M., Enya, M., Hamasaki, A., Honjo, S., Horikawa, Y., Hosomichi, K., Iwasaki, K., Iwasaki, Y., Keidai, Y., Kubota, S., Yabe, D., Yoshiji, S.
Published 2022