Author

S. M. Jalal

Observed names: S JALAL, S M Jalal, S. JALAL, S. Jalal, S. M. JALAL, S.M. Jalal, SM Jalal

Observed institutions: Agricultural Research Service, Mayo Clinic, United States Department of Agriculture, The University of Texas MD Anderson Cancer Center, University of Wisconsin–Madison, The University of Texas System, University of North Dakota

OpenAlex ID: A5111921408

Prognostic factors for hyperdiploid-myeloma: effects of chromosome 13 deletions and IgH translocations

2006 · W J Chng, R Santana-Dávila, et al. · Leukemia · 136

6q deletion in Waldenström macroglobulinemia is associated with features of adverse prognosis

2006 · E. M. Ocio, R. F. J. Schop, et al. · British Journal of Haematology · 120

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Tissue, cell type, and breast cancer stage-specific expression of a TGF-β inducible early transcription factor gene

1998 · M. Subramaniam, T.E. Hefferan, et al. · Journal of Cellular Biochemistry · 87

Euchromatic 9q+ heteromorphism in a family

1990 · S. M. Jalal, Mary K. Kukolich, et al. · American Journal of Medical Genetics · 74

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation

2003 · Dusica Babovic‐Vuksanovic, S.C. Jenkins, et al. · American Journal of Medical Genetics Part A · 66

Cytological differentiation of constitutive heterochromatin

1974 · S. M. Jalal, Roger W. Clark, et al. · Chromosoma · 54

Autism, profound mental retardation and atypical bipolar disorder in a 33‐year‐old female with a deletion of 15q12

1990 · J. KERBESHIAN, L. BURD, et al. · Journal of Intellectual Disability Research · 47

Partial 6p trisomy associated with infantile autism

1988 · Larry Burd, John T. Martsolf, et al. · Clinical Genetics · 43

2,4-D induced clastogenicity and elevated rates of sister chromatid exchanges in cultured human lymphocytes

1982 · C. Korte, S. M. Jalal · Journal of Heredity · 40

Increased rates of sister chromatid exchanges induced by the herbicide 2,4-D

1985 · T. E. Turkula, S. M. Jalal · Journal of Heredity · 35

Ploidy status rarely changes in myeloma patients at disease progression

2005 · W.J. Chng, J.M. Winkler, et al. · Leukemia Research · 33

Partial trisomy 7p associated with familial 7p;22q translocation.

1977 · L M Larson, W A Wasdahl, et al. · Journal of Medical Genetics · 33

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Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization

2001 · S. M. Jalal, M. E. Law, et al. · British Journal of Haematology · 30

Tetrasomy 9p: an emerging syndrome

1991 · S. M. Jalal, Mary K. Kukolich, et al. · Clinical Genetics · 29

Trisomy 22: No longer an enigma

1989 · Mary K. Kukolich, Anita Kulharya, et al. · American Journal of Medical Genetics · 29

Duplication 6q24 → 6qter in an infant from a balanced paternal translocation

1983 · T. R. Chase, S. M. Jalal, et al. · American Journal of Medical Genetics · 27

Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

1978 · L M Larson, W A Wasdahl, et al. · Journal of Medical Genetics · 24

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DDT-Induced Chromosomal Damage in Mice

1973 · GREGG A. JOHNSON, S. M. JALAL · Journal of Heredity · 24

Euchromatic 16p + heteromorphism: First report in North America

1990 · S. M. Jalal, Nancy R. Schneider, et al. · American Journal of Medical Genetics · 22

Familial transmission of 16p trisomy in an infant

1989 · S. M. Jalal, Donald W. Day, et al. · Human Genetics · 21

Subdivision of the human Y chromosome

1974 · S. M. Jalal, R. A. Pfeiffer, et al. · Human Genetics · 21

Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.

1987 · J. T. Martsolf, T. R. Chase, et al. · Clinical Genetics · 19

Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two nonmosaic daughters

1998 · D Babovic-Vuksanovic, J A Westman, et al. · Clinical Dysmorphology · 18

Two rare cases of 6p partial deletion

1989 · S. M. Jalal, Vincent R. Macias, et al. · Clinical Genetics · 18

De novo supernumerary ring chromosome 7: first report of a non‐mosaic patient and review of the literature

2002 · GVN Velagaleti, SM Jalal, et al. · Clinical Genetics · 17

Works count: 47

Citation count: 1,224

H-index: 21

I10-index: 31