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:
Diversity and dysmorphology
Paul Kruszka, Cedrik Tekendo‐Ngongang, Maximilian Muenke
Current Opinion in Pediatrics (2019) Vol. 31, Iss. 6, pp. 702-707
Closed Access | Times Cited: 19
Paul Kruszka, Cedrik Tekendo‐Ngongang, Maximilian Muenke
Current Opinion in Pediatrics (2019) Vol. 31, Iss. 6, pp. 702-707
Closed Access | Times Cited: 19
Showing 19 citing articles:
Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)
Dena R. Matalon, Cinthya Zepeda‐Mendoza, Mahmoud Aarabi, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 6, pp. 100812-100812
Open Access | Times Cited: 25
Dena R. Matalon, Cinthya Zepeda‐Mendoza, Mahmoud Aarabi, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 6, pp. 100812-100812
Open Access | Times Cited: 25
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome
Sarah E. Sheppard, Ian M. Campbell, Margaret Harr, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 6, pp. 1649-1665
Open Access | Times Cited: 49
Sarah E. Sheppard, Ian M. Campbell, Margaret Harr, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 6, pp. 1649-1665
Open Access | Times Cited: 49
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16
Cedrik Tekendo‐Ngongang, Babajide Owosela, Nicole Fleischer, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 12, pp. 2939-2950
Closed Access | Times Cited: 25
Perspectives on the future of dysmorphology
Benjamin D. Solomon, Margaret P Adam, Chin‐To Fong, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 3, pp. 659-671
Closed Access | Times Cited: 15
Benjamin D. Solomon, Margaret P Adam, Chin‐To Fong, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 3, pp. 659-671
Closed Access | Times Cited: 15
Turner syndrome in diverse populations
Paul Kruszka, Yonit A. Addissie, Cedrik Tekendo‐Ngongang, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 2, pp. 303-313
Open Access | Times Cited: 21
Paul Kruszka, Yonit A. Addissie, Cedrik Tekendo‐Ngongang, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 2, pp. 303-313
Open Access | Times Cited: 21
Neural network classifiers for images of genetic conditions with cutaneous manifestations
Dat Duong, Rebekah L. Waikel, Ping Hu, et al.
Human Genetics and Genomics Advances (2021) Vol. 3, Iss. 1, pp. 100053-100053
Open Access | Times Cited: 16
Dat Duong, Rebekah L. Waikel, Ping Hu, et al.
Human Genetics and Genomics Advances (2021) Vol. 3, Iss. 1, pp. 100053-100053
Open Access | Times Cited: 16
Static and Motion Facial Analysis for Craniofacial Assessment and Diagnosing Diseases
Harold Matthews, Guido de Jong, Thomas Maal, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 19-42
Open Access | Times Cited: 8
Harold Matthews, Guido de Jong, Thomas Maal, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 19-42
Open Access | Times Cited: 8
An interactive atlas of three-dimensional syndromic facial morphology
J. David Aponte, Jordan J. Bannister, Hanne Hoskens, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 1, pp. 39-47
Open Access | Times Cited: 1
J. David Aponte, Jordan J. Bannister, Hanne Hoskens, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 1, pp. 39-47
Open Access | Times Cited: 1
Noonan syndrome on the African Continent
Cedrik Tekendo‐Ngongang, Paul Kruszka
Birth Defects Research (2020) Vol. 112, Iss. 10, pp. 718-724
Closed Access | Times Cited: 8
Cedrik Tekendo‐Ngongang, Paul Kruszka
Birth Defects Research (2020) Vol. 112, Iss. 10, pp. 718-724
Closed Access | Times Cited: 8
Cedrik Tekendo‐Ngongang, Sophie Dahoun, Séraphin Nguefack, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 4, pp. 619-622
Open Access | Times Cited: 7
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Research Square (Research Square) (2024)
Open Access
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Research Square (Research Square) (2024)
Open Access
Proof-of-principle neural network models for classification, attribution, creation, style-mixing, and morphing of image data for genetic conditions
Dat Duong, Rebekah L. Waikel, Ping Hu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 2
Dat Duong, Rebekah L. Waikel, Ping Hu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 2
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner Syndrome
Sarah E. Sheppard, Ian M. Campbell, Margaret Harr, et al.
Molecular Genetics and Metabolism (2021) Vol. 132, pp. S183-S183
Open Access | Times Cited: 1
Sarah E. Sheppard, Ian M. Campbell, Margaret Harr, et al.
Molecular Genetics and Metabolism (2021) Vol. 132, pp. S183-S183
Open Access | Times Cited: 1
Privacy, bias and the clinical use of facial recognition technology: A survey of genetics professionals
Elias Aboujaoude, Janice Light, Julia E. H. Brown, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access
Elias Aboujaoude, Janice Light, Julia E. H. Brown, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access
The Dysmorphic Infant
K. Taylor Wild, Sarah E. Sheppard, Elaine H. Zackai
Elsevier eBooks (2023), pp. 335-346.e1
Closed Access
K. Taylor Wild, Sarah E. Sheppard, Elaine H. Zackai
Elsevier eBooks (2023), pp. 335-346.e1
Closed Access
Essential Pieces to the Genetics Puzzle
Allison Tam
Pediatric Clinics of North America (2023) Vol. 70, Iss. 5, pp. 1047-1056
Closed Access
Allison Tam
Pediatric Clinics of North America (2023) Vol. 70, Iss. 5, pp. 1047-1056
Closed Access
Genetics 101
Alyce Belonis, Sofia Saenz Ayala
Pediatric Clinics of North America (2023) Vol. 70, Iss. 5, pp. 895-904
Closed Access
Alyce Belonis, Sofia Saenz Ayala
Pediatric Clinics of North America (2023) Vol. 70, Iss. 5, pp. 895-904
Closed Access
How to Select a Key Finding for a Syndrome Searching
Prashant Kumar Verma
Journal of Medical Evidence (2021) Vol. 2, Iss. 3, pp. 280-283
Open Access
Prashant Kumar Verma
Journal of Medical Evidence (2021) Vol. 2, Iss. 3, pp. 280-283
Open Access
