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RS Sparkes

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Noble E P; Zhang X; Ritchie T L; Sparkes R S
Haplotypes at the DRD2 locus and severe alcoholism.
Delgado-Escueta A V; Medina M T; Serratosa J M; Castroviejo I P; Gee M N; Weissbecker K; Westling B W; Fong C Y; Alonso M E; Cordova S; Shah P; Khan S; Sainz J; Rubio-Donnadieu F; Sparkes R S
Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
Noble E P; Zhang X; Ritchie T; Lawford B R; Grosser S C; Young R M; Sparkes R S
D2 dopamine receptor and GABA(A) receptor beta3 subunit genes and alcoholism.

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All Publications

2000: Noble E P; Zhang X; Ritchie T L; Sparkes R S
Haplotypes at the DRD2 locus and severe alcoholism.
American journal of medical genetics 2000;96(5):622-31.
1999: Delgado-Escueta A V; Medina M T; Serratosa J M; Castroviejo I P; Gee M N; Weissbecker K; Westling B W; Fong C Y; Alonso M E; Cordova S; Shah P; Khan S; Sainz J; Rubio-Donnadieu F; Sparkes R S
Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
Advances in neurology 1999;79():351-74.
1998: Noble E P; Zhang X; Ritchie T; Lawford B R; Grosser S C; Young R M; Sparkes R S
D2 dopamine receptor and GABA(A) receptor beta3 subunit genes and alcoholism.
Psychiatry research 1998;81(2):133-47.
1998: Noble E P; Ozkaragoz T Z; Ritchie T L; Zhang X; Belin T R; Sparkes R S
D2 and D4 dopamine receptor polymorphisms and personality.
American journal of medical genetics 1998;81(3):257-67.
1997: Sainz J; Minassian B A; Serratosa J M; Gee M N; Sakamoto L M; Iranmanesh R; Bohlega S; Baumann R J; Ryan S; Sparkes R S; Delgado-Escueta A V
Lafora progressive myoclonus epilepsy: narrowing the chromosome 6q24 locus by recombinations and homozygosities.
American journal of human genetics 1997;61(5):1205-9.
1996: Liu A W; Delgado-Escueta A V; Gee M N; Serratosa J M; Zhang Q W; Alonso M E; Medina M T; Cordova S; Zhao H Z; Spellman J M; Donnadieu F R; Peek J R; Treiman L J; Sparkes R S
Juvenile myoclonic epilepsy in chromosome 6p12-p11: locus heterogeneity and recombinations.
American journal of medical genetics 1996;63(3):438-46.
1996: Serratosa J M; Delgado-Escueta A V; Medina M T; Zhang Q; Iranmanesh R; Sparkes R S
Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy.
Annals of neurology 1996;39(2):187-95.
1996: Kojis T L; Heinzmann C; Flodman P; Ngo J T; Sparkes R S; Spence M A; Bateman J B; Heckenlively J R
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.
American journal of human genetics 1996;58(2):347-55.
1995: Serratosa J M; Delgado-Escueta A V; Posada I; Shih S; Drury I; Berciano J; Zabala J A; Antúnez M C; Sparkes R S
The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q.
Human molecular genetics 1995;4(9):1657-63.
1995: McGinnis J F; Austin B; Klisak I; Heinzmann C; Kojis T; Sparkes R S; Bateman J B; Lerious V
Chromosomal assignment of the human gene for the cancer-associated retinopathy protein (recoverin) to chromosome 17p13.1.
Journal of neuroscience research 1995;40(2):165-8.
1994: Noble E P; Syndulko K; Fitch R J; Ritchie T; Bohlman M C; Guth P; Sheridan P J; Montgomery A; Heinzmann C; Sparkes R S
D2 dopamine receptor TaqI A alleles in medically ill alcoholic and nonalcoholic patients.
Alcohol and alcoholism (Oxford, Oxfordshire) 1994;29(6):729-44.
1994: Heinzmann C; Kojis T L; Gonzalez P; Rao P V; Zigler J S; Polymeropoulos M H; Klisak I; Sparkes R S; Mohandas T; Bateman J B
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.
Genomics 1994;23(2):403-7.
1994: Blum M; De Robertis E M; Kojis T; Heinzmann C; Klisak I; Geissert D; Sparkes R S
Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1.
Genomics 1994;21(2):388-93.
1994: Noble E P; Noble R E; Ritchie T; Syndulko K; Bohlman M C; Noble L A; Zhang Y; Sparkes R S; Grandy D K
D2 dopamine receptor gene and obesity.
The International journal of eating disorders 1994;15(3):205-17.
1994: Noble E P; St Jeor S T; Ritchie T; Syndulko K; St Jeor S C; Fitch R J; Brunner R L; Sparkes R S
D2 dopamine receptor gene and cigarette smoking: a reward gene?
Medical hypotheses 1994;42(4):257-60.
1994: Delgado-Escueta A V; Serratosa J M; Liu A; Weissbecker K; Medina M T; Gee M; Treiman L J; Sparkes R S
Progress in mapping human epilepsy genes.
Epilepsia 1994;35 Suppl 1():S29-40.
1993: Ngo J T; Bateman J B; Klisak I; Mohandas T; Van Dop C; Sparkes R S
Regional mapping of a human rod alpha-transducin (GNAT1) gene to chromosome 3p22.
Genomics 1993;18(3):724-5.
1993: Peter D; Finn J P; Klisak I; Liu Y; Kojis T; Heinzmann C; Roghani A; Sparkes R S; Edwards R H
Chromosomal localization of the human vesicular amine transporter genes.
Genomics 1993;18(3):720-3.
1993: Glasgow B J; Heinzmann C; Kojis T; Sparkes R S; Mohandas T; Bateman J B
Assignment of tear lipocalin gene to human chromosome 9q34-9qter.
Current eye research 1993;12(11):1019-23.
1993: Sparkes R S; Lee R H; Shinohara T; Craft C M; Kojis T; Klisak I; Heinzmann C; Bateman J B
Assignment of the phosducin (PDC) gene to human chromosome 1q25-1q32.1 by somatic cell hybridization and in situ hybridization.
Genomics 1993;18(2):426-8.
1993: Warden C H; Mehrabian M; He K Y; Yoon M Y; Diep A; Xia Y R; Wen P Z; Svenson K L; Sparkes R S; Lusis A J
Linkage mapping of 40 randomly isolated liver cDNA clones in the mouse.
Genomics 1993;18(2):295-307.
1993: Cortessis V; Ingles S; Millikan R; Diep A; Gatti R A; Richardson L; Thompson W D; Paganini-Hill A; Sparkes R S; Haile R W
Linkage analysis of DRD2, a marker linked to the ataxia-telangiectasia gene, in 64 families with premenopausal bilateral breast cancer.
Cancer research 1993;53(21):5083-6.
1993: Turk E; Klisak I; Bacallao R; Sparkes R S; Wright E M
Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1.
Genomics 1993;17(3):752-4.
1993: Johnson B; Brooks B A; Heinzmann C; Diep A; Mohandas T; Sparkes R S; Reyes H; Hoffman E; Lange E; Gatti R A
The Ah receptor nuclear translocator gene (ARNT) is located on q21 of human chromosome 1 and on mouse chromosome 3 near Cf-3.
Genomics 1993;17(3):592-8.
1993: Bateman J B; Kojis T; Heinzmann C; Klisak I; Diep A; Carper D; Nishimura C; Mohandas T; Sparkes R S
Mapping of aldose reductase gene sequences to human chromosomes 1, 3, 7, 9, 11, and 13.
Genomics 1993;17(3):560-5.
1993: Xia Y R; Klisak I; Sparkes R S; Oram J; Lusis A J
Localization of the gene for high-density lipoprotein binding protein (HDLBP) to human chromosome 2q37.
Genomics 1993;16(2):524-5.
1993: Aurer I; Sparkes R S; Schiller G; Gale R P
Ph1-chromosome positive acute lymphoblastic leukemia: is t(9;22) the initial abnormality?
American journal of hematology 1993;43(1):61-2.
1993: Shieh B H; Sparkes R S; Gaynor R B; Lusis A J
Localization of the gene-encoding upstream stimulatory factor (USF) to human chromosome 1q22-q23.
Genomics 1993;16(1):266-8.
1993: Mehrabian M; Gitt M A; Sparkes R S; Leffler H; Barondes S H; Lusis A J
Two members of the S-lac lectin gene family, LGALS1 and LGALS2, reside in close proximity on human chromosome 22q12-q13.
Genomics 1993;15(2):418-20.
1993: Tsukada S; Saffran D C; Rawlings D J; Parolini O; Allen R C; Klisak I; Sparkes R S; Kubagawa H; Mohandas T; Quan S
Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia.
Cell 1993;72(2):279-90.
1993: Haile R W; Cortessis V K; Millikan R; Ingles S; Aragaki C C; Richardson L; Thompson W D; Paganini-Hill A; Sparkes R S
A linkage analysis of D17S74 (CMM86) in thirty-five families with premenopausal bilateral breast cancer.
Cancer research 1993;53(2):212-4.
1993: Gaynor R B; Shieh B H; Klisak I; Sparkes R S; Lusis A J
Localization of the transcription factor SP1 gene to human chromosome 12q12-->q13.2.
Cytogenetics and cell genetics 1993;64(3-4):210-2.
1993: Bateman J B; Kojis T L; Cantor R M; Heinzmann C; Ngo J T; Spence M A; Inana G; Kivlin J D; Curtis D; Sparkes R S
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.
Transactions of the American Ophthalmological Society 1993;91():299-307; discussion 307-8.
1992: MacLaren D C; O'Connor C M; Xia Y R; Mehrabian M; Klisak I; Sparkes R S; Clarke S; Lusis A J
The L-isoaspartyl/D-aspartyl protein methyltransferase gene (PCMT1) maps to human chromosome 6q22.3-6q24 and the syntenic region of mouse chromosome 10.
Genomics 1992;14(4):852-6.
1992: Garcia J A; Ou S H; Wu F; Lusis A J; Sparkes R S; Gaynor R B
Cloning and chromosomal mapping of a human immunodeficiency virus 1 "TATA" element modulatory factor.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(20):9372-6.
1992: Li C; Lusis A J; Sparkes R; Tran S M; Gaynor R
Characterization and chromosomal mapping of the gene encoding the cellular DNA binding protein HTLF.
Genomics 1992;13(3):658-64.
1992: Li C; Lusis A J; Sparkes R; Nirula A; Gaynor R
Characterization and chromosomal mapping of the gene encoding the cellular DNA binding protein ILF.
Genomics 1992;13(3):665-71.
1992: Shieh B H; Xia Y; Sparkes R S; Klisak I; Lusis A J; Nicoll D A; Philipson K D
Mapping of the gene for the cardiac sarcolemmal Na(+)-Ca2+ exchanger to human chromosome 2p21-p23.
Genomics 1992;12(3):616-7.
1992: Bateman J B; Klisak I; Kojis T; Mohandas T; Sparkes R S; Li T S; Applebury M L; Bowes C; Farber D B
Assignment of the beta-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse rd gene) to human chromosome 4p16.
Genomics 1992;12(3):601-3.
1992: Sparkes R S; Heinzmann C; Goldflam S; Kojis T; Saari J C; Mohandas T; Klisak I; Bateman J B; Crabb J W
Assignment of the gene (RLBP1) for cellular retinaldehyde-binding protein (CRALBP) to human chromosome 15q26 and mouse chromosome 7.
Genomics 1992;12(1):58-62.
1992: Lindsay S; Thiselton D L; Bateman J B; Ngo J T; Sparkes R S; Coleman M; Davies K E; Bhattacharya S S
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.
Human genetics 1992;88(3):349-50.
1991: Diep A; Li C; Klisak I; Mohandas T; Sparkes R S; Gaynor R; Lusis A J
Assignment of the gene for cyclic AMP-response element binding protein 2 (CREB2) to human chromosome 2q24.1-q32.
Genomics 1991;11(4):1161-3.
1991: Davis R C; Diep A; Hunziker W; Klisak I; Mohandas T; Schotz M C; Sparkes R S; Lusis A J
Assignment of human pancreatic lipase gene (PNLIP) to chromosome 10q24-q26.
Genomics 1991;11(4):1164-6.
1991: Farber D B; Heckenlively J R; Sparkes R S; Bateman J B
Molecular genetics of retinitis pigmentosa.
The Western journal of medicine 1991;155(4):388-99.
1991: Kojis T L; Heinzmann C; Travis G H; Bateman J B; Sparkes R S
Three polymorphisms detected by a retinal degeneration slow (rds) probe (RDS).
Nucleic acids research 1991;19(19):5446.
1991: Gaynor R B; Muchardt C; Xia Y R; Klisak I; Mohandas T; Sparkes R S; Lusis A J
Localization of the gene for the DNA-binding protein AP-2 to human chromosome 6p22.3-pter.
Genomics 1991;10(4):1100-2.
1991: Sparkes R S; Klisak I; Miller W L
Regional mapping of genes encoding human steroidogenic enzymes: P450scc to 15q23-q24, adrenodoxin to 11q22; adrenodoxin reductase to 17q24-q25; and P450c17 to 10q24-q25.
DNA and cell biology 1991;10(5):359-65.
1991: Taylor A K; Zambaux J L; Klisak I; Mohandas T; Sparkes R S; Schotz M C; Lusis A J
Carboxyl ester lipase: a highly polymorphic locus on human chromosome 9qter.
Genomics 1991;10(2):425-31.
1991: Gaynor R B; Muchardt C; Diep A; Mohandas T K; Sparkes R S; Lusis A J
Localization of the zinc finger DNA-binding protein HIV-EP1/MBP-1/PRDII-BF1 to human chromosome 6p22.3-p24.
Genomics 1991;9(4):758-61.
1991: Sparkes R S; Lan N; Klisak I; Mohandas T; Diep A; Kojis T; Heinzmann C; Shih J C
Assignment of a serotonin 5HT-2 receptor gene (HTR2) to human chromosome 13q14-q21 and mouse chromosome 14.
Genomics 1991;9(3):461-5.
1991: Gatti R A; Boder E; Vinters H V; Sparkes R S; Norman A; Lange K
Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis.
Medicine 1991;70(2):99-117.
1991: Mehrabian M; Sparkes R S; Mohandas T; Fogelman A M; Lusis A J
Localization of monocyte chemotactic protein-1 gene (SCYA2) to human chromosome 17q11.2-q21.1.
Genomics 1991;9(1):200-3.
1991: Sun G; Wormsley S; Sparkes R S; Naeim F; Gale R P
Hybrid leukemia and the 5q-abnormality.
Leukemia research 1991;15(5):351-6.
1991: Delgado-Escueta A V; Greenberg D A; Weissbecker K; Serratosa J M; Liu A; Treiman L J; Sparkes R; Park M S; Barbetti A
The choice of epilepsy syndromes for genetic analysis.
Epilepsy research. Supplement 1991;4():147-59.
1991: Sun G X; Wormsley S; Sparkes R S; Naeim F; Gale R P
Where does transformation occur in acute leukemia?
Leukemia research 1991;15(12):1183-9.
1990: Lusis A J; Rajavashisth T B; Klisak I; Heinzmann C; Mohandas T; Sparkes R S
Mapping of the gene for CNBP, a finger protein, to human chromosome 3q13.3-q24.
Genomics 1990;8(2):411-4.
1990: Sun G X; Sparkes R S; Wormsley S; Naeim F; Champlin R; Gale R P
Are some cases of acute leukemia with t(8;21) hybrid leukemias?
Cancer genetics and cytogenetics 1990;49(2):177-84.
1990: Taylor A K; Klisak I; Mohandas T; Sparkes R S; Li C; Gaynor R; Lusis A J
Assignment of the human gene for CREB1 to chromosome 2q32.3-q34.
Genomics 1990;7(3):416-21.
1990: Ngo J T; Klisak I; Sparkes R S; Mohandas T; Yamaki K; Shinohara T; Bateman J B
Assignment of the S-antigen gene (SAG) to human chromosome 2q24-q37.
Genomics 1990;7(1):84-7.
1990: Sun G X; Koeffler H P; Gale R P; Sparkes R S; Schreck R R
Use of conditioned media in cell culture can mask cytogenetic abnormalities in acute leukemia.
Cancer genetics and cytogenetics 1990;46(1):107-13.
1990: Forrest G L; Akman S; Krutzik S; Paxton R J; Sparkes R S; Doroshow J; Felsted R L; Glover C J; Mohandas T; Bachur N R
Induction of a human carbonyl reductase gene located on chromosome 21.
Biochimica et biophysica acta 1990;1048(2-3):149-55.
1990: Tuteja N; Danciger M; Klisak I; Tuteja R; Inana G; Mohandas T; Sparkes R S; Farber D B
Isolation and characterization of cDNA encoding the gamma-subunit of cGMP phosphodiesterase in human retina.
Gene 1990;88(2):227-32.
1990: Ngo J T; Bateman J B; Spence M A; Cortessis V; Sparkes R S; Kivlin J D; Mohandas T; Inana G
Ornithine aminotransferase (OAT): recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locus.
Genomics 1990;6(1):123-8.
1990: Delgado-Escueta A V; Greenberg D; Weissbecker K; Liu A; Treiman L; Sparkes R; Park M S; Barbetti A; Terasaki P I
Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy.
Epilepsia 1990;31 Suppl 3():S19-29.
1989: Lau Y F; Chan K M; Sparkes R
Male-enhanced antigen gene is phylogenetically conserved and expressed at late stages of spermatogenesis.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(21):8462-6.
1989: Ngo J T; Klisak I; Dubin R A; Piatigorsky J; Mohandas T; Sparkes R S; Bateman J B
Assignment of the alpha B-crystallin gene to human chromosome 11.
Genomics 1989;5(4):665-9.
1989: Heinzmann C; Clarke C F; Klisak I; Mohandas T; Sparkes R S; Edwards P A; Lusis A J
Dispersed family of human genes with sequence similarity to farnesyl pyrophosphate synthetase.
Genomics 1989;5(3):493-500.
1989: Sparkes R S; Kronenberg M; Heinzmann C; Daher K A; Klisak I; Ganz T; Mohandas T
Assignment of defensin gene(s) to human chromosome 8p23.
Genomics 1989;5(2):240-4.
1989: Goldstein A M; Haile R W; Spence M A; Sparkes R S; Paganini-Hill A
A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. II. Linkage analysis.
Clinical genetics 1989;36(2):100-6.
1989: Ngo J; Spence M A; Cortessis V; Bateman J B; Sparkes R S
Duplicate report crossing over in Norrie disease family.
American journal of medical genetics 1989;33(2):286.
1989: Ngo J T; Bateman J B; Cortessis V; Sparkes R S; Mohandas T; Inana G; Spence M A
Norrie disease: linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe.
Genomics 1989;4(4):539-45.
1989: Frank S L; Klisak I; Sparkes R S; Lusis A J
A gene homologous to plasminogen located on human chromosome 2q11-p11.
Genomics 1989;4(3):449-51.
1989: Sparkes R S
Human gene mapping and linkage analysis.
Immunology series 1989;43():33-52.
1989: Delgado-Escueta A V; Greenberg D A; Treiman L; Liu A; Sparkes R S; Barbetti A; Park M S; Terasaki P I
Mapping the gene for juvenile myoclonic epilepsy.
Epilepsia 1989;30 Suppl 4():S8-18; discussion S24-7.
1988: Greenberg D A; Delgado-Escueta A V; Widelitz H; Sparkes R S; Treiman L; Maldonado H M; Park M S; Terasaki P I
Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6.
American journal of medical genetics 1988;31(1):185-92.
1988: Frank S L; Klisak I; Sparkes R S; Mohandas T; Tomlinson J E; McLean J W; Lawn R M; Lusis A J
The apolipoprotein(a) gene resides on human chromosome 6q26-27, in close proximity to the homologous gene for plasminogen.
Human genetics 1988;79(4):352-6.
1988: Ngo J T; Spence M A; Cortessis V; Sparkes R S; Bateman J B
Recombinational event between Norrie disease and DXS7 loci.
Clinical genetics 1988;34(1):43-7.
1988: Barrett D J; Sparkes R S; Gorin M B; Bhat S P; Spence M A; Marazita M L; Bateman J B
Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markers.
Ophthalmology 1988;95(4):538-44.
1988: Chen S A; Besman M J; Sparkes R S; Zollman S; Klisak I; Mohandas T; Hall P F; Shively J E
Human aromatase: cDNA cloning, Southern blot analysis, and assignment of the gene to chromosome 15.
DNA (Mary Ann Liebert, Inc.) 1988;7(1):27-38.
1988: Dreazen O; Klisak I; Rassool F; Goldman J M; Sparkes R S; Gale R P
The bcr gene is joined to c-abl in Ph1 chromosome negative chronic myelogenous leukemia.
Oncogene research 1988;2(2):167-75.
1987: Kosmo M A; Mitsuyasu R T; Sparkes R S; Gale R P
Trisomy 12 in Burkitt-like lymphoma associated with acquired immunodeficiency syndrome.
Cancer genetics and cytogenetics 1987;29(2):245-51.
1987: Gatti R A; Davis R C; Weeks D E; Jaspers N J; Sparkes R S; Lange K
Genetic linkage studies of ataxia-telangiectasia: phenotypic blood markers.
Disease markers 1987;5(4):207-13.
1987: Dreazen O; Klisak I; Jones G; Ho W G; Sparkes R S; Gale R P
Multiple molecular abnormalities in Ph1 chromosome positive acute lymphoblastic leukaemia.
British journal of haematology 1987;67(3):319-24.
1987: Lusis A J; Zollman S; Sparkes R S; Klisak I; Mohandas T; Drayna D; Lawn R M
Assignment of the human gene for cholesteryl ester transfer protein to chromosome 16q12-16q21.
Genomics 1987;1(3):232-5.
1987: Hogg D; Gorin M B; Heinzmann C; Zollman S; Mohandas T; Klisak I; Sparkes R S; Breitman M; Tsui L C; Horwitz J
Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22.
Current eye research 1987;6(11):1335-42.
1987: Sweetser D A; Birkenmeier E H; Klisak I J; Zollman S; Sparkes R S; Mohandas T; Lusis A J; Gordon J I
The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships.
The Journal of biological chemistry 1987;262(33):16060-71.
1987: Sparkes R S; Zollman S; Klisak I; Kirchgessner T G; Komaromy M C; Mohandas T; Schotz M C; Lusis A J
Human genes involved in lipolysis of plasma lipoproteins: mapping of loci for lipoprotein lipase to 8p22 and hepatic lipase to 15q21.
Genomics 1987;1(2):138-44.
1987: Spence M A; Sparkes R S; Parry D M; Bale S J; Cortessis V; Mulvihill J J
Genetic linkage studies with neurofibromatosis: the question of heterogeneity.
Journal of medical genetics 1987;24(9):527-9.
1987: Barrett D J; Bateman J B; Sparkes R S; Mohandas T; Klisak I; Inana G
Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.
Investigative ophthalmology & visual science 1987;28(7):1037-42.
1987: Stathacopoulos R A; Bateman J B; Sparkes R S; Hepler R S
The Rieger syndrome and a chromosome 13 deletion.
Journal of pediatric ophthalmology and strabismus 1987;24(4):198-203.
1987: Dreazen O; Klisak I; Rassool F; Goldman J M; Sparkes R S; Gale R P
Do oncogenes determine clinical features in chronic myeloid leukaemia?
Lancet 1987;1(8547):1402-5.
1987: Demmer L A; Birkenmeier E H; Sweetser D A; Levin M S; Zollman S; Sparkes R S; Mohandas T; Lusis A J; Gordon J I
The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding protein gene.
The Journal of biological chemistry 1987;262(6):2458-67.
1986: Sparkes R S; Mohandas T; Heinzmann C; Gorin M B; Zollman S; Horwitz J
Assignment of a human beta-crystallin gene to 17cen-q23.
Human genetics 1986;74(2):133-6.
1986: Sparkes R S; Mohandas T; Heinzmann C; Gorin M B; Horwitz J; Law M L; Jones C A; Bateman J B
The gene for the major intrinsic protein (MIP) of the ocular lens is assigned to human chromosome 12cen-q14.
Investigative ophthalmology & visual science 1986;27(9):1351-4.
1986: Sparkes R S; Dizikes G J; Klisak I; Grody W W; Mohandas T; Heinzmann C; Zollman S; Lusis A J; Cederbaum S D
The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23.
American journal of human genetics 1986;39(2):186-93.
1986: Sparkes R S; Mohandas T; Newman S L; Heinzmann C; Kaufman D; Zollman S; Leveille P J; Tobin A J; McGinnis J F
Assignment of the rhodopsin gene to human chromosome 3.
Investigative ophthalmology & visual science 1986;27(7):1170-2.
1986: Mehrabian M; Sparkes R S; Mohandas T; Klisak I J; Schumaker V N; Heinzmann C; Zollman S; Ma Y H; Lusis A J
Human apolipoprotein B: chromosomal mapping and DNA polymorphisms of hepatic and intestinal species.
Somatic cell and molecular genetics 1986;12(3):245-54.

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