L. Wiśniewski - Concepedia

Author

L. Wiśniewski

Icahn School of Medicine at Mount Sinai

Also Known As

L Wisniewski, L Wiśniewski, L. P. Wisniewski, L. Wisniewski, L. Wiśniewski, Lawrence P. Wisniewski, Lawrence Wisniewski

Publications

470

Citations

H-Index

Concepts

All Affiliations

Icahn School of Medicine at Mount Sinai University of Rochester Children's Memorial Health Institute KU Leuven Mount Sinai Medical Center

About

L. Wiśniewski is an author at Icahn School of Medicine at Mount Sinai specializing in medicine, genetics, and chromatin.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	212
2	Molecular Genetics	3	3	52
3	Public Health	1	1	14
4	Cell Biology	1	1	18
5	Molecular Biology	1	1	12

L. Wiśniewski

Publications

394

Citations

H-Index

Page 1

	Year	Citations
Cytogenetic and clinical studies in five cases of inv dup(15) L. Wiśniewski, Terry Hassold, James R. Heffelfinger, Human Genetics Cervical CancerNeurovirologyPathologyInv DupGynecology	1979	112
Prader‐Willi syndrome and a bisatellited derivative of chromosome 15 L. Wiśniewski, Mary E. Witt, Fredda Ginsberg‐Fellner, Clinical Genetics	1980	64
Acquired partial deletions of the long arm of chromosome 5 in hematologic disorders L. Wiśniewski, Kurt Hirschhorn American Journal of Hematology	1983	55
Partial tetrasomy 9 in a liveborn infant L. Wiśniewski, Gustavo D. Politis, Jerry Higgins Clinical Genetics	1978	39
Supernumerary microchromosomes identified as inverted duplications of chromosome 15: A report of three cases L. Wiśniewski, Richard A. Doherty Human Genetics ChromatinChromosome 15CytogeneticsSupernumerary MicrochromosomesGenetics	1985	26
Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: A variant example of the Lenz–Majewski syndrome Krystyńa Chrzańowska, J. P. Fryns, Małgorzata Krajewska‐Walasek, American Journal of Medical Genetics	1989	24
K562 human leukemia cell passages differ in embryonic globin gene expression Peter T. Rowley, Betsy M. Ohlsson‐Wilhelm, L. Wiśniewski, Leukemia Research Hematological MalignancyDevelopmental BiologyHematologyBlood CellGene Expression	1984	18
Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients Krystyńa Chrzańowska, J. P. Fryns, Małgorzata Krajewska‐Walasek, Clinical Genetics RheumatologyUnrelated PatientsCraniofacial DisorderMiller SyndromePhenotype Variability	1989	15
Anodontia as the sole clinical sign of the ectrodactyly-ectodermal dysplasia-cleft lip (EEC) syndrome. Chranowska Kh, Małgorzata Krajewska‐Walasek, Z Rump, PubMed Developmental AnomalyOligosymptomatic ExpressionEec SyndromeEctrodactyly-ectodermal Dysplasia-cleft LipCleft Lip	1990	15
An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies. L. Wiśniewski, G Purdy, T. Hassold, Journal of Medical Genetics CytogeneticsGeneticsPathologyMolecular GeneticsEmbryology	1977	14

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