Andrew K Poznanski

  • 3873 Citations
1956 …2009
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Personal profile

Research Interests

Dysmorphology

Certifications and Licenses

Radiology

Training Experience

1957Internship, Montreal General Hospital
1960Residency, Henry Ford Hospital

Education/Academic qualification

MD, McGill University

… → 1956

Research interests

  • Genetics: Medical
  • Medical Anthropology
  • Radiology

Fingerprint Dive into the research topics where Andrew K Poznanski is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
Hand Medicine & Life Sciences
Developmental Bone Disease Medicine & Life Sciences
Multiple Abnormalities Medicine & Life Sciences
Preschool Children Medicine & Life Sciences
Newborn Infant Medicine & Life Sciences
Wrist Medicine & Life Sciences
Bone and Bones Medicine & Life Sciences
Radiography Medicine & Life Sciences

Research Output 1956 2009

Variability of epilepsy, autism, brachydactyly, and other clinical features in familial and sporadic 2q37.3 deletion

Shrimpton, A. E., Kessler, J., Shaffer, L. G., Stack, C. V., Jalali, A., Little, R., Goldstein, J. L., Angle, B., Chary, A., Coppinger, J., Mathison, D. J., Khan, S., Poznanski, A. K., Dobyns, W. B., Craig, D. W., Hoo, J. J., Sarco, D. & Bassuk, A. G., Aug 3 2009, In : Journal of Pediatric Neurology. 7, 3, p. 279-283 5 p.

Research output: Contribution to journalArticle

Brachydactyly
Autistic Disorder
Epilepsy
Metacarpal Bones
Metatarsal Bones
80 Citations (Scopus)

Arthropathy of neonatal onset multisystem inflammatory disease (NOMID/CINCA)

Hill, S. C., Namde, M., Dwyer, A., Poznanski, A. K., Canna, S. & Goldbach-Mansky, R., Feb 1 2007, In : Pediatric Radiology. 37, 2, p. 145-152 8 p.

Research output: Contribution to journalArticle

Cryopyrin-Associated Periodic Syndromes
Joint Diseases
Knee
Mutation
Epiphyses
250 Citations (Scopus)

Nosology and classification of genetic skeletal disorders: 2006 Revision

Superti-Furga, A., Unger, S., Beighton, P., Bonafé, L., Braverman, N., Briggs, M., Cohn, D., Cormier-Dairé, V., Francomano, C., Hall, C., Horton, W., Kaitila, I., Krakow, D., Lachman, R., Lee, B., LeMerrer, M., Mortier, G., Mundlos, S., Nishimura, G., Poznanski, A. & 10 others, Rimoin, D., Robertson, S., Savarirayan, R., Spranger, J., Sillence, D., Warman, M., Wilcox, W., Wilkie, A., Zabel, B. & Zankl, A., Jan 1 2007, In : American Journal of Medical Genetics, Part A. 143, 1, p. 1-18 18 p.

Research output: Contribution to journalReview article

Developmental Bone Disease
Dysostoses
Inborn Genetic Diseases
Pedigree
Constitution and Bylaws
42 Citations (Scopus)

Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome

Zankl, A., Pachman, L. M., Poznanski, A. K., Bonafé, L., Wang, F., Shusterman, Y., Fishman, D. A. & Superti-Furga, A., Feb 1 2007, In : Journal of Bone and Mineral Research. 22, 2, p. 329-333 5 p.

Research output: Contribution to journalArticle

Matrix Metalloproteinase 2
Mutation
Genes
Gelatin
Hajdu-Cheney Syndrome
3 Citations (Scopus)

Lassoed liver: Hepatic pseudo-fissure caused by ventriculoperitoneal shunt

Chan, R. S. & Poznanski, A., Jan 1 2003, In : Pediatric radiology. 33, 1, p. 27-29 3 p.

Research output: Contribution to journalArticle

Ventriculoperitoneal Shunt
Catheters
Liver
Pathologic Processes
Abdomen