Peer-reviewed journal articles, book chapters, and selected abstracts.
Original communications in peer-reviewed medical and scientific journals.
Clinical validation of the Ion Torrent Oncomine Myeloid Assay GX v2 on the Genexus Integrated Sequencer as a stand-alone assay for single-nucleotide variants, insertions/deletions, and fusion genes.
Am J Clin Pathol, 2024Pitfalls of using PCR-based assays for JAK2 and CALR exon 9 variant testing in myeloproliferative neoplasms.
Am J Clin Pathol, 2023Medical students’ self-perceived knowledge and clinical comfort with genetics in Pakistan.
J Genet Couns, 2023Case report with cyto-histopathologic correlation and molecular findings. Sebastian A. Jofre, Maxwell Roth, Arash H Lahouti, Adam Gersten, Abul Kalam Azad, Robert D. Kelsch, Saeed Asiry, Yitzchak Goldstein, Rizwan Naeem, Rema Rao.
Diagn Cytopathol, 2022 • PMID: 35077030Results of a national survey on undergraduate genomics training (UTRIG Working Group). Haspel RL, Wilcox RL.
Genet Med, 2021 • PMID: 33580224Identifying current status and future needs through a web-based panel discussion. Myla Ashfaq, Syed A. Ahmed, Rabia Aziz-Rizvi, Zahra Hasan, Salman Kirmani, Shama Muneer, Rizwan Naeem, Jamal Raza, Aisha Furqan.
J Community Genet, 2023 • PMID: 32841689Presenting as isolated macrodactyly. Krishnamurthy K, Edema U, Ustun B, Villanueva-Siles E, Koehler SM, Naeem R, Wang Y, Goldstein DY.
J Surg Case Rep, 2023 • PMID: 37846420Karyotypic complexity and increased variants in next-generation sequencing associated with disease progression in T-cell leukemia/lymphoma cohort.
Int J Lab Hematol, 2022 • PMID: 33988304De novo mosaic and partial monosomy of chromosome 21 with superior vena cava duplication.
Mol Cytogenet, 2020 • PMID: 32944080Detection of silent carriers using novel TaqMan genotyping method.
Lab Med, 2020 • PMID: 31875889Underrepresentation of high-risk genotype in diverse populations.
Cytopathology, 2017HPV status and cytology correlation across specimen types.
Lab Med, 2017 • PMID: 28379422Epidermal mucinosis variant with spongiosis-like pattern.
J Cutan Pathol, 2015De novo 10.79 Mb deletion involving PAX8 gene causing hypothyroidism and mullerian agenesis.
Mol Cytogenet, 2014Comparison of pharmacogenetic vs clinical dosing algorithms.
N Engl J Med, 2013Long-term retrospective study in childhood and adolescence.
J Cutan Pathol, 2013Germline TP53 mutation and Li-Fraumeni syndrome association.
Arch Pathol Lab Med, 2010Zhang WW, Habeebu S, Sheehan AM, Naeem R, Hernandez VS, Dreyer ZE, LĂłpez-Terrada D.
J Pediatr Hematol Oncol, 2009Poland KS, Shardy DL, Azim M, Naeem R, Krance RA, Dreyer ZE, Neeley ES, Zhang N, Qiu H, Kornblau SM, Plon SE.
Genes Chromosomes Cancer, 2009Park HS, Park WS, Bondaruk J, Tanaka N, Katayama H, Lee S, Spiess PE, Steinberg JR, Wang Z, Katz RL, Dinney C, Elias KJ, Lotan Y, Naeem RC, Baggerly K, Sen S, Grossman HB, Czerniak B.
Journal publication, 2008Shinawi M, Erez A, Shardy DL, Lee B, Naeem R, Weissenberger G, Chinault AC, Cheung SW, Plon SE.
Blood, 2008Curry CV, Bishop MK, Hicks MJ, Naeem R, Reed JA, LĂłpez-Terrada DH. Diagnostic utility of fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction.
J Cutan Pathol, 2008Rabin KR, Man TK, Yu A, Folsom MR, Zhao Y, Rao PH, Plon SE, Naeem RC. Detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia.
Pediatr Blood Cancer, 2008Castillo A, Morse HC 3rd, Godfrey VL, Naeem R, Justice MJ.
Cancer Res, 2007Choi WT, Folsom MR, Azim M, Meyer C, Kowarz E, Marschalek R, Timchenko NA, Naeem RC, Lee DA.
Cancer Genet Cytogenet, 2007Poland KS, Azim M, Folsom M, Goldfarb B, Naeem R, Korch C, Drabkin HA, Gemmill RM, Plon SE.
Genes Chromosomes Cancer, 2007Qazilbash MH, Saliba RM, Ahmed B, Parikh G, Mendoza F, Ashraf N, Hosing C, Flosser T, Weber DM, Wang M, Couriel DR, Popat U, Kebriaei P, Alousi AM, Anderlini P, Naeem RC, Champlin RE, Giralt SA.
Biol Blood Marrow Transplant, 2007Powers JF, Tischler AS, Mohammed M, Naeem R. Genetic alterations in human pheochromocytomas.
Cancer Genet Cytogenet, 2005Orimo A, Gupta PB, Sgroi DC, Naeem R, Richardson AL, Weinberg RA. Recruitment of endothelial progenitor cells and angiogenesis.
Cell, 2005Sahoo T, Naeem R, Pham K, Chheng S, Noblin ST, Bacino CA, Gambello MJ. Unbalanced 10;18 chromosome translocation case report.
Am J Med Genet A, 2005Blackburn A, McLary C, Naeem R, Luszcz J, Stockton D, Donehower L, Mohammed M, Sofer T, Naber S, Otis C, Jerry D.
Cancer Res, 2004Yatsenko SA, Sahoo T, Rosenkranz M, Mendoza-Londono R, Naeem R, Scaglia F. Case report with unbalanced X;1 translocation.
Am J Med Genet, 2004Yusuf RZ, Naeem R. Relationship revisited in reproductive immunology.
Am J Reprod Immunol, 2004Duan Z, Duan Y, Lamendola DE, Yusuf RZ, Naeem R, Penson RT, Seiden MV. Resistance in paclitaxel/doxorubicin-treated cancer cells.
Clin Cancer Res, 2003Kuroiwa Y, Kasinathan P, Yoon JC, Naeem R, Tomizuka K, Sullivan EJ, Knott JG. Cloned calves expressing human immunoglobulin genes.
Nature Biotechnology, 2002Nash S, Marconi S, Sikorska K, Naeem R, Nash G. Evaluation in the era of genetic testing.
Am J Clin Pathol, 2002Marini T, Sullivan J, Naeem R. Screening results and informed consent improvements.
Am J Med Genet, 2002Luszcz J, Naeem R. Study based on New England Genetics Conference survey.
Journal of Genetic Technologists, 2002Bhargava R, Naeem R, Luszcz J, Marconi S, Garb J, Gasparini G, Otis C. Correlation with HER2 amplification.
Human Pathology, 2001Yusuf RZ, Naeem R. Comparative study of primary vs secondary culture methods.
Early Pregnancy Biology and Medicine, 2001Habecker-Green J, Naeem R, Scott RM, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn G.
Am J Med Genet, 2000Habecker-Green J, Naeem R, Gold H, O’Grady JP, Kanaan C, Bayer-Zwirello L.
Journal of Perinatology, 2000Habecker-Green J, Naeem R, Goh W, Pflueger S, Murray M, Cohn G.
Am J Med Genet, 1997Boyd T, Plevyak M, Christian J, Naeem R. Mechanism for enhanced intrauterine survival.
Modern Pathology, 1997Marini T, Pflueger S, Naber S, Karpells S, Naeem R.
Diagnostic Molecular Pathology, 1997Naeem R, Lux M, Huang S, Naber S, Corson J, Fletcher JA. Analysis of chromosome sequences.
Am J Pathology, 1996Naeem R, Samuel S, Fletcher JA. Cytogenetic analysis of t(8;13) translocation.
Genes Chromosomes and Cancer, 1995Fletcher J, Naeem R, Xiao S, Corson JM. Trisomy 8 as a predictor of recurrence in desmoid tumors.
Cancer Genetics Cytogenetics, 1994Naeem R, Donovan K, Corson JM, Fletcher JA. Fluorescent in situ hybridization in lung and kidney cells.
Cancer Genetics Cytogenetics, 1993Fletcher JA, Pinkus GS, Donovan K, Naeem R, Sugarbaker DJ, Metzger S. Chromosome band 6p21 rearrangement in mesenchymal component.
Cancer Research, 1992Naeem, R.C. In: Hu P, Hegde M, Madhuri L, Lennon PA (Eds). Chapter 17: Gene Rearrangements Testing.
Springer, 2012Naeem, R.C. In: Gersen S.L and Keagle M.B (Eds). Principles of Clinical Cytogenetics, 2nd Edition.
Humana Press, 2004OMICS and AI-driven drug repurposing for blast crises CML. Zafar Iqbal, Rizwan Naeem and others.
COAMS Research Day, Saudi Arabia, 2025RT-PCR vs NGS comparison in targeted therapies. Saeed Asiry, Abul Kalam Azad, Rizwan Naeem.
AMP, 2021Assessment of risk in hospitalized patients. Rizwan Naeem et al.
CAP21, 2021Identifying unnecessary duplicate testing in medical centers. Rizwan Naeem, Yitzchak Goldstein.
ACLPS Annual Meeting, 2021Distinct mutational profile in Caribbean population. Rizwan Naeem et al.
ASH Meeting, 2016High-risk HPV genotypes correlation in Bronx population. Rizwan Naeem et al.
American Society of Cytopathology, 2016Ethnically diverse population analysis. Rizwan Naeem et al.
AMP Annual Meeting, 2016SurePath vs ThinPrep correlation. Rizwan Naeem et al.
AMP Annual Meeting, 2015Performance comparison of viral detection assays. Rizwan Naeem et al.
AMP Annual Meeting, 2015Genetic analysis of inherited chromosomal deletion. Rizwan Naeem et al.
ASHG Meeting, 2014Comparison with Sanger sequencing. Rizwan Naeem et al.
AMP Meeting, 2014Respiratory virus panel assay comparison. Rizwan Naeem et al.
Yeshiva UniversityLinked to corpus callosum agenesis. Rizwan Naeem et al.
ASHG Meeting, 2014Chromosome 11 abnormalities in MDS case. Rizwan Naeem et al.
Hematopathology Workshop, 2013PAX8 gene related findings. Rizwan Naeem et al.
ACMG Meeting, 2014Multiplex autistic family evaluation. Rizwan Naeem et al.
ACMG Meeting, 2014Duplication and deletion abnormalities. Rizwan Naeem et al.
ACMG Meeting, 2014Performance of Simplexa RT-PCR assay. Rizwan Naeem et al.
IDWeek Conference, 2013Complex chromosomal rearrangements analysis. Rizwan Naeem et al.
ACMG Meeting, 2013Improved accuracy and precision of genomic testing through sequential quality-control measures in personalized medicine: improving the reliability and precision of array CGH testing in personalized medicine. Brandon Schein, Jianli Li and Rizwan Naeem.
Albert Einstein College of Medicine Students Day, Bronx, NY, August 2012A platform-neutral clinical cancer genomics database. The first database draft from >1800 clinical cases collected from 17 cytogenetics laboratories. Rizwan C. Naeem et al.
CCMC Meeting, Chicago, IL, August 6–7, 2012Results and experiences involving microarray-based comparative genomic hybridization (aCGH) in an inner-city setting. Rizwan Naeem et al.
ASHG Meeting, Montreal, Canada, October 2011Comparing two different platforms for analyzing genomic DNA micro-array in mental retardation. Rizwan Naeem et al.
USCAP Meeting, San Antonio, TX, February 201111q23 loss as a potential independent genetic marker in neuroblastoma without MYCN amplification. R. Naeem et al.
Denver, CO, May 2007Characterization of a novel chromosomal translocation in a pediatric patient with acute myelogenous leukemia. Naeem RC et al.
Pediatr Blood Cancer, 2006Clear cell sarcoma of soft tissue with cytogenetic and molecular analyses. R. Naeem et al.
Dermatopathology Conference, Houston, TX, August 2006Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia. Rizwan Naeem et al.
Blood, 2006C/EBP suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL. Rizwan C. Naeem et al.
ASH Meeting, Houston, TX, 2006A balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to renal cell cancer. R. Naeem et al.
ACMG Meeting, 2005Strategies of increase detection of cytogenetic markers in childhood acute leukemia: need for standardized testing. R. Naeem et al.
Association of Molecular Pathology Meeting, 2005Identification of the novel chromosomal translocation t(17;19)(q23;q13) in a pediatric patient with acute myeloid leukemia. R.C. Naeem et al.
American Society of Hematology Meeting, 2005Clear cell sarcoma of soft tissue with cytogenetic and molecular analyses. R. Naeem et al.
American Society of Dermatopathology Meeting, 2005Improving cytogenetic abnormality rate to 100% in childhood acute leukemia. R. Naeem et al.
Pediatric Hematology Oncology Meeting, 2005Characterization of a novel chromosomal translocation in pediatric AML. R.C. Naeem et al.
Pediatric Hematology Oncology Meeting, 2005Improving cytogenetic abnormality rate in childhood acute leukemia. R. Naeem et al.
Washington DC Meeting, 2005Strategies to increase detection of cytogenetic markers in childhood leukemia. R. Naeem et al.
Los Angeles, CA, 2004Analysis of chromosomal instability in pediatric neuroblastoma. Naeem R.
Baylor Cancer Center Symposium, 2003State-of-the-art diagnostic cancer cytogenetics and molecular laboratory. Naeem R. et al.
Baylor Cancer Center Retreat, 2003Mechanisms of tumorigenesis in mammary tumors from BALB/c-Trp53 heterozygous mice. R. Naeem et al.
ASHG Meeting, Baltimore, 2002Preliminary validation of genomic microarrays for routine prenatal screening. R. Naeem et al.
ASHG Meeting, Baltimore, 2002Phenotypic consequences in a child with de novo X;1 translocation. R. Naeem et al.
ASHG Meeting, 2002Subtelomeric FISH analysis: recent experience and referral trends in a clinical cytogenetics laboratory. R. Naeem et al.
ASHG Meeting, Baltimore, 2002R. Saleki, C. Bacino, J. Wu, M. Santini, R. Naeem. Novel subtelomeric rearrangements of human chromosomes detected by telomere FISH.
ASHG Annual Meeting, October 2002, Baltimore, MarylandT. Sahoo, R. Naeem, K. Pham, S. Cheng, S. Noblin, C. Bacino and M. Gambello. Unusual phenotype and cytogenetic features in a case of trisomy 18 due to isochromosome 18q: clinical, cytogenetic and molecular characterization.
ASHG Annual Meeting, October 2002, Baltimore, MarylandJ. Grund, A. Asamoah, D. VanDyke, R. Naeem. Deletion of 8q24.13–q24.21 associated with macrocephaly, developmental delay, and multiple minor anomalies.
American College of Medical Genetics Meeting, March 2002, New Orleans, LouisianaR. Naeem, R. Bhargava, M. Karamian, R. Hasserjian. Significance of double minute in a case of acute megakaryoblastic leukemia (M7).
AJHG Supplement, October 2001R. Bhargava, R. Naeem, S. Marconi, J. Luszcz, R. Gasparini, C. Otis. Tyrosine activation in breast carcinoma with correlation to HER-2/neu gene amplification.
AJHG Supplement, October 2001V. Ramay, F. Bsat, R. Naeem, G. Cohn. Ultrasound diagnosis of a sacrococcygeal teratoma leading to prenatal diagnosis of Jacobsen syndrome.
AJHG Supplement, October 2001I. Rouse, T. Marini, D. Grow, P. Pekow, P. Nasca, R. Naeem. Down syndrome screening in in-vitro fertilization pregnancies: is there a need for a HCG adjustment factor?
AJHG Supplement, October 2001K.L. Hickey, R. Hasserjian, C. Andrzejewski, R. Naeem. Chromosomal alterations associated with autologous peripheral stem cell transplantation treated acute myeloid leukemia.
Association of Molecular Pathologists Meeting, 2001V. Loik Ramey, F. Bsat, R. Naeem, G.M. Cohn. Ultrasound diagnosis of a sacrococcygeal teratoma leading to prenatal diagnosis of Jacobsen syndrome.
AJHG Supplement, October 2001S. Ahmed, A. Anguiano, R. Bhargava, J. Smith, R. Lorenzana, R. Naeem. Cytogenetic & SKY multicolor FISH characterization of malignant mesenchymoma.
Annual Clinical Genetics Meeting, March 2001, Miami, FLS. Ahmed, J. Sullivan, R. Naeem. Presence of XX/XY cell lines in primary amniotic fluid cultures: diagnostic dilemma and follow-up.
Annual Clinical Genetics Meeting, March 2001, Miami, FLJ.G. Habecker-Green, V.L. Ramie, R. Naeem, G.M. Cohn. Partial trisomy 12 and 13 in a newborn.
AJHG, October 2000, ASHG Meeting Philadelphia, PAR. Naeem, G.M. Cohn, D.J. Cardeiro, J.G. Habecker-Green. Repeat karyotypic analysis may be periodically indicated.
AJHG, October 2000, ASHG Meeting Philadelphia, PAE.L. Habecker, J.G. Habecker-Green, R. Naeem, G.M. Cohn. Amniocentesis rates in women of Puerto Rican ethnicity.
AJHG, October 2000, ASHG Meeting Philadelphia, PAJ.C. Sullivan, T. Marini, R. Greenwood, R. Blatt, R. Naeem. A comprehensive genetic laboratory database for public health planning.
AJHG, October 2000, ASHG Meeting Philadelphia, PAJ.M. Luszcz, R. Naeem. Current views on continuing education and employee awareness assessed by questionnaire.
AJHG, October 2000, ASHG Meeting Philadelphia, PAS.P. Naber, M. Karamov, C. Phillips, A. Nasir, R. Naeem. RX FISH in conjunction with G-banding for resolving complex chromosomal rearrangements.
AJHG, October 2000, ASHG Meeting Philadelphia, PAT. Marini, J. Sullivan, R. Naeem, E. Reiter. Response to growth hormone therapy in a patient with 15q deletion.
AJHG, October 2000, ASHG Meeting Philadelphia, PAJ. Sullivan, R. Yusuf, T. Marini, R. Naeem. Double and triple trisomy in spontaneous abortion.
Clinical Genetics Meeting, March 2000, Palm Springs, CAR.Z. Yusuf, A. Juozokas, S. Kellman, R. Naeem. Cytogenetic analysis of products of conception: comparison of two culture methods.
International Medical Sciences Congress, Istanbul, Turkey, April 1999R. Naeem, A.H. Jackson, G. Cohn, J. Sullivan. Deletion 2q37.1 in a child with familial paroxysmal kinesigenic choreoathetosis.
ASHG Annual Meeting, October 1999, San Francisco, CAJ.C. Sullivan, G. Cohn, T. Marini, R. Naeem. Should patients with a triploid pregnancy be offered prenatal diagnosis in subsequent pregnancies?
ASHG Meeting, October 1999, San Francisco, CAJ. Habecker-Green, R. Naeem, S. Pflueger, J.P. O’Grady. Prenatal diagnosis of trisomy 8 mosaicism.
ASHG Meeting, October 1999, San Francisco, CAJ. Sullivan, M. Murray, A. Ratti, T. Marini, R. Naeem. An unusual case of pseudodicentric Xq and possible mechanism.
ACMG Meeting, March 1999, Miami, FLG. Hostetter, J. Freeman, R. Naeem. Dermatofibrosarcoma protuberans with complex chromosomal findings.
ACMG Meeting, March 1999, Miami, FLMarini J., Sullivan J., Murray M., Kanaan C., Boyd T., R. Naeem. Implications of atypical biochemical data in a case of presumed anencephaly.
ACMG March 1999 Meetings, Miami, FLR. Naeem, C. Kanaan, T. Marini, A. Romanyshyn, S. Pflueger, J. Sullivan. Prenatal detection of trisomy 2 (q35q36) with elevated MSAFP.
ASHG Annual Meeting, October 1998, Denver, COMarini J., Sullivan J., Shields J., Pflueger S., Naber S., R. Naeem. Poor utilization of maternal serum screening by advanced maternal age patients.
ASHG Annual Meeting, October 1998, Denver, COJ. Sullivan, T. Marini, J. Christian, G. Cohn, S. Naber, R. Naeem. Monosomy 21 and derivative chromosome 5: a distinct clinical syndrome.
ASHG Annual Meeting, October 1998, Denver, COR. Naeem, J. Habecker-Green, G. Cohn. De novo translocation (8;12): clinical features and implications.
March of Dimes & ACMG Meeting, February 1998, Los Angeles, CAR. Naeem, A. Romanyshyn, T. Boyd. Consistent secondary chromosomal changes in cases of alveolar rhabdomyosarcoma.
March of Dimes & ACMG Meeting, February 1998, Los Angeles, CASullivan A., Ratti A., Moskovitz A., R. Naeem. Prenatal detection and follow-up of mosaic partial trisomy 14.
March of Dimes & ACMG Meeting, February 1998, Los Angeles, CASullivan S., Pflueger S., Marini T., Karamov M., R. Naeem. De novo interstitial deletion 6 (q13q21).
March of Dimes & ACMG Meeting, February 1998, Los Angeles, CABoyd M., Plevyak J., Christian J., R. Naeem. Confined placental mosaicism as mechanism for enhanced intrauterine survival.
US & Canadian Academy of Pathology Meeting, March 1997, Orlando, FLJ.C. Sullivan, H. Dineen, D. Grow, M. Arny, R. Naeem. Five-year experience with prenatal diagnosis after assisted reproduction.
American Journal of Human Genetics, 1996C.D. Amato, R. Naeem. Fluorescence in-situ hybridization (FISH) on uncultured amniocytes.
AGT Annual Meeting 1996R. Naeem, R. Heptulla, C. Andries, C. Otis. Presence of Y-chromosome in gonadoblastoma.
US & Canadian Academy of Pathology, March 1996C.N. Otis, R. Naeem, J. Donovan, J.L. Powell, M. Prefontane. Trisomy 12 in ovarian granulosa tumors.
Pathology Meeting, March 1996R. Naeem, D. Federman. Confirmation of first human Y/autosome translocation.
Clinical Genetics Meeting, March 1996, TexasJ. Sullivan, S. Pflueger, R. Naeem. Uniparental disomy in cases of marker chromosomes.
American Journal of Human Genetics, 1995R. Naeem, M. Lux, S. Huang, S. Naber. Characterization of ring chromosome in dermatofibrosarcoma.
AJHG, 1995White L., Derkaloustian V., Naeem R., Knoll J. Chromosome 15 duplications: mechanism of formation.
AJHG, 1995Habecker-Green J., Kanan C., Bayer-Zwirello L., O’Grady J., R. Naeem. Clinical follow-up of trisomy 18 mosaicism.
AJHG, 1995Ratti K., Schwartz, R. Naeem. Isodisomy explanation for genotype discrepancies.
Cytogenetic Technologists Meeting, 1995Heptulla R., Naeem R., Otis C. PCR-mediated detection of Y chromosome in gonadoblastomas.
Endocrine Society Meeting, 1995R. Bernier, R. Naeem. Semi-automated solid tumor harvesting.
Cytogenetic Technologists Meeting, 1995Sullivan L., Bayer-Zwirello L., R. Naeem. Genotype-phenotype correlation in mosaic tetrasomy 18p.
Clinical Genetics Conference, 1995R. Naeem, J.A. Fletcher, S. Naber. Detection of trisomy 8 in fibromatosis using FISH.
Modern Pathology, 1994R. Naeem, J.A. Fletcher, C. Andreis, S. Naber. Cytogenetic characterization of fibromatoses.
European Society of Human Genetics, 1994Golden R., Ratti K.A., R. Naeem. Characterizing marker chromosomes in amniocentesis.
Association of Cytogenetic Technologists, 1994Schwartz, R. Naeem. Translocation and trisomy in biphenotypic leukemia.
Cytogenetic Technologists Meeting, 1994Schwartz A., Ratti, R. Naeem. Comparison of FISH technologies.
Cytogenetic Technologists Meeting, 1994R. Naeem, J.A. Fletcher, S.P. Andreis. Cytogenetic characterization of fibroproliferative lesions.
Clinical Genetics Conference, 1994R. Naeem, J.A. Fletcher. Translocation (8;13) in stem cell leukemia.
AJHG, 1993R. Naeem, J.A. Fletcher. Novel FISH approach on paraffin tissues.
Applied Cytogenetics, 1993R. Naeem. Registry of birth defects in Karachi, Pakistan.
Genetic Epidemiology Society, 1993R. Naeem, J.A. Fletcher. Translocation involving T-cell and myeloid lineages.
ASHG Annual Meeting, 1993R. Naeem, J.A. Fletcher. Trisomy 8 as a genetic marker in desmoid tumors.
AJHG, 1992