M. Lippincott

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GWAS meta-analysis highlights the hypothalamic-pituitary-gonadal axis (HPG axis) in the genetic regulation of menstrual cycle length

R. Mägi, C. Lindgren, B. Neale, 2018, bioRxiv.

The genetic architecture of sporadic and multiple consecutive miscarriage

R. Mägi, A. Morris, D. Lawlor, 2020, Nature Communications.

The genetic architecture of sporadic and recurrent miscarriage

R. Mägi, A. Morris, D. Lawlor, 2019, bioRxiv.

Evaluating co‐created patient‐facing materials to increase understanding of genetic test results

S. Seminara, A. Dwyer, M. Lippincott, 2020, Journal of genetic counseling.

Large-scale meta-analysis highlights the hypothalamic–pituitary–gonadal axis in the genetic regulation of menstrual cycle length

R. Mägi, C. Lindgren, B. Neale, 2018, Human molecular genetics.

Predictors of endothelial function in employees with sedentary occupations in a worksite exercise program.

Kevin P. Smith, R. Cannon, A. Glaser, 2008, The American journal of cardiology.

Phenotypic spectrum of POLR3B mutations: isolated hypogonadotropic hypogonadism without neurological or dental anomalies

R. Quinton, S. Seminara, Y. Chan, 2016, Journal of Medical Genetics.

Continuous Kisspeptin Administration in Postmenopausal Women: Impact of Estradiol on Luteinizing Hormone Secretion

S. Seminara, Y. Chan, M. Lippincott, 2017, The Journal of clinical endocrinology and metabolism.

Use of genetic models of idiopathic hypogonadotrophic hypogonadism in mice and men to understand the mechanisms of disease

C. True, S. Seminara, M. Lippincott, 2013, Experimental physiology.

The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: Evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in vitro GAP activity assay.

R. Quinton, W. Crowley, A. Wilkie, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Hypothalamic Reproductive Endocrine Pulse Generator Activity Independent of Neurokinin B and Dynorphin Signaling.

I. Farooqi, T. Cole, R. Talbi, 2019, The Journal of clinical endocrinology and metabolism.

Assessing Sex Steroid Influence on Kisspeptin Responsiveness in Idiopathic Hypogonadotropic Hypogonadism

S. Seminara, Y. Chan, M. Lippincott, 2018, Journal of the Endocrine Society.

Discordance in the Dependence on Kisspeptin Signaling in Mini Puberty vs Adolescent Puberty: Human Genetic Evidence

V. Mericq, M. Shahab, S. Seminara, 2018, The Journal of clinical endocrinology and metabolism.

Kisspeptin Responsiveness Signals Emergence of Reproductive Endocrine Activity: Implications for Human Puberty.

J. Butler, S. Seminara, Y. Chan, 2016, The Journal of clinical endocrinology and metabolism.

Exogenous kisspeptin administration as a probe of GnRH neuronal function in patients with idiopathic hypogonadotropic hypogonadism.

J. Butler, S. Seminara, Y. Chan, 2014, The Journal of clinical endocrinology and metabolism.

Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system.

R. Quinton, S. Seminara, Y. Chan, 2014, The Journal of clinical endocrinology and metabolism.

Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism.

H. Brand, M. Talkowski, W. Crowley, 2022, The Journal of clinical endocrinology and metabolism.

Divergent responses to kisspeptin in children with delayed puberty.

S. Seminara, Y. Chan, Temitope O. Kusa, 2018, JCI insight.

Using Kisspeptin to Predict Pubertal Outcomes for Youth with Pubertal Delay.

S. Seminara, Y. Chan, Hector M Granados, 2020, The Journal of clinical endocrinology and metabolism.

Kisspeptin Overcomes GnRH Neuronal Suppression Secondary to Hyperprolactinemia in Humans

L. Nachtigall, S. Seminara, M. Lippincott, 2022, The Journal of clinical endocrinology and metabolism.

Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders.

Rany M Salem, Andrew Dauber, Joel N Hirschhorn, 2016, American journal of human genetics.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Ryan L. Collins, D. MacArthur, Daisuke Sato, 2017, Nature Genetics.

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.

Joel N Hirschhorn, Michael H. Guo, J. Hirschhorn, 2018, American journal of human genetics.

Microarray-Based Characterization of a Colony Assay Used to Investigate Endothelial Progenitor Cells and Relevance to Endothelial Function in Humans

J. P. McCoy, P. Munson, N. Raghavachari, 2009, Arteriosclerosis, thrombosis, and vascular biology.

Role of Inn1 and its interactions with Hof1 and Cyk3 in promoting cleavage furrow and septum formation in S. cerevisiae

E. Bi, J. Pringle, K. Moravcevic, 2009, The Journal of cell biology.

Relation of endothelial function to cardiovascular risk in women with sedentary occupations and without known cardiovascular disease.

Kevin P. Smith, R. Cannon, M. Waclawiw, 2008, The American journal of cardiology.