Mark F. Leppert
#121,811
Most Influential Person Now
Mark F. Leppert's AcademicInfluence.com Rankings
Mark F. Leppertphilosophy Degrees
Philosophy
#5545
World Rank
#8376
Historical Rank
Logic
#2803
World Rank
#3849
Historical Rank
Mark F. Leppertbiology Degrees
Biology
#7426
World Rank
#10348
Historical Rank
Genetics
#709
World Rank
#801
Historical Rank
Molecular Biology
#858
World Rank
#881
Historical Rank
Download Badge
Philosophy Biology
Mark F. Leppert's Degrees
- PhD Molecular Biology Stanford University
- Doctorate Medicine Stanford University
Why Is Mark F. Leppert Influential?
(Suggest an Edit or Addition)Mark F. Leppert's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genetic alterations during colorectal-tumor development. (1988) (5548)
- A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
- Variable number of tandem repeat (VNTR) markers for human gene mapping. (1987) (1629)
- A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy (1997) (1331)
- A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns (1998) (1129)
- Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome (1993) (1107)
- A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes. (2007) (1107)
- A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family (1998) (906)
- Positional Cloning of the Human Quantitative Trait Locus Underlying Taste Sensitivity to Phenylthiocarbamide (2003) (813)
- Intra-individual change over time in DNA methylation with familial clustering. (2008) (689)
- The gene for familial polyposis coli maps to the long arm of chromosome 5. (1987) (674)
- Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 (1988) (648)
- The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome. (1992) (645)
- Mutation of the Stargardt Disease Gene (ABCR) in Age-Related Macular Degeneration (1997) (568)
- Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.213.3 (1990) (556)
- Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. (1991) (545)
- Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. (1993) (510)
- Future research directions in acute lung injury: summary of a National Heart, Lung, and Blood Institute working group. (2003) (504)
- The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis (1993) (427)
- A closely linked genetic marker for cystic fibrosis (1985) (423)
- Dihydropyridine receptor mutations cause hypokalemic periodic paralysis (1994) (413)
- Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD (2010) (400)
- Microsatellite instability in sporadic colon cancer is associated with an improved prognosis at the population level. (2001) (391)
- Methylenetetrahydrofolate reductase, diet, and risk of colon cancer. (1999) (382)
- Identification of a mutation in the gene causing hyperkalemic periodic paralysis (1991) (376)
- Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. (1997) (354)
- Associations between cigarette smoking, lifestyle factors, and microsatellite instability in colon tumors. (2000) (345)
- Benign familial neonatal convulsions linked to genetic markers on chromosome 20 (1989) (344)
- Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients (1990) (337)
- Relationship of Ki-ras mutations in colon cancers to tumor location, stage, and survival: a population-based study. (2000) (336)
- Allelic Loss in Colorectal Carcinoma (1989) (331)
- A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians. (1999) (314)
- Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia. (1998) (309)
- Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease. (1999) (307)
- Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome. (2008) (303)
- A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction (2008) (280)
- KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. (2003) (276)
- The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer. (2001) (264)
- Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps. (1990) (258)
- A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome (2009) (249)
- Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita (1992) (244)
- Clinical and pathological associations with allelic loss in colorectal carcinoma [corrected]. (1989) (234)
- Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1. (1996) (225)
- Precise localization of NF1 to 17q11.2 by balanced translocation. (1989) (222)
- Neuropathy target esterase gene mutations cause motor neuron disease. (2008) (213)
- Plus and minus strand leader rnas in negative strand virus-infected cells (1979) (213)
- Interaction of VSV leader RNA and nucleocapsid protein may control VSV genome replication (1981) (209)
- Seizure characteristics in chromosome 20 benign familial neonatal convulsions (1993) (208)
- Meat consumption, genetic susceptibility, and colon cancer risk: a United States multicenter case-control study. (1999) (207)
- Inverse relationship between microsatellite instability and K-ras and p53 gene alterations in colon cancer. (2001) (203)
- Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP). (2002) (202)
- Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5. (1988) (198)
- Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains. (1996) (192)
- Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis. (2004) (191)
- Gastric adenocarcinoma and dysplasia in fundic gland polyps of a patient with attenuated adenomatous polyposis coli. (1997) (186)
- A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7. (1993) (186)
- Heritability of X chromosome--inactivation phenotype in a large family. (1996) (176)
- NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network. (2000) (176)
- Alleles of APC modulate the frequency and classes of mutations that lead to colon polyps (1998) (163)
- Genetic linkage of Paget disease of the bone to chromosome 18q. (1997) (160)
- Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene. (2001) (158)
- Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novel ATP1A2 mutation (2004) (156)
- Genetic mapping of ossification of the posterior longitudinal ligament of the spine. (1998) (155)
- Sodium channel mutations in acetazolamide‐responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis (1994) (153)
- Cytogenetic and molecular analysis of sex-chromosome monosomy. (1988) (151)
- Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p (1995) (148)
- A mapped set of DNA markers for human chromosome 17. (1988) (148)
- Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus. (1991) (148)
- Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. (2002) (146)
- Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1. (1995) (146)
- A CA repeat 30-70 KB downstream from the adenomatous polyposis coli (APC) gene. (1991) (146)
- Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. (1993) (144)
- A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia. (2005) (144)
- Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p (2003) (142)
- Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q. (1990) (138)
- Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region. (1994) (137)
- Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization (2008) (136)
- Prognostic significance of p53 mutations in colon cancer at the population level (2002) (136)
- Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes. (2009) (134)
- Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q. (1995) (132)
- Genome Scans for Blood Pressure and Hypertension: The National Heart, Lung, and Blood Institute Family Heart Study* (2002) (127)
- BAT-26 and BAT-40 instability in colorectal adenomas and carcinomas and germline polymorphisms. (1999) (127)
- The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial (1999) (126)
- Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis (1993) (126)
- Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. (1991) (121)
- Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. (1987) (119)
- Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained (2013) (116)
- Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2. (1996) (114)
- Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. (1996) (113)
- Associations between dietary intake and Ki-ras mutations in colon tumors: a population-based study. (2000) (112)
- Further characterization of sendai virus DI-RNAs: A model for their generation (1977) (110)
- Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions. (2003) (109)
- The PHQ-9 as a brief assessment of lifetime major depression. (2007) (108)
- Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. (2003) (103)
- Genome-wide association study of Tourette Syndrome (2012) (102)
- A primary genetic linkage map for human chromosome 12. (1987) (101)
- Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q. (1999) (99)
- Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8+ T cells. (2010) (98)
- Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus: The NHLBI Family Heart Study (2000) (98)
- Genome-wide analyses identify common variants associated with macular telangiectasia type 2 (2017) (92)
- A detailed genetic map of the long arm of chromosome 11. (1990) (91)
- Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy (2001) (91)
- Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome (2016) (91)
- Possible association between autism and variants in the brain‐expressed tryptophan hydroxylase gene (TPH2) (2005) (90)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30]. (1988) (88)
- Associations between phenylthiocarbamide gene polymorphisms and cigarette smoking. (2005) (87)
- Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44). (1987) (86)
- Interindividual variability and parent of origin DNA methylation differences at specific human Alu elements. (2005) (86)
- Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1. (1994) (85)
- A primary genetic map of markers of human chromosome 10. (1988) (85)
- Cytogenetic and molecular studies of trisomy 13. (1987) (84)
- Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. (2009) (84)
- Etiological heterogeneity in X-linked spastic paraplegia. (1987) (83)
- Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. (2012) (81)
- Paroxysmal kinesigenic dyskinesia and infantile convulsions (2000) (80)
- Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript (2002) (80)
- A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study (2013) (80)
- NAT2, GSTM-1, cigarette smoking, and risk of colon cancer. (1998) (79)
- Polymorphisms in the Nonmuscle Myosin Heavy Chain 9 Gene (MYH9) Are Associated with Albuminuria in Hypertensive African Americans: The HyperGEN Study (2009) (78)
- Genome-Wide Linkage Analysis of Lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study (2001) (77)
- Fine Mapping and Identification of BMI Loci in African Americans. (2013) (75)
- A genome-wide affected sibpair linkage analysis of hypertension: the HyperGEN network. (2003) (75)
- Variants in the 5q31 cytokine gene cluster are associated with psoriasis (2008) (74)
- Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human (1998) (74)
- A high-density SNP genome-wide linkage scan in a large autism extended pedigree (2009) (74)
- Exome Analysis of a Family With Pleiotropic Congenital Heart Disease (2012) (72)
- Western diet, family history of colorectal cancer, NAT2, GSTM-1 and risk of colon cancer (2004) (71)
- A mapped set of genetic markers for human chromosome 9. (1988) (70)
- Community Engagement and Informed Consent in the International HapMap Project (2007) (70)
- (1)H nuclear magnetic resonance metabolomics analysis identifies novel urinary biomarkers for lung function. (2010) (70)
- Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. (1998) (69)
- Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms. (2010) (69)
- Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus. (1991) (68)
- A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. (1995) (67)
- Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis (2008) (67)
- A primary genetic map of chromosome 13q. (1986) (66)
- Locus heterogeneity of autosomal dominant long QT syndrome. (1993) (66)
- Hereditary Thrombophilia as a Model for Multigenic Disease (1999) (65)
- Mapping of the MYC gene to band 8q24.12----q24.13 by R-banding and distal to fra(8)(q24.11), FRA8E, by fluorescence in situ hybridization. (1991) (64)
- Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. (1992) (64)
- Allogeneic Hematopoietic Cell Transplantation for Metastatic Renal Cell Carcinoma after Nonmyeloablative Conditioning (2004) (64)
- Linkage of atypical myotonia congenita to a sodium channel locus (1992) (64)
- A longitudinal study of X-inactivation ratio in human females (2004) (64)
- Carriers of rare missense variants in IFIH1 are protected from psoriasis. (2010) (64)
- A primary map of ten DNA markers and two serological markers for human chromosome 19. (1988) (63)
- Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. (1988) (62)
- Ethnicity and human genetic linkage maps. (2005) (62)
- A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome (2017) (62)
- Characterization of a human 'midisatellite' sequence. (1987) (62)
- Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q. (1999) (61)
- SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex (2004) (59)
- Three secretory phospholipase A(2) genes that map to human chromosome 1P35-36 are not mutated in individuals with attenuated adenomatous polyposis coli. (1996) (58)
- An extended genetic linkage map of markers for human chromosome 10. (1988) (57)
- Discordance of T‐cell receptor β‐chain genes in familial multiple sclerosis (1991) (57)
- A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. (1995) (56)
- A CA-repeat polymorphism close to the adenomatous polyposis coli (APC) gene offers improved diagnostic testing for familial APC. (1993) (55)
- A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. (2003) (55)
- SSC polymorphisms in interleukin genes. (1994) (54)
- R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1) (1990) (53)
- Human Imprinted Chromosomal Regions Are Historical Hot-Spots of Recombination (2006) (52)
- Role of the beta 3-adrenergic receptor locus in obesity and noninsulin-dependent diabetes among members of Caucasian families with a diabetic sibling pair. (1996) (51)
- Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees. (1999) (51)
- American founder mutation for attenuated familial adenomatous polyposis. (2008) (50)
- Frequent recombination is observed in the distal end of the long arm of chromosome 14. (1989) (50)
- A mapped set of DNA markers for human chromosome 15. (1988) (49)
- High-sensitivity nanoLC-MS/MS analysis of urinary desmosine and isodesmosine. (2009) (48)
- Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2. (1997) (48)
- The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect (1999) (47)
- A molecular variant of the APC gene at codon 1822: its association with diet, lifestyle, and risk of colon cancer. (2001) (46)
- Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes. (1997) (45)
- Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation. (2008) (44)
- Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred. (1988) (43)
- Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations. (2002) (43)
- Rates of DNA synthesis in heterochromatic and euchromatic segments of the chromosome complements of two rodents. (1969) (41)
- A DNA probe for the LDL receptor gene is tightly linked to hypercholesterolemia in a pedigree with early coronary disease. (1986) (41)
- Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function. (2003) (41)
- Paroxysmal kinesigenic dyskinesia and infantile convulsions. Clinical and linkage studies. 2000. (2001) (39)
- Linkage Analysis of 19 Candidate Regions for Insulin Resistance in Familial NIDDM (1995) (39)
- A primary map of 24 loci on human chromosome 16. (1990) (39)
- Further evidence of a quantitative trait locus on chromosome 18 influencing postural change in systolic blood pressure: the Hypertension Genetic Epidemiology Network (HyperGEN) Study. (2005) (39)
- Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92,XXXY karyotype (2004) (38)
- Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms. (1985) (38)
- Personality and birth order in large families (2008) (38)
- Identification of a herpes simplex labialis susceptibility region on human chromosome 21. (2008) (37)
- Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population (2014) (36)
- Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated families. (1998) (35)
- Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings. (2002) (35)
- Human type II collagen gene (COL2A1) assigned to chromosome 12q13.1-q13.2 by in situ hybridization with biotinylated DNA probe (1989) (34)
- Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking (2013) (33)
- The Arg16Gly polymorphism of the β2-adrenergic receptor and left ventricular systolic function☆ (2003) (32)
- C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene. (2011) (32)
- The 5q31 variants associated with psoriasis and Crohn's disease are distinct (2008) (32)
- Autosomal dominant, familial spastic paraplegia, type I (1995) (31)
- Detailed genetic characterization of the interleukin-23 receptor in psoriasis (2008) (31)
- Genetic Linkage of the Dentinogenesis Imperfecta Type III Locus to Chromosome 4q (1999) (31)
- A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study (2002) (31)
- Feasibility of using genetic linkage analysis to identify the genes encoding T cell-defined minor histocompatibility antigens. (2002) (30)
- Further linkage data on cystic fibrosis: the Utah Study. (1986) (29)
- Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis. (1987) (28)
- Effect of defective interfering particles on plus- and minus- strand leader RNAs in vesicular stomatitis virus-infected cells (1980) (28)
- Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation. (1995) (27)
- Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigen. (1996) (27)
- Evidence for Linkage on Chromosome 3q25–27 in a Large Autism Extended Pedigree (2006) (27)
- A family‐based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia (2012) (27)
- Twelve loci form a continuous linkage map for human chromosome 18. (1988) (27)
- A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene. (1991) (26)
- Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36. (1994) (25)
- From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference project. (2008) (25)
- Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci (2017) (25)
- Coancestry in apparently sporadic primary pulmonary hypertension. (1995) (25)
- D2 dopamine receptor gene not linked to manic- depression in three families (1990) (25)
- Andreas Rett and benign familial neonatal convulsions revisited (2006) (25)
- ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies (2002) (24)
- Twenty-five loci form a continuous linkage map of markers for human chromosome 7. (1989) (23)
- Genetic mapping of adrenergic receptor genes in humans (1995) (23)
- Uncommon TGFBRI allele is not associated with increased susceptibility to colon cancer (2001) (23)
- Microcephaly with simplified gyral pattern in six related children. (1999) (23)
- Colonic Adenoma Risk in Familial Colorectal Cancer—A Study of Six Extended Kindreds (2008) (23)
- Setting Priorities for Genomic Research (2004) (22)
- THE GENE FOR FAMILIAL POLYPOSIS MAPS TO THE LONG ARM OF CHROMOSOME-5 (1987) (22)
- TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study. (2004) (22)
- Linkage analysis of Tourette syndrome in a large utah pedigree (2010) (22)
- Isolation and mapping of a polymorphic DNA sequence (pEKMDA2-I) on chromosome 16 [D16S83]. (1988) (21)
- Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation. (2004) (21)
- A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis (2018) (21)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]. (1988) (20)
- Analysis of a Scottish founder effect narrows the TAPVR‐1 gene interval to chromosome 4q12 (2006) (20)
- Identification of Distinct Plasma Biomarker Signatures in Patients with Rapid and Slow Declining Forms of COPD (2011) (20)
- The inducible prostaglandin biosynthetic enzyme, cyclooxygenase 2, is not mutated in patients with attenuated adenomatous polyposis coli. (1998) (20)
- Rapid molecular analysis of the STAT3 gene in Job syndrome of hyper-IgE and recurrent infectious diseases. (2010) (20)
- A Rare Variant in CACNA1D Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree (2016) (20)
- Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22. (1992) (19)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ32) on chromosome 4p [D4S125]. (1988) (19)
- Isolation and mapping of a polymorphic DNA sequence pMLJ14 on chromosome 14 [D14S13] (1988) (19)
- Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15). (1987) (19)
- Susceptibility genes in human epilepsy. (1999) (19)
- Isolation and mapping of a polymorphic DNA sequence (pCMM86) on chromosome 17q [D17S74]. (1988) (19)
- Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84]. (1988) (18)
- Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 [D10S15] (1988) (17)
- Isolation and mapping of a polymorphic DNA sequence (pEFD145) on chromosome 3 [D3S32]. (1988) (17)
- Exome analysis of a family with Wolff–Parkinson–White syndrome identifies a novel disease locus (2015) (17)
- Genetic linkage analysis in familial benign hypercalcemia using a candidate gene strategy. I. Studies in four families. (1992) (16)
- Chromosome instability and the FAMMM syndrome. (1993) (16)
- No linkage of the lipoprotein lipase locus to hypertension in Caucasians. (1999) (16)
- Benign familial neonatal epilepsy with mutations in two potassium channel genes. (1999) (16)
- The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89. (1993) (16)
- A genetic linkage map of markers for human chromosome 20. (1989) (16)
- AGT genetic variation, plasma AGT, and blood pressure: An analysis of the Utah Genetic Reference Project pedigrees. (2010) (16)
- Multivariate characterization of white matter heterogeneity in autism spectrum disorder (2017) (15)
- Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations (2016) (15)
- Germline mutation rates in young adults predict longevity and reproductive lifespan (2019) (15)
- Isolation and mapping of a polymorphic DNA sequence pEFD126.3 on chromosome 9q (D9S7). (1987) (15)
- The Arg16Gly polymorphism of the beta2-adrenergic receptor and left ventricular systolic function. (2003) (14)
- Construction of human genetic linkage maps: I. Progress and perspectives. (1986) (14)
- Corrigendum SSC polymorphisms in interleukin genes (1995) (14)
- Searching for Human Epilepsy Genes: A Progress Report (1993) (14)
- Colorectal adenomas and cancer link to chromosome 13q22.1–13q31.3 in a large family with excess colorectal cancer (2010) (14)
- Isolation and mapping of a polymorphic DNA sequence (pRMR6) on chromosome 20 [D20S20]. (1988) (14)
- A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22 (2009) (13)
- Isolation and mapping of a polymorphic DNA sequence (pCMM6) on chromosome 20 [D20S19]. (1988) (13)
- Localization to chromosome 11 of a gene encoding a human minor histocompatibility antigen. (1998) (12)
- Isolation and mapping of a polymorphic DNA sequence pYNH15 on chromosome 12q [D12S17]. (1988) (12)
- Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study (2004) (12)
- Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4]. (1988) (12)
- Isolation and mapping of a polymorphic DNA sequence pYNZ86.1 on chromosome 3 (D3S30). (1987) (12)
- Isolation and mapping of a polymorphic DNA sequence pEFD33.2 on chromosome 12 [D12S14]. (1988) (11)
- Do non-insulin-dependent diabetes mellitus (NIDDM) and insulin-dependent diabetes mellitus (IDDM) share genetic susceptibility loci? An analysis of putative IDDM susceptibility regions in familial NIDDM. (1997) (11)
- Identification of cystic fibrosis mutations. (1991) (11)
- Isolation and mapping of a polymorphic DNA sequence (pMCT108.2) on chromosome 18 [D18S24]. (1988) (11)
- Isoelectric focusing of superoxide dismutase: report of the unique SOD A*2 allele in a US white population. (1988) (11)
- Isolation and mapping of a polymorphic DNA sequence pHBI59 on chromosome 11 [D11S146] (1988) (10)
- Evidence of genetic heterogeneity among the nondystrophic myotonias (1992) (10)
- Report of the committee on the genetic constitution of chromosome 2. (1990) (10)
- Discordance of T-cell receptor beta-chain genes in familial multiple sclerosis. (1991) (10)
- Isolation and mapping of a polymorphic DNA sequence pHHH202 on chromosome 17 [D17S33]. (1988) (10)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ31) on chromosome 22 [D22S32]. (1988) (9)
- Linkage of DNA probe B79a (D7S13) to cystic fibrosis. (1987) (9)
- Isolation and mapping of a polymorphic DNA sequence MCT128.1 on chromosome 11 [D11S285] (1988) (9)
- Isolation and mapping of a polymorphic DNA sequence (pMCA1-1) on chromosome 15 [D15S33]. (1988) (9)
- Isolation and mapping of a polymorphic DNA sequence (pHHH157) on chromosome 6p [D6S29]. (1988) (9)
- Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (D1S58) (1987) (9)
- A closely linked genetic marker for cystic fibrosis (1986) (9)
- Isolation and mapping of a polymorphic DNA sequence (pHBI59) on chromosome 11 [D11S146]. (1988) (9)
- Isolation and mapping of a polymorphic DNA sequence pYNH37.3 on chromosome 17p [D17S28]. (1988) (9)
- The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees (2005) (9)
- Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia. (2018) (8)
- Erratum: Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions (Human Molecular Genetics (2003) vol. 12 (1569-1578)) (2004) (8)
- Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium. (1992) (8)
- Isolation and mapping of a polymorphic DNA sequence pEKH7.4 to chromosome 1 (D1S65). (1987) (8)
- Gene Mapping and Other Tools for Discovery (1990) (8)
- The identical 5′ splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect (2000) (8)
- Isolation and mapping of a polymorphic DNA sequence for NRAS pMCR3 on chromosome 1. (1987) (8)
- Isolation and mapping of a polymorphic DNA sequence (pMCT15) on chromosome 21 [D21S113]. (1988) (8)
- Isolation and mapping of a polymorphic DNA sequence pMCT35.1 on chromosome 17p [D17S31]. (1988) (7)
- Isolation and mapping of a polymorphic DNA sequence (pYNH3) on chromosome X [DXS287]. (1988) (7)
- Erratum: A CA repeat 30-70 Kb downstream from the adenomatous polyposis coli (APC) gene (Nucleic Acids Research (1991) 19 (6348)) (1992) (7)
- Analysis of microtubule-associated protein 1a gene in hereditary spastic paraplegia (1998) (7)
- Isolation and mapping of a polymorphic DNA sequence (pTB10.163) on chromosome 10 [D10S22]. (1988) (7)
- A Gene for Primary Congenital Glaucoma Is Not Linked to the Locus on Chromosome lq for Autosomal Dominant Juvenile‐Onset Open Angle Glaucoma (1996) (7)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ13) on chromosome 1p [D1S64]. (1988) (6)
- Isolation and mapping of a polymorphic DNA sequence pRMU3 on chromosome 17q [D17S24]. (1988) (6)
- Identification and mapping of RFLPs for human tissue factor (HTF) to chromosome 1p. (1987) (6)
- Isolation and mapping of a polymorphic DNA sequence cEFD52 on chromosome 17q [D17S26]. (1988) (6)
- A CA repeat 30-70 Kb downstream from the adenomatous polyposis coli (APC) gene. (1992) (6)
- Isolation and mapping of a polymorphic DNA sequence (pEFD49.3) on chromosome 15 [Dl5S29] (1988) (6)
- Isolation and mapping of a polymorphic DNA sequence pJCZ3.1 on chromosome 19 [D19S20]. (1988) (6)
- Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study. (1999) (6)
- Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations (2010) (6)
- 5' Terminus of defective and nondefective Sendai viral genomes is ppp Ap (1978) (6)
- Isolation and mapping of a polymorphic DNA sequence pEKZ19.3 on chromosome 9q (D9S17). (1987) (5)
- Isolation and mapping of a polymorphic DNA sequence (pEFD64.2) on chromosome 3 [D3S46]. (1988) (5)
- Isolation and mapping of a polymorphic DNA sequence (pMCOA12) on chromosome 9q [D9S28]. (1988) (5)
- The discovery of epilepsy genes by genetic linkage. (1991) (5)
- A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis. (2018) (5)
- Isolation and mapping of a polymorphic DNA sequence (pTHH26) on chromosome 11 [D11S149]. (1988) (5)
- Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene. (1994) (4)
- Isolation and mapping of a polymorphic DNA sequence pMHZ15 on chromosome 10 [D10S17] (1988) (4)
- Isolation and mapping of a polymorphic DNA sequence pMHZ14 on chromosome 1p (D1S60). (1987) (4)
- Isolation and mapping of a polymorphic DNA sequence (pCMM1.2) on chromosome 12q [D12S15]. (1988) (4)
- MammalianX-chromosomes: A new kind of composite-typeX in the voleArvicola scherman exitus miller (1968) (4)
- Isolation and mapping of a polymorphic DNA sequence (pJCZ30) on chromosome 6 [D6S37]. (1988) (4)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15 [Dl5S45] (1988) (4)
- Isolation and mapping of a polymorphic DNA sequence (pTHH55) on chromosome. (1988) (4)
- Isolation and mapping of a polymorphic DNA sequence pHBI18P2 on chromosome 11 [D11S147] (1988) (3)
- Isolation and mapping of a polymorphic DNA sequence (cMHZ47) on chromosome 13 [D13S52]. (1988) (3)
- Isolation and mapping of a polymorphic DNA sequence pYNM3 on chromosome 8 (D8S38). (1987) (3)
- Isolation and mapping of a polymorphic DNA sequence (pHHH163) on chromosome 18 [D18S21]. (1988) (3)
- Isolation and mapping of a polymorphic DNA sequence (pMCT128.2) on chromosome 8 [D8S39]. (1988) (3)
- Isolation and mapping of a polymorphic DNA sequence pMHZ10 on chromosome 9q (D9S11). (1987) (3)
- Isolation and mapping of a polymorphic DNA sequence (pJCZ67) on chromosome 7 [D7S396]. (1988) (3)
- Isolation and mapping of a polymorphic DNA sequence pEFD4.2 on chromosome 19 [D19S22]. (1988) (3)
- Isolation and mapping of a polymorphic DNA sequence (pKKA12) on chromosome 7 [D7S398]. (1988) (3)
- Corrigendum: SSC Polymorphisms in interleukin genes(Human Molecular Genetics(1994)3(1710)) (1995) (3)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40]. (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence (pRMU7.4) on chromosome 7p [D7S370]. (1988) (2)
- Mouse Models of Benign Familial Neonatal Convulsions (BFNC): Mutations in KCNQ (Kv7) Genes (2009) (2)
- Isolation and mapping of a polymorphic DNA sequence (pHHH171) on chromosome 6p [D6S38]. (1988) (2)
- Evaluation of heterodimeric guanylyl cyclase genes as candidates for human hypertension (2000) (2)
- Corrigendum: A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis [Human Molecular Genetics, 27, 13, (2018), (2383-2391)] DOI: 10.1093/hmg/ddy132 (2018) (2)
- Isolation and mapping of a polymorphic DNA sequence pEKZ105 on chromosome 2 (D2S55). (1987) (2)
- Nonsyndromic seizure disorders: epilepsy and the use of the internet to advance research. (2003) (2)
- Isolation and mapping of a polymorphic DNA sequence (pYNM18.1) on chromosome 15 [D15S35]. (1988) (2)
- No evidence of linkage between the very-low-density lipoprotein receptor gene and fasting serum insulin or homeostasis model assessment insulin resistance index: the National Heart, Lung, and Blood Institute Family Heart Study. (2000) (2)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40]. (1988) (2)
- Factor V Leiden is not common in patients diagnosed with primary pulmonary hypertension. (1998) (2)
- Genes for rare idiopathic generalized epilepsies: BFNC. (1999) (2)
- Isolation and mapping of a polymorphic DNA sequence (pHHH106) on chromosome 1 [D1S67]. (1988) (2)
- Isolation of mapping of a polymorphic DNA sequence pEFZ10 on chromosome 18 [D18S22]. (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence pHHH122 on chromosome 2 (D2S54) (1987) (2)
- Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p [D1S62]. (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence (pHHH119) on chromosome 1 [D1S59]. (1988) (2)
- A Single Nucleotide Polymorphism in CD19 Defines a Novel Target for Immunotherapy of B Cell Malignancies with CD4+ Cytotoxic T Cells. (2007) (2)
- Mapping approaches to gene identification in humans. (1987) (2)
- Isolation and mapping of a polymorphic DNA sequence (pTHIZ53) on chromosome 12 [D12S18]. (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence (pEFD53.2) on chromosome 1 [D1S73]. (1988) (2)
- A genetic linkage map with 29 loci spanning human chromosome 13q. (1993) (2)
- Isolation and mapping of a polymorphic DNA sequence (pEFD64.1) on chromosome 3. (1988) (1)
- Contents Vol. 55, 1990 (1990) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD6) chromosome 6 [D6S41]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMCOC14) on chromosome 4p [D4S124] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (cYNA4) on chromosome 2 [D2S50]. (1988) (1)
- Determination and Assessment of Extended Haplotypes Spanning the Chromosome 1q32 CFH-To-CFHR5 Locus (2010) (1)
- Eldon Gardner Memorial Lecture: Genetic Mapping and Allelic Heterogeneity of the Familial Polyposis Gene (1990) (1)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ15) on chromosome 2 [D2S50]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD85.7) on chromosome 15 [D15S37] (1988) (1)
- Hereditary spastic paraplegia linked to chromosome 15q (1996) (1)
- Polymorphic Peptide Hair Project (2014) (1)
- Erratum: The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect (Human Genetics (1999) 105 (388-398)) (2000) (1)
- Human Genetic Mapping and Inherited Deafness Syndromes (1991) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMCOC12) on chromosome 14 [D14S20] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ94) on chromosome 17 [D17S80]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMHZ21) on chromosome 9q [D9S30]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD49.2) on chromosome 15. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pYNZ9.1 on chromosome 2 (D2S46). (1987) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD70.3) on chromosome 18 [D18S23]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pMCT136 on chromosome 9q (D9S10). (1987) (1)
- Isolation and mapping of a polymorphic DNA sequence (pYNA15.2) on chromosome 15 [D13S36] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pHBI40 on chromosome 1 (D1S66). (1987) (1)
- Setting priorities for genomic research [2] (multiple letters) (2004) (1)
- An anonymous single-copy clone, p30-1-60, identifies a frequent RFLP on chromosome 3p [HGM9 no. D3S86]. (1989) (1)
- Isolation and mapping of a polymorphic DNA sequence (pTB10.171) on chromosome 10 [D10S19]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pTBAB5.7 on chromosome 2 (D2S47). (1987) (1)
- Isolation and mapping of a polymorphic DNA sequence pMCT46.2 on chromosome 15 [D15S26]. (1988) (1)
- The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. (2009) (1)
- Isolation and mapping of a polymorphic DNA sequence pEKZ104.1 on chromosome 15 [D15S30]. (1988) (1)
- D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7 (1991) (1)
- Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9). (1987) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMCT149.2) on chromosome 15 [D15S34] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pKKA35) on chromosome 17 [D17S75]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (cKKA39) on chromosome 14 [D14S23]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pHHH208) on chromosome 14 [D14S19]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pCMM66) on chromosome 14 [D14S22] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pYNZ90.1 on chromosome 15 [D15S28]. (1988) (1)
- Upper gastrointestinal phenotype and risk of cancer in attenuated adenomatous polyposis coli (2003) (0)
- Familial patterns in speech and fluency: Studies in variable expression (2000) (0)
- HETEROGENEITY IN X-LINKED SPASTIC PARAPLEGIA (1987) (0)
- Phenylthiocarbamide Locus Underlying Taste Sensitivity to Positional Cloning of the Human Quantitative Trait (2007) (0)
- Chromosomal disorders of the unborn. (1968) (0)
- Isolation and mapping of a polymorphic DNA sequence pYNM17 on chromosome 9q (D9S6). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence pEFZ18.2 on chromosome 14 [D14S17] (1988) (0)
- FineStructure DNA Mapping Studies oftheChromosomal Region Harboring theGenetic Defect in Neurofibromatosis TypeI (1989) (0)
- Subject Index Vol. 60, 2005 (2006) (0)
- Broad scan linkage analysis in a large Tourette family pedigree (1994) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMCT32.1) on chromosome 3 [D3S31]. (1988) (0)
- The genetics of gastrointestinal polyposis: Identification of the adenomatous polyposis coli gene (1993) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMCT149.2) on chromosome 15. (1988) (0)
- The most recent and extensive genome-wide human genetic linkage maps (2005) (0)
- Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer (2010) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMI37) on chromosome 7 [D7S368]. (1988) (0)
- ABCA4 Mutational Analysis in a Cohort of 30 Recessive Retinitis Pigmentosa Families (2004) (0)
- Isolation and mapping of a polymorphic DNA sequence (pKKA40) on chromosome 9q [D9S31]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFD52.1) on chromosome 15. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH22) on chromosome 9 [D9S12]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMHZ13) on chromosome 9q [D9S13]. (1988) (0)
- Characterization of a human 'midisaleUite' sequence (2005) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMCT106) on chromosome 2 [D2S61]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pEFD122 on chromosome 2 (D2S48). (1987) (0)
- D7S449 detects a HindIII polymorphism tightly linked to the MET gene on chromosome 7. (1990) (0)
- Isolation and mapping of a polymorphic DNA sequence (cMCOD13) on chromosome 3 [D3S44]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pYNA15.2) on chromosome 15 [D15S36]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMHZ17) on chromosome 13 [D13S51]. (1988) (0)
- Contents Vol. 29, 2009 (2009) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH152 on chromosome 17q [D17S32]. (1988) (0)
- Gastrointestinal polyposis and nonpolyposis syndromes. (1995) (0)
- SSC polymorphisms in interleukin genes. (1994) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMCT96.1 and pMCT96.2) on chromosome 9q [D9S14]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFD49.3) on chromosome 15. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH115.2 on chromosome 2 (D2S54). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (DIS58). (1987) (0)
- enetic Testing and Phenotype in a Large Kindred With ttenuated Familial Adenomatous Polyposis (2004) (0)
- Isolation and mapping of a polymorphic DNA sequence pYNZ156 on chromosome 10 [D10S18] (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH14) on chromosome 12p [D12S16]. (1988) (0)
- DNA markers for the cystic fibrosis locus. (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371]. (1988) (0)
- Instability in 18S and 5.8S rDNA copy numbers and 18S:5.8S ratios in longitudinally-collected human DNA samples detected by monochrome multiplex qPCR (2018) (0)
- The Role of NAC in Amyloidogenesis in Alzheimer’s Disease (2000) (0)
- Isolation and mapping of a polymorphic DNA sequence pEFD40.3 on chromosome 9 (D9S8). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM17.4) on chromosome 10 [D10S23]. (1988) (0)
- Session III: Future types of screening: A prospectus A: DNA analysis (1990) (0)
- A hypervariable region at the D19S11 locus (1987) (0)
- [Karyotype, heterochromatin and DNA-content in 13 species of voles (Microtinae, Mammalia-Rodentia)]. (1968) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15. (1988) (0)
- Signal-averaged electrocardiography improves patient characterization in hypertrophic cardiomyopathy and aids localization of a disease gene to chromosome 2p in a linkage analysis study (1991) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH133 on chromosome 2 (D2S45). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ38) on chromosome 2 [D2S60]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pRMU1 on chromosome 17q [D17S27]. (1988) (0)
- A chromosome 16 locus for familial leukemia. (1997) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM63) on chromosome 2 [D2S51]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pYNH20) on chromosome 13 [D13S50]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (MCT117) on chromosome 11 [D11S145]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371]. (1988) (0)
- Un-kyung Kim Taste Sensitivity to Phenylthiocarbamide Positional Cloning of the Human Quantitative Trait Locus Underlying (2013) (0)
- Isolation and mapping of a polymorphic DNA sequence (cMCOE32) on chromosome 2 [D2S53] (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH220 on chromosome 9p (D9S27). (1987) (0)
- Characterization of the Psoriasis-associated IL12B and IL23R Genes (2007) (0)
- Isolation and mapping of a polymorphic DNA sequences (pTHH28) on chromosome 7p (1988) (0)
- Genetic Analysis of Ion Transport (1992) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMI40) on chromosome 13 [D13S49]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pMHZ9 on chromosome 14 [D14S18] (1988) (0)
- Contents Vol. 60, 2005 (2006) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM62) on chromosome 14 [D14S21]. (1988) (0)
- Subject Index Vol. 29, 2009 (2009) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM17.1) on chromosome 10 [D10S16]. (1988) (0)
- Germline mutation rates in young adults predict longevity and reproductive lifespan (2020) (0)
- Isolation and mapping of a polymorphic DNA sequence (cMCOC46) on chromosome 13 [D13S54]. (1988) (0)
- Lipid loci with multiple signals in Europeans. (2013) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH37) on chromosome 14 [D14S16]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMC96.1 and pMCT96.2) on chromosome 9q (1988) (0)
- Abstract MP60: Fine Mapping of Body Fat Distribution Loci in African American Populations: The Population Architecture Using Genomics and Epidemiology (PAGE) Study (2014) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFD134.7) on chromosome 3 [D3S45]. (1988) (0)
- Linkage Maps of Human Genes (1987) (0)
- Brief Communication ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies ILAE Genetics Commission (2002) (0)
This paper list is powered by the following services:
What Schools Are Affiliated With Mark F. Leppert?
Mark F. Leppert is affiliated with the following schools:
