Lowell Weitkamp
| Title | Professor Emeritus |
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| Institution | School of Medicine and Dentistry |
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| Department | Psychiatry |
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| Address | 150 Jeffords Road
Rush NY 14543
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Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR, Rodier PM. Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders. Teratology. 2000 Dec; 62(6):393-405.
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Génin E, Ober C, Weitkamp L, Thomson G. A robust test for assortative mating. Eur J Hum Genet. 2000 Feb; 8(2):119-24.
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Weitkamp LR, Ober C. Ancestral and recombinant 16-locus HLA haplotypes in the Hutterites. Immunogenetics. 1999 Jun; 49(6):491-7.
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Weitkamp LR, Tackels DC, Hunter AG, Holmes LB, Schwartz CE. Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives. Lancet. 1998 May 23; 351(9115):1554-5.
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Ober C, Hyslop T, Elias S, Weitkamp LR, Hauck WW. Human leukocyte antigen matching and fetal loss: results of a 10 year prospective study. Hum Reprod. 1998 Jan; 13(1):33-8.
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Ober C, Weitkamp LR, Cox N, Dytch H, Kostyu D, Elias S. HLA and mate choice in humans. Am J Hum Genet. 1997 Sep; 61(3):497-504.
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Forbes GB, Sauer EP, Weitkamp LR. Lean body mass in twins. Metabolism. 1995 Nov; 44(11):1442-6.
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Weitkamp LR, Moss AJ, Lewis RA, Hall WJ, MacCluer JW, Schwartz PJ, Locati EH, Tzivoni D, Vincent GM, Robinson JL, et al. Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype. Am J Hum Genet. 1994 Dec; 55(6):1230-41.
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Schiffer RB, Weitkamp LR, Ford C, Hall WJ. A genetic marker and family history study of the upstate New York multiple sclerosis cluster. Neurology. 1994 Feb; 44(2):329-33.
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Weitkamp LR, Lewis RA. PEDSCORE analysis of identical by descent (IBD) marker allele distributions among family members with cutaneous melanoma. Cytogenet Cell Genet. 1992; 59(2-3):231-3.
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VandeBerg JL, Weitkamp L, Kammerer CM, Weill P, Aivaliotis MJ, Rainwater DL. Linkage of plasminogen (PLG) and apolipoprotein(a) (LPA) in baboons. Genomics. 1991 Dec; 11(4):925-30.
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Moss AJ, Schwartz PJ, Crampton RS, Tzivoni D, Locati EH, MacCluer J, Hall WJ, Weitkamp L, Vincent GM, Garson A, et al. The long QT syndrome. Prospective longitudinal study of 328 families. Circulation. 1991 Sep; 84(3):1136-44.
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Weitkamp LR, Kenney RM, Bailey E, MacCluer JW, Brown JS, Blanchard TL, Sertich PL, Love CC, Hunt PR. Pathological changes of the mare endometrium and genotypes for transferrin and ELA. J Reprod Fertil Suppl. 1991; 44:275-82.
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Stancer HC, Weitkamp LR, Persad E, Flood C, Jorna T, Guttormsen SA, Yagnow RL. Toronto-Rochester Depression study of 116 HLA-typed kindreds. Genet Epidemiol. 1989; 6(1):191-4.
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Weitkamp LR, Stancer HC. Analysis of the Toronto-Rochester Depression Study follow-up data confirms an HLA-region gene contribution to susceptibility to affective disorder. Genet Epidemiol. 1989; 6(1):305-10.
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Schiffer RB, Weitkamp LR, Wineman NM, Guttormsen S. Multiple sclerosis and affective disorder. Family history, sex, and HLA-DR antigens. Arch Neurol. 1988 Dec; 45(12):1345-8.
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Stancer HC, Weitkamp LR, Persad E, Flood C, Jorna T, Guttormsen SA, Yagnow RL. Confirmation of the relationship of HLA (chromosome 6) genes to depression and manic depression. II. The Ontario follow-up and analysis of 117 kindreds. Ann Hum Genet. 1988 Oct; 52(Pt 4):279-98.
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Weitkamp LR, Guttormsen SA, Schultz JS. Linkage between the loci for the Lp(a) lipoprotein (LP) and plasminogen (PLG). Hum Genet. 1988 May; 79(1):80-2.
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Forbes GB, Prochaska E, Weitkamp LR. Genetic factors in abdominal obesity, a risk factor for stroke. N Engl J Med. 1988 Apr 21; 318(16):1070.
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Weitkamp LR, MacCluer JW, Guttormsen SA, King RH. Standardbred stallion gene transmission for twelve protein systems: evidence for selection in trotters. Anim Genet. 1988; 19(4):317-30.
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Juneja RK, Weitkamp LR, Stratil A, Gahne B, Guttormsen SA. Further studies of the plasma alpha 1 B-glycoprotein polymorphism: two new alleles and allele frequencies in Caucasians and in American blacks. Hum Hered. 1988; 38(5):267-72.
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MacCluer JW, Bailey E, Weitkamp LR, Blangero J. ELA and fertility in American Standardbred horses. Anim Genet. 1988; 19(4):359-72.
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Stancer HC, Mellor C, Weitkamp LR, Jorna T, Flood C, Persad E, Jain SC, Guttormsen S. The relationship of HLA to depression and manic depression. I. The Newfoundland follow-up. Can J Psychiatry. 1987 Dec; 32(9):768-72.
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Cothran EG, MacCluer JW, Weitkamp LR, Bailey E. Genetic differentiation associated with gait within American standardbred horses. Anim Genet. 1987; 18(4):285-96.
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Rich SS, Weitkamp LR, Guttormsen S, Barbosa J. Gm, Km, and HLA in insulin-dependent type I diabetes mellitus. A log-linear analysis of association. Diabetes. 1986 Aug; 35(8):927-32.
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Boughman JA, Halloran SL, Roulston D, Schwartz S, Suzuki JB, Weitkamp LR, Wenk RE, Wooten R, Cohen MM. An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc. J Craniofac Genet Dev Biol. 1986; 6(4):341-50.
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Schiffer RB, Wineman NM, Weitkamp LR. Association between bipolar affective disorder and multiple sclerosis. Am J Psychiatry. 1986 Jan; 143(1):94-5.
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Weitkamp LR, Schacter BZ. Transferrin and HLA: spontaneous abortion, neural tube defects, and natural selection. N Engl J Med. 1985 Oct 10; 313(15):925-32.
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Caine ED, Weitkamp LR, Chiverton P, Guttormsen S, Yagnow R, Hempfling S, Kennelly D. Tourette syndrome and HLA. J Neurol Sci. 1985 Jul; 69(3):201-6.
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Weitkamp LR, Bailey E. Genetic linkage relationships of equine plasminogen (PLG) with 23 loci. Anim Blood Groups Biochem Genet. 1985; 16(1):61-3.
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Haines JL, Schut LJ, Weitkamp LR, Thayer M, Anderson VE. Spinocerebellar ataxia in a large kindred: age at onset, reproduction, and genetic linkage studies. Neurology. 1984 Dec; 34(12):1542-8.
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Rich SS, Weitkamp LR, Barbosa J. Genetic heterogeneity of insulin-dependent (type I) diabetes mellitus: evidence from a study of extended haplotypes. Am J Hum Genet. 1984 Sep; 36(5):1015-23.
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Schacter B, Weitkamp LR, Johnson WE. Parental HLA compatibility, fetal wastage and neural tube defects: evidence for a T/t-like locus in humans. Am J Hum Genet. 1984 Sep; 36(5):1082-91.
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Cothran EG, MacCluer JW, Weitkamp LR, Pfennig DW, Boyce AJ. Inbreeding and reproductive performance in standardbred horses. J Hered. 1984 May-Jun; 75(3):220-4.
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Weitkamp LR. Evidence for linkage between the loci for transferrin and ceruloplasmin in man. Ann Hum Genet. 1983 Oct; 47(Pt 4):293-7.
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Khan MA, Kushner I, Weitkamp LR. Genetics of HLA-associated disease; rheumatoid arthritis. Tissue Antigens. 1983 Sep; 22(3):182-5.
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Weitkamp LR. Multiple sclerosis susceptibility. Interaction between sex and HLA. Arch Neurol. 1983 Jul; 40(7):399-401.
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Weitkamp LR, Nee L, Keats B, Polinsky RJ, Guttormsen S. Alzheimer disease: evidence for susceptibility loci on chromosomes 6 and 14. Am J Hum Genet. 1983 May; 35(3):443-53.
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Weitkamp LR, Costello-Leary P, Guttormsen SA. Equine marker genes: polymorphism for plasminogen. Anim Blood Groups Biochem Genet. 1983; 14(3):219-23.
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Weitkamp LR. Genetic analysis of multifactorial diseases. Am J Hum Genet. 1983 Jan; 35(1):130-3.
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Weitkamp LR, Lamm LU. Report of the committee on the genetic constitution of chromosome 6. Birth Defects Orig Artic Ser. 1982; 18(2):130-43.
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Weitkamp LR, Lamm LU. Report of the committee on the genetic constitution of chromosome 6. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet Cell Genet. 1982; 32(1-4):130-43.
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Weitkamp LR, Guttormsen SA, Costello-Leary P. Equine gene mapping: a sex difference in recombination frequency for linkage group II. Anim Blood Groups Biochem Genet. 1982; 13(4):305-6.
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Weitkamp LR, MacCluer JW, Guttormsen S, McKnight J, Wert N, Witmer J, Boyce P, Egloff J. Genetics of Standardbred stallion reproductive performance. J Reprod Fertil Suppl. 1982; 32:135-42.
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Weitkamp LR, Berg K, Gedde-Dahl T, Hulten MA, McAlpine PJ, Sandberg K, Spence MA. Workshop on mapping by classical methods. Prog Clin Biol Res. 1982; 103 Pt A:141-4.
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Weitkamp LR, Guttormsen SA, Costello-Leary P. Equine gene mapping: close linkage between the loci for soluble malic enzyme and Xk (Pa). Anim Blood Groups Biochem Genet. 1982; 13(4):279-84.
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Weitkamp LR, Stancer HC, Persad E, Flood C, Guttormsen S. Depressive disorders and HLA: a gene on chromosome 6 that can affect behavior. N Engl J Med. 1981 Nov 26; 305(22):1301-6.
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Weitkamp LR. HLA and disease: predictions for HLA haplotype sharing in families. Am J Hum Genet. 1981 Sep; 33(5):776-84.
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Ichikawa K, Crosley CJ, Culebras A, Weitkamp L. Coincidence of neurofibromatosis and myotonic dystrophy in a kindred. J Med Genet. 1981 Apr; 18(2):134-8.
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Goudsmit J, White BJ, Weitkamp LR, Keats BJ, Morrow CH, Gajdusek DC. Familial Alzheimer's disease in two kindreds of the same geographic and ethnic origin. A clinical and genetic study. J Neurol Sci. 1981 Jan; 49(1):79-89.
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Guttormsen SA, Weitkamp LR. Equine marker genes: Polymorphism for soluble erythrocyte malic enzyme. Anim Blood Groups Biochem Genet. 1981; 12(1):53-7.
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Weitkamp LR, Pardue LH, Huntzinger RS. Genetic marker studies in a family with unipolar depression. Arch Gen Psychiatry. 1980 Oct; 37(10):1187-92.
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Francke U, Weitkamp LR. Report of the committee on the genetic constitution of chromosome 6. Birth Defects Orig Artic Ser. 1980; 15(11):32-8.
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McGuire TR, Weitkamp LR. Equine marker genes. Polymorphism for transferrin alleles, TfF1 and TfF2, in Thoroughbreds. Anim Blood Groups Biochem Genet. 1980; 11(2):113-7.
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Barbosa J, Weitkamp L, Guttormsen S, Johnson S, Szalapski E. Bf in early-onset insulin-dependent diabetes. Lancet. 1979 Dec 8; 2(8154):1239-40.
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Weitkamp LR. HLA segregation ratios. Lancet. 1979 Oct 6; 2(8145):745.
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Yut J, Weitkamp LR. Equine peptidases: correspondence with human peptidases and polymorphism for erythrocyte peptidase A. Biochem Genet. 1979 Oct; 17(9-10):987-94.
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Weitkamp LR, Barbosa J, Guttormsen SA, Johnson S. Insulin-dependent diabetes mellitus and properdin factor B. Lancet. 1979 Aug 18; 2(8138):369-70.
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Weitkamp LR, Allen PZ. Evolutionary conservation of equine gc alleles and of Mammalian gc/albumin linkage. Genetics. 1979 Aug; 92(4):1347-54.
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Francke U, Weitkamp LR. Report of the committee on the genetic constitution of chromosome 6. Cytogenet Cell Genet. 1979; 25(1-4):32-8.
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Rosenfeld SI, Weitkamp LR, Countryman JK. Linkage for a locus of human complement C5 deficiency to the complement C6 structural locus. Immunogenetics. 1978 Dec; 7(1):95-7.
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Weitkamp LR, Ferguson-Smith MA, Guttormsen SA, Huntzinger RS, Chaganti RS, German J, Schanfield MS. The linkage relationships of marker sites on chromosomes no. 2 and 10. Ann Hum Genet. 1978 Oct; 42(2):183-9.
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Weitkamp LR. Concerning the linkage relationships of the Gc and MNSs loci. Hum Genet. 1978 Aug 31; 43(2):215-20.
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Huntzinger RS, Weitkamp LR, Roca PD. Linkage relations of a locus for congenital total nuclear cataract. J Med Genet. 1978 Apr; 15(2):113-5.
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Lamm LU, Weitkamp LR, Jensson O, Pedersen GB, Kissmeyer-Nielsen F. On the mapping of PGM3, GLO and HLA. Tissue Antigens. 1978 Feb; 11(2):132-8.
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Weitkamp LR. Further data concerning the linkage relationships of loci for urinary pepsinogen and HLA. Cytogenet Cell Genet. 1978; 22(1-6):341-5.
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Weitkamp LR, Rosenfeld S, Johnston E. Complement C5: immunofixation electrophoresis, quantitative variants, and nonlinkage to HLA. Cytogenet Cell Genet. 1978; 22(1-6):651-4.
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Weitkamp LR. Equine markers genes. Polymorphism for group-specific component (Gc). Anim Blood Groups Biochem Genet. 1978; 9(2):123-6.
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Weitkamp LR, Cox D, Guttormsen S, Johnston E, Hempfling S. Allelic specific heterogeneity in the Pi:Gm linkage group. Cytogenet Cell Genet. 1978; 22(1-6):647-50.
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Rosenfeld SI, Weitkamp LR, Ward F. Hereditary C5 deficiency in man: genetic linkage studies. J Immunol. 1977 Aug; 119(2):604-8.
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Weitkamp LR, Stamatoyannopoulos G, Rowley PT, Kirk RL. The linkage relationships of the haemoglobin beta, delta and alpha loci with 34 genetic marker systems. Ann Hum Genet. 1977 Jul; 41(1):61-75.
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Stamatoyannopoulos G, Weitkamp LR, Kotsakis P, Akrivakis A. The linkage relationships of the beta and delta hemoglobin genes. Hemoglobin. 1977; 1(6):561-70.
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Weitkamp LR. Linkage of GLO with HLA and Bf. Effect of population and sex on recombination frequency. Tissue Antigens. 1976 May; 7(5):273-9.
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Basu A, Namboodiri KK, Weitkamp LR, Brown WH, Pollitzer WS, Spivey MA. Morphology, serology, dermatoglyphics, and microevolution of some village populations in Haiti, West Indies. Hum Biol. 1976 May; 48(2):245-69.
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Weitkamp LR, Sayre JW, Schwartz RH, Doherty R, Khera SA. 'Durate variant with clinical signs' has alpha1 -antitrypsin genotype ZZ. J Med Genet. 1976 Feb; 13(1):46-8.
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Weitkamp LR, Schwartz RH, Cox D. Possible association between the Duarte gene of galactose-1-phosphate uridyl transferase and the ZZ or SZ genotype of alpha1-antitrypsin. Birth Defects Orig Artic Ser. 1976; 12(6):309-11.
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Weitkamp LR, Cox DW, Johnston E, Guttormsen SA, Schwartz RH, Bias WB, Hsu SH. Data on the genetic linkage relationships between red cell acid phosphatase and alpha1-antitrypsin variants Z, S, I, and F. Cytogenet Cell Genet. 1976; 16(1-5):359-63.
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Weitkamp LR, Guttormsen SA. Genetic linkage of a locus for erythrocyte glyoxalase (GLO) with HLA and Bf. Cytogenet Cell Genet. 1976; 16(1-5):364-6.
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Edwards JH, Weitkamp LR. Report of the committee on unassigned linkage groups. Birth Defects Orig Artic Ser. 1976; 12(7):60-4.
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Weitkamp LR, Guttormsen SA. Genetic linkage of a locus for erythrocyte glyoxalase (GLO) with HLA and Bf. Birth Defects Orig Artic Ser. 1976; 12(7):364-6.
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Weitkamp LR, Cox DW, Jhnston E, Guttormsen SA, Schwartz RH, Bias WB, Hsu SH. Data on the genetic linkage relationships between red cell acid phosphatase and alpha1-antitrypsin variants Z, S, I, and F. Birth Defects Orig Artic Ser. 1976; 12(7):359-63.
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Weitkamp LR, Townes PL, May AG. Probable genetic linkage between a locus for human urinary pepsinogen and the HL-A loci. Am J Hum Genet. 1975 Jul; 27(4):486-91.
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Weitkamp LR, Townes PL, Johnston E. Linkage data on urinary pepsinogen and the Kell blood group. Cytogenet Cell Genet. 1975; 14(3-6):451-2.
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Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T, Sorensen SA, Conneally PM, Bias WB, Ott J. Linkage relations of the loci for the MN blood group and red cell acid phosphatase. Birth Defects Orig Artic Ser. 1975; 11(3):276-80.
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Weitkamp LR, Townes PL, Johnston E. Linkage data on urinary pepsinogen and the Kell blood group. Birth Defects Orig Artic Ser. 1975; 11(3):281-2.
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Chaganti RS, Weitkamp LR, Fleming J, Miller G, German J. Polymorphic chromosomes and gene assignment in man. Birth Defects Orig Artic Ser. 1975; 11(3):93-8.
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Weitkamp LR, May AG, Johnston E. The linkage relationships of HL-A with other genetic marker systems. Hum Hered. 1975; 25(5):337-45.
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Weitkamp LR, Lovrien EW, Olaisen B, Fenger K, Gedde-Dahl T, Sorensen SA, Conneally PM, Bias WB, Ott J. Linkage relations of the loci for the MN blood group and red cell acid phosphatase. Cytogenet Cell Genet. 1975; 14(3-6):446-50.
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Chaganti RS, Weitkamp LR, Fleming J, Miller G, German J. Polymorphic chromosomes and gene assignment in man. Cytogenet Cell Genet. 1975; 14(3-6):263-8.
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MacLean CH, Adams MS, Leyshon WC, Workman PL, Reed TE, Gershowitz H, Weitkamp LR. Genetic studies on hybrid populations. 3. Blood pressure in an American black community. Am J Hum Genet. 1974 Sep; 26(5):614-26.
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Weitkamp LR, Yamamoto M, Nishiyama J. The population distribution of uncommon, inherited albumin variants: two examples from Japan. Ann Hum Genet. 1974 May; 37(4):485-8.
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Salzano FM, Woodall JP, Black FL, Weitkamp LR, Franco MH. Blood groups, serum proteins and hemoglobins of Brazilian Tiriyo Indians. Hum Biol. 1974 Feb; 46(1):81-7.
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Weitkamp LR. Proceedings: Population differences in meiotic recombination frequency between loci on chromosome 1. Cytogenet Cell Genet. 1974; 13(1):179-82.
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Weitkamp LR, Johnston E, Guttormsen SA. Proceedings: Probable genetic linkage between the loci for the Lewis blood group and complement C3. Cytogenet Cell Genet. 1974; 13(1):183-4.
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Weitkamp LR, McDermid EM, Neel JV, Fine JM, Petrini C, Bonazzi L, Ortali V, Porta F, Tanis R, Harris DJ, Peters T, Ruffini G, Johnston E. Additional data on the population distribution of human serum albumin genes; three new variants. Ann Hum Genet. 1973 Oct; 37(2):219-26.
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Weitkamp LR. The contribution of variations in serum albumin to the characterization of human populations. Isr J Med Sci. 1973 Sep-Oct; 9(9):1238-48.
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Weitkamp LR, Salzano FM, Neel JV, Porta F, Geerdink RA, Tárnoky AL. Human serum albumin: twenty-three genetic variants and their population distribution. Ann Hum Genet. 1973 Apr; 36(4):381-92.
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Weitkamp LR, Van Rood JJ, Thorsby E, Bias W, Fotino M, Lawler SD, Dausset J, Mayr WR, Bodmer J, Ward FE, Seignalet J, Payne R, Kissmeyer-Nielsen F, Gatti RA, Sachs JA, Lamm LU. The relation of parental sex and age to recombination in the HL-A system. Hum Hered. 1973; 23(3):197-205.
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Rowley PT, Jacobs M, Rosecrans C, Weitkamp LR, Doherty RA. High resolution analysis of hemoglobins: polyacrylamide isoelectric focusing. Biochem Med. 1972 Dec; 6(6):553-60.
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Spielman RS, Da Rocha FJ, Weitkamp LR, Ward RH, Neel JV, Chagnon NA. The genetic structure of a tribal population, the Yanomama indians. VII. Anthropometric differences among Yanomama villages. Am J Phys Anthropol. 1972 Nov; 37(3):345-56.
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Salzano FM, Neel JV, Weitkamp LR, Woodall JP. Serum proteins, hemoglobins and erythrocyte enzymes of Brazilian Cayapo Indians. Hum Biol. 1972 Sep; 44(3):443-58.
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Weitkamp LR, Neel JV. The genetic structure of a tribal population, the Yanomama Indians. IV. Eleven erythrocyte enzymes and summary of protein variants. Ann Hum Genet. 1972 Apr; 35(4):433-44.
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Weitkamp LR, Arends T, Gallango ML, Neel JV, Schultz J, Shreffler DC. The genetic structure of a tribal population, the Yanomama Indians. 3. Seven serum protein systems. Ann Hum Genet. 1972 Mar; 35(3):271-9.
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Winter WP, Weitkamp LR, Rucknagel DL. Amino acid substitution in two identical inherited human serum albumin variants: albumin Oliphant and albumin Ann Arbor. Biochemistry. 1972 Feb 29; 11(5):889-96.
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Lau TJ, Sunderman FW, Weitkamp LR, Agarwall SS, Sutnick AL, Blumberg BS, De Jimenez RB. Albumin cartago: a "new" slow-moving alloalbumin. Am J Clin Pathol. 1972 Feb; 57(2):247-51.
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Weitkamp LR, Adams MS, Rowley PT. Linkage between the MN- and Hb beta-loci? Hum Hered. 1972; 22(5):566-72.
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Weitkamp LR, Buck AA. Phenotype frequencies for four serum proteins in Afghanistan: two "new" albumin variants. Humangenetik. 1972; 15(4):335-40.
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Weitkamp LR. Genetic linkage relationships of the ADA and 6-PGD loci in "Humangenetik". Humangenetik. 1972; 15(4):359-60.
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Weitkamp LR, Guttormsen SA, Greendyke RM. Genetic linkage between a locus for 6-PGD and the Rh locus: evaluation of possible heterogeneity in the recombination fraction between sexes and among families. Am J Hum Genet. 1971 Sep; 23(5):462-70.
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Unusual albumin variants in Indonesians and Malayan aborigines. Hum Hered. 1971; 21(4):376-83.
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Weitkamp L, Neel JV. Gene frequencies and microdifferentiation among the Makiritare Indians. 3. Nine erythrocyte enzyme systems. Am J Hum Genet. 1970 Sep; 22(5):533-7.
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Arends T, Weitkamp LR, Gallango ML, Neel JV, Schultz J. Gene frequencies and microdifferentiation among the Makiritare Indians. II. Seven serum protein systems. Am J Hum Genet. 1970 Sep; 22(5):526-32.
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Stern AM, Gall JC, Perry BL, Stimson CW, Weitkamp LR, Poznanski AK. The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract. J Pediatr. 1970 Jul; 77(1):109-16.
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Chagnon NA, Neel JV, Weitkamp L, Gershowitz H, Ayres M. The influence of cultural factors on the demography and pattern of gene flow from the Makiritare to the Yanomama Indians. Am J Phys Anthropol. 1970 May; 32(3):339-49.
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Weitkamp LR, Guttormsen SA, Shreffler DC, Sing CF, Napier JA. Genetic linkage relations of the loci for 6-phosphogluconate dehydrogenase and adenosine deaminase in man. Am J Hum Genet. 1970 Mar; 22(2):216-20.
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Weitkamp LR, Renwick JH, Berger J, Shreffler DC, Drachmann O, Wuhrmann F, Braend M, Franglen G. Additional data and summary for albumin-Ge linkage in man. Hum Hered. 1970; 20(1):1-7.
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Weitkamp LR, Sing CF, Shreffler DC, Guttormsen SA. The genetic linkage relations of adenylate kinase: further data on the ABO-AK linkage group. Am J Hum Genet. 1969 Nov; 21(6):600-5.
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Weitkamp LR, Shreffler DC, Saave JJ. Serum albumin variants in New Guinea indigenes. Vox Sang. 1969 Sep; 17(3):237-40.
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Weitkamp LR, Janzen MK, Guttormsen SA, Gershowitz H. Inherited pericentric inversion of chromosome number two: a linkage study. Ann Hum Genet. 1969 Jul; 33(1):53-9.
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Weitkamp L. Chromosomal location of MN blood group locus. Science. 1969 Jun 6; 164(884):1187-8.
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Weitkamp LR, Basu A, Gall JC, Brown W. Albumin cayemite: a Negro plasma albumin variant. Humangenetik. 1969; 7(2):180-2.
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Weitkamp LR, Franglen G, Rokala DA, Polesky HF, Simpson NE, Sunderman FW, Bell HE, Saave J, Lisker R, Bohls SW. An electrophoretic comparison of human serum albumin variants: eight distinguishable types. Hum Hered. 1969; 19(2):159-69.
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Kueppers F, Holland PV, Weitkamp LR. Albumin Santa Ana: a new inherited variant. Hum Hered. 1969; 19(4):378-84.
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Weitkamp LR, Robson EB, Screffler DC, Corney G. An unusual human serum albumin variant: further data on genetic linkage between loci for human serum albumin and group-specific component (Ge). Am J Hum Genet. 1968 Jul; 20(4):392-7.
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Weitkamp LR, Chagnon NA. Albumin Máku: a new variant of human serum albumin. Nature. 1968 Feb 24; 217(5130):759-60.
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Arends T, Brewer G, Chagnon N, Gallango ML, Gershowitz H, Layrisse M, Neel J, Shreffler D, Tashian R, Weitkamp L. Intratribal genetic differentiation among the Yanomama Indians of southern Venezuela. Proc Natl Acad Sci U S A. 1967 May; 57(5):1252-9.
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Weitkamp LR, Shreffler DC, Robbins JL, Drachmann O, Adner PL, Wieme RJ, Simon NM, Cooke KB, Sandor G, Wuhrmann F, Braend M, Tárnoky AL. An electrophoretic comparison of serum albumin variants from nineteen unrelated families. Acta Genet Stat Med. 1967; 17(5):399-405.
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Weitkamp LR, Rucknagel DL, Gershowitz H. Genetic linkage between structural loci for albumin and group specific component (Gc). Am J Hum Genet. 1966 Nov; 18(6):559-71.
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DIXON HB, WEITKAMP LR. Conversion of the N-terminal serine residue of corticotrophin into glycine. Biochem J. 1962 Sep; 84:462-8.
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