OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Pituitary Transcription Factor Mutations Leading to Hypopituitarism
Péter Gergics
Experientia supplementum (2019), pp. 263-298
Closed Access | Times Cited: 6
Péter Gergics
Experientia supplementum (2019), pp. 263-298
Closed Access | Times Cited: 6
Showing 6 citing articles:
High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency
Péter Gergics, Cathy Smith, Hironori Bando, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1526-1539
Open Access | Times Cited: 31
Péter Gergics, Cathy Smith, Hironori Bando, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1526-1539
Open Access | Times Cited: 31
NR5A1 c.991‐1G > C splice‐site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance
Maris Laan, Laura Kasak, Kęstutis Timinskas, et al.
Clinical Endocrinology (2020) Vol. 94, Iss. 4, pp. 656-666
Open Access | Times Cited: 17
Maris Laan, Laura Kasak, Kęstutis Timinskas, et al.
Clinical Endocrinology (2020) Vol. 94, Iss. 4, pp. 656-666
Open Access | Times Cited: 17
Dysgenesis and Dysfunction of the Pancreas and Pituitary Due toFOXA2Gene Defects
Sare Betül Kaygusuz, Esra Arslan Ateş, Maria Lillina Vignola, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 106, Iss. 10, pp. e4142-e4154
Open Access | Times Cited: 9
Sare Betül Kaygusuz, Esra Arslan Ateş, Maria Lillina Vignola, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 106, Iss. 10, pp. e4142-e4154
Open Access | Times Cited: 9
A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy
Diğdem Bezen, Orkide Kutlu, S. Mouilleron, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 9, pp. 2701-2706
Closed Access | Times Cited: 4
Diğdem Bezen, Orkide Kutlu, S. Mouilleron, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 9, pp. 2701-2706
Closed Access | Times Cited: 4
High-throughput splicing assays identify missense and silent splice-disruptivePOU1F1variants underlying pituitary hormone deficiency
Péter Gergics, Cathy Smith, Hironori Bando, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Péter Gergics, Cathy Smith, Hironori Bando, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency
P Gergics, C Smith, H Bando, et al.
Yearbook of pediatric endocrinology (2022)
Open Access
P Gergics, C Smith, H Bando, et al.
Yearbook of pediatric endocrinology (2022)
Open Access
