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sex chromosome aneuploidies, Turner syndrome, Klinefelter syndrome, pediatric endocrinology
United States

Activities

Employment (1)

University of Colorado: Denver, CO, US

Associate Professor (Pediatrics)
Employment
Source: Self-asserted source
Shanlee M. Davis

Education and qualifications (2)

University of Colorado: Aurora, CO, US

PhD
Education
Source: Self-asserted source
Shanlee M. Davis

Mayo Clinic Rochester: Rochester, MN, US

MD
Education
Source: Self-asserted source
Shanlee M. Davis

Funding (3)

Interrogating Fatty Acid Metabolism Impairment andClinical Correlates in Males with Klinefelter Syndrome

2022-07-01 to 2025-06-30 | Grant
National Institute of Diabetes and Digestive and Kidney Diseases (Bethesda, US)
GRANT_NUMBER: R01DK133292
Source: Self-asserted source
Shanlee M. Davis via DimensionsWizard

Population Health in Pediatric Sex Chromosome Aneuploidies

2020-09-01 to 2022-08-31 | Grant
Eunice Kennedy Shriver National Institute of Child Health and Human Development (Bethesda, US)
GRANT_NUMBER: R03HD102773
Source: Self-asserted source
Shanlee M. Davis via DimensionsWizard

TESTO: Testosterone Effects on Short-Term Outcomes in Infants with XXY

2017-09-01 to 2022-08-31 | Grant
Eunice Kennedy Shriver National Institute of Child Health and Human Development (Bethesda, US)
GRANT_NUMBER: K23HD092588
Source: Self-asserted source
Shanlee M. Davis via DimensionsWizard

Works (50 of 83)

Items per page:
Page 1 of 2

Prevalence and disease risks for male and female sex chromosome trisomies: a registry-based phenome-wide association study in 1.5 million participants of MVP, FinnGen, and UK Biobank

2025-02-02 | Preprint
Contributors: Shanlee M. Davis; Aoxing Liu; Craig C. Teerlink; Dana M. Lapato; Bryan Gorman; Giulio Genovese; Madhurbain Singh; Mary P. Reeve; Amanda Elswick Gentry; Kati M. Donner et al.
Source: check_circle
Crossref

Testosterone Effects on Short-Term Physical, Hormonal, and Neurodevelopmental Outcomes in Infants with 47,XXY/Klinefelter Syndrome: The TESTO Randomized Controlled Trial

2024-12-10 | Preprint
Contributors: Shanlee Davis; Susan Howell; Jennifer Janusz; Najiba Lahlou; Regina Reynolds; Talia Thompson; Karli Swenson; Rebecca Wilson; Judith Ross; Philip Zeitler et al.
Source: check_circle
Crossref

Infant gonadotropins predict spontaneous puberty in girls with Turner syndrome

2024-10 | Preprint
Contributors: Sawyer A; Bothwell S; Swenson K; Travers S; Davis S
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Generating Advancements in Longitudinal Analysis in X and Y Variations: Rationale, Design, and Methods for the GALAXY Registry

2024-08 | Preprint
Contributors: Carl A; Bothwell S; Swenson K; Bregante R; Cohen L; Cover V; Dawczyk A; Decker G; Gerken SB; Hong D et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Quantifying the Spectrum of Early Motor and Language Milestones in Sex Chromosome Trisomy

2024-08 | Preprint
Contributors: Thompson T; Bothwell S; Janusz J; Wilson R; Howell S; Davis S; Swenson K; Martin S; Kowal K; Ikomi C et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Research Priorities of Individuals and Families with Sex Chromosome Aneuploidies

2024-08 | Preprint
Contributors: Carl A; Bothwell S; Farah F; Swenson K; Hong D; Prakash S; Strang J; Tartaglia N; Raznahan A; Ross J et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Discordant Prenatal Cell-Free DNA Screening vs. Diagnostic Results of Sex Chromosome Aneuploidies: Implications for Newborn Screening and Genetic Counseling.

International journal of neonatal screening
2024-07 | Journal article
Contributors: Howell S; Davis SM; Carstens B; Haag M; Ross JL; Tartaglia NR
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Medical Findings in Infants Prenatally Identified with Sex Chromosome Trisomy in Year One of Life

2024-07 | Preprint
Contributors: Tartaglia N; Davis S; Howell S; Bothwell S; Nocon K; Kowal K; Ikomi C; Keene A; Reynolds V; Berglund A et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Mental Health Diagnoses and Suicidality Among Transgender Youth in Hospital Settings.

LGBT health
2024-07 | Journal article
Contributors: Nunes-Moreno M; Furniss A; Cortez S; Davis SM; Dowshen N; Kazak AE; Nahata L; Pyle L; Reirden DH; Schwartz B et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Prevalence, diagnostic features, and medical outcomes of females with Turner syndrome with a trisomy X cell line (45,X/47,XXX): Results from the InsighTS Registry.

American journal of medical genetics. Part A
2024-07 | Journal article
Contributors: Klamut N; Bothwell S; Carl AE; Bamba V; Law JR; Brickman WJ; Klein KO; Kanakatti Shankar R; Pinnaro CT; Fechner PY et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Clinical practice guidelines for the care of girls and women with Turner syndrome.

European journal of endocrinology
2024-06 | Journal article
Contributors: Gravholt CH; Andersen NH; Christin-Maitre S; Davis SM; Duijnhouwer A; Gawlik A; Maciel-Guerra AT; Gutmark-Little I; Fleischer K; Hong D et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Multicenter Analysis of Cardiometabolic-Related Diagnoses in Youth with Congenital Adrenal Hyperplasia: a PEDSnet study.

The Journal of clinical endocrinology and metabolism
2024-05 | Journal article
Contributors: Chen LM; Valentine A; Davis SM; Graber E; Fechner PY; Furniss A; Nahata L; Pyle L; Vyas AK; Vogiatzi MG et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

An extra X chromosome among adult women in the Million Veteran Program: A more benign perspective of trisomy X.

American journal of medical genetics. Part C, Seminars in medical genetics
2024-03 | Journal article
Contributors: Davis SM; Teerlink CC; Lynch JA; Klamut N; Gorman BR; Pagadala MS; Panizzon MS; Merritt VC; Genovese G; Ross JL et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Anxiety in Turner syndrome: Engaging community to address barriers and facilitators to diagnosis and care.

American journal of medical genetics. Part A
2024-03 | Journal article
Contributors: Carl A; Good M; Haag E; Hutaff-Lee C; Swain D; Tartaglia N; Sakamoto C; Davis S; Thompson T
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Prevalence, Morbidity, and Mortality of Men With Sex Chromosome Aneuploidy in the Million Veteran Program Cohort.

JAMA network open
2024-03 | Journal article
Contributors: Davis SM; Teerlink C; Lynch JA; Gorman BR; Pagadala M; Liu A; Panizzon MS; Merritt VC; Genovese G; Ross JL et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Development and validation of a computable phenotype for Turner syndrome utilizing electronic health records from a national pediatric network.

American journal of medical genetics. Part A
2023-12 | Journal article
Contributors: Huang SD; Bamba V; Bothwell S; Fechner PY; Furniss A; Ikomi C; Nahata L; Nokoff NJ; Pyle L; Seyoum H et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

The human Y and inactive X chromosomes similarly modulate autosomal gene expression.

Cell genomics
2023-12 | Journal article
Contributors: San Roman AK; Skaletsky H; Godfrey AK; Bokil NV; Teitz L; Singh I; Blanton LV; Bellott DW; Pyntikova T; Lange J et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

High Prevalence of Obstructive Sleep-Disordered Breathing in Pediatric Patients With Turner Syndrome.

Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
2023-11 | Journal article
Contributors: Pham TT; Davis SM; Tong S; Campa KA; Friedman NR; Gitomer SA
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Inspiring New Science to Guide Healthcare in Turner Syndrome: Rationale, design, and methods for the InsighTS Registry.

American journal of medical genetics. Part A
2023-10 | Journal article
Contributors: Kanakatti Shankar R; Carl A; Law JR; Bamba V; Brickman WJ; Prakash SK; Dowlut McElroy T; Howell S; Gutmark Little I; Klein KO et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Incidence, prevalence, age at diagnosis, and mortality in individuals with 45,X/46,XY mosaicism: A population-based registry study.

Genetics in medicine : official journal of the American College of Medical Genetics
2023-09 | Journal article
Contributors: Stochholm K; Holmgård C; Davis SM; Gravholt CH; Berglund A
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

The emotional journey of adapting to prenatally identified trisomy X.

Journal of genetic counseling
2023-09 | Journal article
Contributors: Thompson T; Tisher J; Davis S; Miller C; Kirk J; Tartaglia N; Howell S
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Development and Validation of a Computable Phenotype for Turner Syndrome Utilizing Electronic Health Records from a National Pediatric Network

2023-07 | Preprint
Contributors: Huang SD; Bamba V; Bothwell S; Fechner PY; Furniss A; Ikomi C; Nahata L; Nokoff NJ; Pyle L; Seyoum H et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Prevalence, Morbidity, and Mortality of 1,609 Men with Sex Chromosome Aneuploidy: Results from the Diverse Million Veteran Program Cohort

2023-07 | Preprint
Contributors: Davis SM; Teerlink C; Lynch JA; Gorman BR; Pagadala M; Liu A; Panizzon MS; Merritt VC; Genovese G; Pyarajan S et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

The human Y and inactive X chromosomes similarly modulate autosomal gene expression

2023-06 | Preprint
Contributors: San Roman AK; Skaletsky H; Godfrey AK; Bokil NV; Teitz L; Singh I; Blanton LV; Bellott DW; Pyntikova T; Lange J et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Information needs and health status in adolescents and young adults with differences of sex development or sex chromosome aneuploidies.

Journal of pediatric urology
2023-05 | Journal article
Contributors: Miller VA; Miller C; Davis SM; Nokoff NJ; Buchanan C; Friedrich EA; Carl A; Strine S; Vogiatzi MG
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Unique plasma metabolite signature for adolescents with Klinefelter syndrome reveals altered fatty acid metabolism.

Endocrine connections
2023-04 | Journal article
Contributors: Davis SM; Urban R; D'Alessandro A; Reisz JA; Chan CL; Kelsey M; Howell S; Tartaglia N; Zeitler P; Baker Ii P
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

The human inactive X chromosome modulates expression of the active X chromosome.

Cell genomics
2023-02 | Journal article
Contributors: San Roman AK; Godfrey AK; Skaletsky H; Bellott DW; Groff AF; Harris HL; Blanton LV; Hughes JF; Brown L; Phou S et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Neuropsychological and mental health concerns in a multicenter clinical sample of youth with turner syndrome.

American journal of medical genetics. Part A
2023-01 | Journal article
Contributors: Kremen J; Davis SM; Nahata L; Kapa HM; Dattilo TM; Liu E; Hutaff-Lee C; Tishelman AC; Crerand CE
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance.

Journal of genetic counseling
2022-10 | Journal article
Contributors: Howell S; Davis SM; Thompson T; Brown M; Tanda T; Kowal K; Alston A; Ross J; Tartaglia NR
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Multicenter Analysis of Cardiometabolic-related Diagnoses in Transgender and Gender-Diverse Youth: A PEDSnet Study.

The Journal of clinical endocrinology and metabolism
2022-09 | Journal article
Contributors: Valentine A; Davis S; Furniss A; Dowshen N; Kazak AE; Lewis C; Loeb DF; Nahata L; Pyle L; Schilling LM et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome.

American journal of obstetrics and gynecology
2022-07 | Journal article
Contributors: Dowlut-McElroy T; Davis S; Howell S; Gutmark-Little I; Bamba V; Prakash S; Patel S; Fadoju D; Vijayakanthi N; Haag M et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Hepatic abnormalities in youth with Turner syndrome.

Liver international : official journal of the International Association for the Study of the Liver
2022-07 | Journal article
Contributors: Singh I; Noel G; Barker JM; Chatfield KC; Furniss A; Khanna AD; Nokoff NJ; Patel S; Pyle L; Nahata L et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey.

Journal of school psychology
2022-06 | Journal article
Contributors: Thompson T; Davis S; Janusz J; Frith E; Pyle L; Howell S; Boada R; Wilson R; Tartaglia N
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Fertility Counseling Practices for Patients with Turner Syndrome in Pediatric Endocrine Clinics: Results of a Pediatric Endocrine Society Survey.

Hormone research in paediatrics
2022-04 | Journal article
Contributors: Theroux CI; Elliott V; Davis S; Crerand CE; Kremen J; Tishelman A; Hutaff-Lee C; Nahata L
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central
grade
Preferred source (of 2)‎

Population-based Assessment of Cardiometabolic-related Diagnoses in Youth With Klinefelter Syndrome: A PEDSnet Study

The Journal of Clinical Endocrinology & Metabolism
2022-04-19 | Journal article
Contributors: Shanlee M Davis; Natalie J Nokoff; Anna Furniss; Laura Pyle; Anna Valentine; Patricia Fechner; Chijioke Ikomi; Brianna Magnusen; Leena Nahata; Maria G Vogiatzi et al.
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

'I Wish the School Had a Better Understanding of the Diagnosis': parent perspectives on educational needs of students with sex chromosome aneuploidies.

Journal of research in special educational needs : JORSEN
2022-03 | Journal article
Contributors: Thompson T; Stinnett N; Tartaglia N; Davis S; Janusz J
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications.

Molecular genetics & genomic medicine
2021-11 | Journal article
Contributors: Howell S; Buchanan C; Davis SM; Miyazawa H; Furuta GT; Tartaglia NR; Nguyen N
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Non-Invasive Prenatal Testing (NIPT) Results for Participants of the eXtraordinarY Babies Study: Screening, Counseling, Diagnosis, and Discordance

2021-11 | Preprint
Contributors: Howell S; Davis SM; Thompson T; Brown M; Tanda T; Kowal K; Alston A; Ross J; Tartaglia NR
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Crinecerfont Lowers Elevated Hormone Markers in Adults with 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia.

The Journal of clinical endocrinology and metabolism
2021-10 | Journal article
Contributors: Auchus RJ; Sarafoglou K; Fechner PY; Vogiatzi MG; Imel EA; Davis SM; Giri N; Sturgeon J; Roberts E; Chan JL et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Behavioral Health Diagnoses in Youth with Gender Dysphoria Compared with Controls: A PEDSnet Study.

The Journal of pediatrics
2021-09 | Journal article
Contributors: Nunes-Moreno M; Buchanan C; Cole FS; Davis S; Dempsey A; Dowshen N; Furniss A; Kazak AE; Kerlek AJ; Margolis P et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

In-vivo skeletal muscle mitochondrial function in Klinefelter syndrome.

Journal of investigative medicine : the official publication of the American Federation for Clinical Research
2021-09 | Journal article
Contributors: Cung S; Pyle L; Nadeau K; Dabelea D; Cree-Green M; Davis SM
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Patient-parent perceptions of transition readiness in Turner syndrome and associated factors.

Clinical endocrinology
2021-09 | Journal article
Contributors: Patel N; Klamer B; Davis S; Nahata L
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Unique plasma metabolite signature for adolescents with Klinefelter syndrome reveals altered fatty acid metabolism

2021-09-02 | Preprint
Contributors: Shanlee M Davis; Rhianna Urban; Angelo D’Alessandro; Julie Haines; Christine Chan; Megan Kelsey; Susan Howell; Nicole Tartaglia; Philip Zeitler; Peter Baker, II
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

A gene-by-gene mosaic of dosage compensation strategies on the human X chromosome

2021-08 | Preprint
Contributors: San Roman AK; Godfrey AK; Skaletsky H; Bellott DW; Groff AF; Blanton LV; Hughes JF; Brown L; Phou S; Buscetta A et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Behavioral Health Diagnoses in Youth with Differences of Sex Development or Congenital Adrenal Hyperplasia Compared with Controls: A PEDSnet Study.

The Journal of pediatrics
2021-08 | Journal article
Contributors: Sewell R; Buchanan CL; Davis S; Christakis DA; Dempsey A; Furniss A; Kazak AE; Kerlek AJ; Magnusen B; Pajor NM et al.
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Changes in Adrenal and Gonadal Androgens After 14-Day Treatment With CRF1 Receptor Antagonist, Crinecerfont (NBI-74788), in Men With Classic 21-Hydroxylase Deficiency

Journal of the Endocrine Society
2021-05 | Journal article
Contributors: He X; Sarafoglou K; Fechner P; Vogiatzi M; Imel E; Davis S; Sturgeon J; Chan J; Farber R; Auchus R
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Clinical phenotype and management of individuals with mosaic monosomy X with Y chromosome material stratified by genital phenotype

American Journal of Medical Genetics Part A
2021-05 | Journal article
Contributors: Lindsey Guzewicz; Susan Howell; Canice E. Crerand; Hailey Umbaugh; Natalie J. Nokoff; Jennifer Barker; Shanlee M. Davis
Source: check_circle
Crossref
grade
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Multicenter Analysis of Cardiometabolic-Related Diagnosesin Transgender Adolescents

Journal of the Endocrine Society
2021-05 | Journal article
Contributors: Valentine A; Davis S; Dempsey A; Furniss A; Juarez-Colunga E; Pyle L; Reirden D; Nokoff N
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Cortical Bone Mass is Low in Boys with Klinefelter Syndrome and Improves with Oxandrolone.

Journal of the Endocrine Society
2021-02 | Journal article
Contributors: Vogiatzi MG; Davis SM; Ross JL
Source: Self-asserted source
Shanlee M. Davis via Europe PubMed Central

Neurodevelopmental and Mental Health Screening for Patients with Turner Syndrome in Pediatric Endocrine Clinics: Results of a Pediatric Endocrine Society Survey

Hormone Research in Paediatrics
2020 | Journal article
Contributors: Shanlee Davis; Canice Crerand; Christa Hutaff-Lee; Talia Thompson; Amy Tishelman; Omar Samara; Hailey Umbaugh; Leena Nahata; Jessica Kremen
Source: check_circle
Crossref
grade
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Items per page:
Page 1 of 2

Peer review (10 reviews for 7 publications/grants)

Review activity for Endocrine practice. (2)
Review activity for Endocrine reviews. (2)
Review activity for Heart and vessels. (1)
Review activity for Journal of the Endocrine Society. (1)
Review activity for The journal of clinical endocrinology and metabolism. (1)
Review activity for The Journal of pediatrics. (1)
Review activity for The Lancet regional health. (2)