Dr. David E. Comings

Dr. David E. Comings's AcademicInfluence.com Rankings

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Dr. David E. Comings

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Dr. David E. Comings'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

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes (2004) (1461)
The Reward Deficiency Syndrome: A Biogenetic Model for the Diagnosis and Treatment of Impulsive, Addictive and Compulsive Behaviors (2000) (898)
Reward deficiency syndrome: genetic aspects of behavioral disorders. (2000) (646)
The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders. (1991) (583)
REWARD DEFICIENCY SYNDROME (1996) (513)
A general theory of carcinogenesis. (1973) (464)
The D2 Dopamine Receptor Gene as a Determinant of Reward Deficiency Syndrome (1996) (439)
Familial multifocal fibrosclerosis. Findings suggesting that retroperitoneal fibrosis, mediastinal fibrosis, sclerosing cholangitis, Riedel's thyroiditis, and pseudotumor of the orbit may be different manifestations of a single disease. (1967) (396)
Metabolic basis of inherited disease (1983) (361)
A study of the dopamine D2 receptor gene in pathological gambling. (1996) (354)
Molecular heterosis: a review. (2000) (337)
The mechanism of C- and G-banding of chromosomes. (1973) (290)
Mechanisms of chromosome banding and implications for chromosome structure. (1978) (285)
Studies of the 48 bp repeat polymorphism of the DRD4 gene in impulsive, compulsive, addictive behaviors: Tourette syndrome, ADHD, pathological gambling, and substance abuse. (1999) (284)
Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: the additive and subtractive effect of the three dopaminergic genes--DRD2, D beta H, and DAT1. (1996) (275)
Dopamine D2 receptor gene variants: association and linkage studies in impulsive-addictive-compulsive behaviour. (1995) (271)
The dopamine D2 receptor (DRD2) gene: a genetic risk factor in smoking. (1996) (270)
Association of the dopamine transporter gene (DAT1) with poor methylphenidate response. (1999) (258)
Studies of the potential role of the dopamine D1 receptor gene in addictive behaviors (1997) (243)
A controlled study of Tourette syndrome. I. Attention-deficit disorder, learning disorders, and school problems. (1987) (236)
The structure and function of chromatin. (1972) (227)
Dopamine D2 receptor (DRD2) gene and susceptibility to posttraumatic stress disorder: A study and replication (1996) (225)
Principles and techniques of electron microscopy: Biological applications (1971) (214)
Activation instead of blocking mesolimbic dopaminergic reward circuitry is a preferred modality in the long term treatment of reward deficiency syndrome (RDS): a commentary (2008) (191)
The rationale for an ordered arrangement of chromatin in the interphase nucleus. (1968) (190)
Nuclear proteins. III. The fibrillar nature of the nuclear matrix. (1976) (186)
An epidemiologic study of Tourette's syndrome in a single school district. (1990) (183)
Cannabinoid receptor gene (CNR1): association with IV drug use (1997) (179)
Tourette syndrome: clinical and psychological aspects of 250 cases. (1985) (177)
Tourette's syndrome and attention deficit disorder with hyperactivity: are they genetically related? (1984) (177)
Attention-deficit-hyperactivity disorder and reward deficiency syndrome (2008) (170)
Initiation of deoxyribonucleic acid replication at the nuclear membrane in human cells. (1968) (169)
Comparison of the role of dopamine, serotonin, and noradrenaline genes in ADHD, ODD and conduct disorder: multivariate regression analysis of 20 genes (2000) (164)
Are dopaminergic genes involved in a predisposition to pathological aggression? Hypothesizing the importance of "super normal controls" in psychiatricgenetic research of complex behavioral disorders. (2005) (158)
The dopamine D2 receptor gene: a genetic risk factor in substance abuse. (1994) (158)
Multivariate analysis of associations of 42 genes in ADHD, ODD and conduct disorder (2000) (155)
The eighth day of creation. (1980) (152)
Arrangement of chromatin in the nucleus (1980) (147)
Parent-daughter transmission of the androgen receptor gene as an explanation of the effect of father absence on age of menarche. (2002) (147)
Clinical and Molecular Genetics of ADHD and Tourette Syndrome (2001) (141)
Association of chromatin fibers with the annuli of the nuclear membrane. (1970) (139)
Human dopamine transporter gene: coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations (2000) (138)
The dopamine D2 receptor (DRD2) as a major gene in obesity and height. (1993) (136)
Genetic variants of the human obesity (OB) gene: association with body mass index in young women, psychiatric symptoms, and interaction with the dopamine D2 receptor (DRD2) gene. (1996) (135)
Molecular Mechanisms of Chromosome Pairing, Folding and Function (1971) (135)
Polygenic inheritance and micro/minisatellites (1998) (134)
Tourette Syndrome and Human Behavior (1990) (131)
Association of polymorphisms of dopamine D2 receptor (DRD2), and dopamine transporter (DAT1) genes with schizoid/avoidant behaviors (SAB) (1997) (130)
Detection of major gene for Gilles de la Tourette syndrome. (1984) (124)
Sexually dimorphic effect of the Val66Met polymorphism of BDNF on susceptibility to Alzheimer's disease: New data and meta‐analysis (2009) (118)
Generational Association Studies of Dopaminergic Genes in Reward Deficiency Syndrome (RDS) Subjects: Selecting Appropriate Phenotypes for Reward Dependence Behaviors (2011) (118)
Additive effect of three noradrenergic genes (ADRA2A, ADRA2C, DBH) on attention‐deficit hyperactivity disorder and learning disabilities in Tourette syndrome subjects (1999) (113)
Evidence for Ancient Tetraploidy and Conservation of Linkage Groups in Mammalian Chromosomes (1972) (110)
The Molecular Genetics of Pathological Gambling (1998) (108)
DOPAMINE RECEPTOR GENES ARE ASSOCIATED WITH AGE AT FIRST SEXUAL INTERCOURSE (1999) (105)
Pc 1 Duarte, a common polymorphism of a human brain protein, and its relationship to depressive disease and multiple sclerosis (1979) (101)
Clinical and genetic relationships between autism-pervasive developmental disorder and Tourette syndrome: a study of 19 cases. (1991) (100)
Stress as a mediating factor in the association between the DRD2 TaqI polymorphism and alcoholism. (2001) (99)
A controlled study of Tourette syndrome. VII. Summary: a common genetic disorder causing disinhibition of the limbic system. (1987) (98)
Fine structure of kinetochore in Indian muntjac. (1971) (97)
A controlled study of Tourette syndrome. V. Depression and mania. (1987) (96)
Heterochromatin of the Indian muntjac. Replication, condensation, DNA ultracentrifugation, fluorescent and heterochromatin staining. (1971) (92)
Blood serotonin and tryptophan in Tourette syndrome. (1990) (85)
Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3. (1996) (84)
Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders. (2001) (82)
Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse (1998) (81)
The chromatoid body in mouse spermatogenesis: evidence that it may be formed by the extrusion of nucleolar components. (1972) (80)
Optical studies of the interaction of 4′-6-diamidino-2-phenylindole with DNA and metaphase chromosomes (1977) (79)
Electron microscopy of human fibroblasts in tissue culture during logarithmic and confluent stages of growth. (1970) (78)
A controlled study of Tourette syndrome. IV. Obsessions, compulsions, and schizoid behaviors. (1987) (78)
DNA of mammalian and avian heterochromatin. (1972) (77)
DNA replication and the nuclear membrane. (1973) (77)
Nuclear proteins. II. Similarity of nonhistone proteins in nuclear sap and chromatin, and essential absence of contractile proteins from mouse liver nuclei (1976) (77)
Association of nuclear membrane fragments with metaphase and anaphase chromosomes as observed by whole mount electron microscopy. (1970) (76)
Why different rules are required for polygenic inheritance: lessons from studies of the DRD2 gene. (1998) (75)
Association between the cannabinoid receptor gene (CNR1) and the P300 event-related potential (1997) (75)
Mechanisms of chromosome banding. II. Evidence that histones are not involved. (1974) (73)
A controlled study of Tourette syndrome. II. Conduct. (1987) (73)
Association of the androgen receptor gene (AR) with ADHD and conduct disorder. (1999) (73)
Dopamine D2 receptor gene (DRD2) haplotypes and the defense style questionnaire in substance abuse, Tourette syndrome, and controls (1995) (72)
Holocentric chromosomes in Oncopeltus: kinetochore plates are present in mitosis but absent in meiosis (2004) (71)
A search for protein cores in chromosomes: is the scaffold an artifact? (1980) (70)
Association of the muscarinic cholinergic 2 receptor (CHRM2) gene with major depression in women. (2002) (70)
A controlled study of Tourette syndrome. VI. Early development, sleep problems, allergies, and handedness. (1987) (68)
The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation. (1986) (67)
Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene (1993) (67)
HISTONES OF GENETICALLY ACTIVE AND INACTIVE CHROMATIN (1967) (67)
Oxford companion to animal behavior (1988) (66)
A controlled family history study of Tourette's syndrome, I: Attention-deficit hyperactivity disorder and learning disorders. (1990) (66)
A storage form of ribosomes in mouse oocytes. (1971) (63)
Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease). (1975) (62)
Mechanisms of chromosome banding (1975) (62)
Mechanisms of chromosome banding (1975) (60)
Mechanism of Chromosome Pairing during Meiosis (1970) (60)
Whole-mount electron microscopy of the centromere region of metacentric and telocentric mammalian chromosomes. (1970) (59)
Association of the serotonin transporter gene with serum cholesterol levels and heart disease. (1999) (58)
Serotonin transporter gene polymorphisms in alcohol dependence. (2000) (57)
The duration of replication of the inactive X chromosome in humans based on the persistence of the heterochromatic sex chromatin body during DNA synthesis. (1967) (56)
A controlled study of Tourette syndrome. III. Phobias and panic attacks. (1987) (55)
Similarities in the cytoplasmic proteins of different organs and species examined by SDS gel electrophoresis. (1972) (54)
THE INACTIVE X CHROMOSOME (1966) (54)
Exon and intron variants in the human tryptophan 2,3-dioxygenase gene: potential association with Tourette syndrome, substance abuse and other disorders. (1996) (54)
Condensation of chromosomes onto the nuclear membrane during prophase. (1970) (53)
Mechanisms of chromosome banding (2004) (52)
Nuclear proteins. I. Electrophoretic comparison of mouse nucleoli, heterochromatin, euchromatin and contractile proteins. (1975) (51)
Incorporation of tritium of 3H-5-uridine into DNA. (1966) (51)
Non-histone proteins. The effect of nuclear washes and comparison of metaphase and interphase chromatin. (1973) (51)
Risk of late-onset Alzheimer's Disease associated with BDNF C270T polymorphism (2005) (50)
Buoyant density and satellite composition of DNA of mouse heterochromatin. (1971) (49)
Mechanisms of chromosome banding (2004) (49)
Molecular heterosis as the explanation for the controversy about the effect of the DRD2 gene on dopamine D2 receptor density (1999) (49)
Tourette syndrome: a hereditary neuropsychiatric spectrum disorder. (1994) (48)
Higher order structure of chromosomes (1979) (48)
Myeloblastoma preceding blood and marrow evidence of acute leukemia (1965) (48)
RANTES: a genetic risk marker for multiple sclerosis (2004) (48)
Variants of the orexin2/hcrt2 receptor gene identified in patients with excessive daytime sleepiness and patients with Tourette's syndrome comorbidity (2004) (48)
Genetic factors in substance abuse based on studies of Tourette syndrome and ADHD probands and relatives. I. Drug abuse. (1994) (47)
Minds made feeble: The myth and legacy of the Kallikaks. (1985) (47)
The chromosomes and DNA of Allium cepa (2004) (46)
A serotonin receptor gene (5HT1A) variant found in a Tourette's syndrome patient. (1996) (46)
Whole mount electron microscopy of meiotic chromosomes and the synaptonemal complex (2004) (46)
Hypothesis: homozygosity in Tourette syndrome. (1989) (46)
Partial deletion of chromosome 6p: delineation of the syndrome. (1991) (46)
Studies of the c-Harvey-Ras gene in psychiatric disorders (1996) (45)
Replicative heterogeneity of mammalian DNA. (1972) (45)
The gene-immune-behavioral pathway: Gamma-interferon (IFN-γ) simultaneously coordinates susceptibility to infectious disease and harm avoidance behaviors (2014) (44)
DNA-binding properties of nuclear matrix proteins. (1978) (43)
Hereditary Agoraphobia and Obsessive-Compulsive Behaviour in Relatives of Patients with Gilles de la Tourette's Syndrome (1987) (43)
Tourette's syndrome and attention deficit disorder with hyperactivity. (1987) (43)
Mutation screening of the dopamine D1 receptor gene in Tourette's syndrome and alcohol dependent patients. (1998) (43)
Mechanisms of chromosome banding (2004) (42)
A controlled family history study of Tourette's syndrome, III: Affective and other disorders. (1990) (42)
Neurogenetic interactions and aberrant behavioral co-morbidity of attention deficit hyperactivity disorder (ADHD): dispelling myths (2005) (41)
A multigene test for the risk of sporadic breast carcinoma (2003) (41)
A “line item” approach to the identification of genes involved in polygenic behavioral disorders: The Adrenergic α2A (ADRA2A) gene (2003) (41)
Sex chromatin, nuclear size and the cell cycle. (1967) (39)
Association of the acid phosphatase (ACP1) gene with triglyceride levels in obese women. (2002) (38)
Nuclear proteins. IV. Deficiency of non-histone proteins in condensed chromatin of Drosophila virilis and mouse. (1977) (38)
Phenylethanolamine N-methyltransferase G-148A genetic variant and weight loss in obese women. (2003) (38)
Alternative hypotheses on the inheritance of Tourette syndrome. (1992) (38)
Fine structure of the synaptonemal complex. Regular and stereo electron microscopy of deoxyribonuclease-treated whole mount preparations. (1971) (37)
Role of genetic factors in human sexual behavior based on studies of Tourette syndrome and ADHD probands and their relatives. (1994) (37)
Conradi's disease. Chondrodystrophia calcificans congenita, congenital stippled epiphyses. (1968) (37)
Tourette's syndrome and homozygosity for the dopamine D3 receptor gene (1993) (35)
No association of a tyrosine hydroxylase gene tetranucleotide repeat polymorphism in autism, Tourette syndrome, or ADHD (1995) (35)
Methylation of euchromatic and heterochromatic DNA. (1972) (34)
Two-dimensional gel electrophoresis of human brain proteins. III. Genetic and non-genetic variations in 145 brains. (1982) (34)
Association of CCR5 Δ32 deletion with early death in multiple sclerosis (2004) (34)
The Kleeblattschdel syndrome—agrotesque form of hydrocephalus (1965) (34)
Chromosome banding. (1975) (34)
A controlled family history study of Tourette's syndrome, II: Alcoholism, drug abuse, and obesity. (1990) (33)
Tourette's syndrome: a behavioral spectrum disorder. (1995) (33)
Interaction between infectious diseases and personality traits: ACP1*C as a potential mediator. (2014) (32)
Two-dimensional gel electrophoresis of human brain proteins. I. Technique and nomenclature of proteins. (1982) (32)
Mechanisms of chromosome banding. VI. Whole mount electron microscopy of banded metaphase chromosomes and a comparison with pachytene chromosomes. (1975) (30)
Fibroblasts in Huntington's disease. (1975) (30)
Two-dimensional gel electrophoresis of human brain proteins. IV. Disorders of glial proliferation and a polymorphism of glial fibrillary acidic protein--GFAP Duarte. (1982) (30)
Genetic aspects of childhood behavioral disorders (1997) (30)
A dopamine D3 receptor genotype is associated with hyperandrogenic chronic anovulation and resistant to ovulation induction with clomiphene citrate in female Hispanics. (1995) (29)
Autosomal dominant insensitivity to pain with hyperplastic myelinopathy and autosomal dominant indifference to pain (1974) (29)
Association of CCR5 delta32 deletion with early death in multiple sclerosis. (2004) (28)
A case of familial exhibitionism in Tourette's syndrome successfully treated with haloperidol. (1982) (27)
Chinese hamster nuclear proteins. An electrophoretic analysis of interphase, metaphase and nuclear matrix preparations. (1982) (27)
Two-dimensional gel electrophoresis of human brain proteins. V. Non-equilibrium gel electrophoresis, with detection of a myelin basic protein mutation--MBL-Duarte. (1982) (27)
Some aspects of chromosome structure in eukaryotes. (1974) (27)
Mechanisms of chromosome banding (1978) (26)
HEREDITARY LOCALIZED PRURITUS. (1965) (26)
Red blood cell choline in Tourette syndrome. (1982) (25)
URIDINE-5-H3 RADIOAUTOGRAPHY OF THE HUMAN SEX CHROMATIN BODY (1966) (25)
A controlled study of Tourette syndrome-Revisited: A reply to the letter of Pauls et al. (1988) (25)
Tourette's syndrome and attention-deficit hyperactivity disorder: evidence for a genetic relationship. (1993) (24)
DNA loss during Robertsonian fusion in studies of the tobacco mouse. (1972) (24)
Genetic Influences on Childbearing Motivation: Further Testing a Theoretical Framework (2000) (24)
Evidence for an X-linked modifier gene affecting the expression of Tourette syndrome and its relevance to the increased frequency of speech, cognitive, and behavioral disorders in males. (1986) (23)
Preliminary association of both the Dopamine D2 Receptor (DRD2) (Taq1 A1 Allele) and the Dopamine Transporter (DAT1) (480 bp Allele) genes with pathological aggressive behavior, a clinical subtype of Reward Deficiency Syndrome (RDS) in adolescents (2007) (23)
Fine structure of the heterochromatin of the kangaroo rat Dipidomys ordii, and examination of the possible role of actin and myosin in heterochromatin condensation. (1976) (23)
13 – Compartmentalization of Nuclear and Chromatin Proteins (1978) (23)
Huntington disease and Tourette syndrome. I. Electron spin resonance of bed ghosts. (1981) (22)
Sister chromatid exchange and chromosome organization based on a bromodeoxyuridine Giemsa-C-banding technique (TC-Banding) (1975) (22)
Principles and practice of medical genetics (1984) (22)
Whole mount electron microscopy of metaphase. I. Chromosomes and microtubules from mouse oocytes. (1972) (22)
Do the Giemsa-banding patterns of chromosomes change during embryonic development? (1972) (22)
An examination of the association between DRD4 and DRD2 polymorphisms and personality traits (2002) (22)
Presidential address: the genetics of human behavior--lessons for two societies. (1989) (21)
Mechanisms of chromosome banding. IV. Optical properties of the Giemsa dyes. (1975) (21)
Two-dimensional gel electrophoresis of human brain proteins. II. Specific proteins and brain subfractions. (1982) (21)
Nuclear proteins. VI. Fractionation of chromosomal non-histone proteins using hydrophobic chromatography. (1979) (21)
HLA typing in Tourette syndrome. (1982) (21)
Role of genetic factors in depression based on studies of Tourette syndrome and ADHD probands and their relatives. (1995) (21)
Absence of Cis Delta Chain Synthesis in (δ β) Thalassemia (F-thalassemia) (1966) (21)
Association between the phenylethanolamine N-methyltransferase gene and multiple sclerosis (2002) (21)
H3-uridine autoradiography of human chromosomes. (1966) (21)
Genetic influences on childbearing motivation: a theoretical framework and some empirical evidence. (1999) (20)
Association of dopamine D2 receptor gene haplotypes with anovulation and fecundity in female Hispanics. (1994) (20)
Chromosome organization. (1976) (20)
Mechanisms of chromosome banding (1976) (20)
Replication of repetitious DNA and the S period. (1970) (20)
Lymphocyte transformation in response to phytohemagglutinin during and following a pregnancy. (1967) (20)
Implications of somatic recombination and sister chromatid exchange in Bloom's syndrome and cells treated with mitomycin C (1975) (19)
ORIGINAL RESEARCH ARTICLE Studies of the potential role of the dopamine D 1 receptor gene in addictive behaviors (1997) (19)
Partial albinism. (1966) (19)
The LEP gene and age of menarche: maternal age as a potential cause of hidden stratification in association studies. (2001) (18)
Association Between the γ-Aminobutyric Acid A3 Receptor Gene and Multiple Sclerosis (1998) (18)
Obstructing Aspergillus cast of the renal pelvis. Report of a case in a patient having diabetes mellitus and Addison's disease. (1962) (18)
TS, learning, and speech problems. (1994) (18)
Isolabelling and chromosome strandedness. (1971) (17)
Genetic factors in substance abuse based on studies of Tourette syndrome and ADHD probands and relatives. II. Alcohol abuse. (1994) (17)
Huntington disease and Tourette syndrome. II. Uptake of glutamic acid and other amino acids by fibroblasts. (1981) (17)
Studies of microchromosomes and a G-C rich DNA satellite in the quail (2004) (17)
GSK3β genetic variability in patients with Multiple Sclerosis (2011) (17)
Whole mount electron microscopy of human meiotic chromosomes. (1971) (16)
MYELOBLASTOMA PRECEDING BLOOD AND MARROW EVIDENCE OF ACUTE LEUKEMIA. (1965) (16)
Histones and G banding of chromosomes. (1976) (16)
Do half-chromatids exist? (1970) (16)
The Gene Bomb: Does Higher Education and Advanced Technology Accelerate the Selection of Genes for Learning Disorders, Adhd, Addictive, and Disruptive Behaviors? (1996) (16)
Chromium Picolinate (CrP) a putative anti-obesity nutrient induces changes in body composition as a function of the Taq1 dopamine D2 receptor polymorphisms in a randomized double-blind placebo controlled study (2007) (15)
The clonidine patch and behavior problems. (1990) (15)
Centromere: Absence of DNA Replication during Chromatid Separation in Human Fibroblasts (1966) (14)
Association between the low molecular weight cytosolic acid phosphatase gene ACP1*A and comorbid features of Tourette syndrome (2002) (14)
Reverse banding of Japanese quail microchromosomes. (1976) (14)
The Dopamine D2 Receptor Gene (DRD2) and Neuropsychiatric Disorders (1994) (14)
Reviewing the role of putative candidate genes in "Neurobesigenics," a clinical subtype of Reward Deficiency Syndrome (RDS) (2007) (14)
The real problem in association studies (2003) (13)
Association between the estrogen receptor TA polymorphism and Harm avoidance (2009) (13)
Cytoplasmic DNA-binding proteins. (1973) (13)
Attention-de fi cit-hyperactivity disorder and reward de fi ciency syndrome (2008) (13)
11 – The Structure of Human Chromosomes (1974) (13)
Candidate genes and association studies in psychiatry. (1994) (12)
Quantitative autoradiography of heterochromatin replication in Microtus agrestis (2004) (12)
DSM-IV criteria for Tourette's. (1995) (11)
3 – Two-Dimensional Gel Electrophoresis of Nuclear Particles (1981) (11)
Prenatal diagnosis and the "New genetics.". (1980) (11)
Benign symmetric lipomatosis. (1968) (11)
Chapter 11 Methods and Mechanisms of Chromosome Banding (1978) (10)
Half-chromatid aberrations and chromosome strandedness. (1970) (10)
Anisotropic lipids and urinary cholesterol excretion. (1963) (10)
The Gene Bomb (1997) (9)
Evidence that heavy shoulder DNA may be localized to the microchromosomes of birds. (1972) (9)
Evidence of an Emerging Collision Between the Fertility Transition and Genotype-Dependent Fertility Differentials (2003) (9)
Molecular genetic prenatal determination of twin zygosity. (1988) (8)
The distribution of sister chromatids at mitosis in Chinese hamster cells (2004) (8)
Genetic factors in drug abuse and dependence. (1996) (8)
Molecular heterosis Implications for complex inheritance (1997) (8)
Idiopathic paroxysmal myoglobinuria. (1961) (8)
THE KLEEBLATTSCHAEDE SYNDROME--A GROTESQUE FORM OF HYDROCEPHALUS. (1965) (7)
Serotonin and the biochemical genetics of alcoholism: lessons from studies of attention deficit hyperactivity disorder (ADHD) and Tourette syndrome. (1993) (7)
SYMPHALANGISM AND FOURTH DIGIT HYPOPHALANGISM. (1965) (7)
Thermal denaturation of DNA and chromatin of early and late passage human fibroblasts. (1971) (7)
Isolation of a non-histone chromosomal high mobility group protein from mouse liver nuclei by hydrophobic chromatography. (1981) (7)
Genetic aspects of speech and language disorders (1984) (7)
Tourette's syndrome and psychiatric disorders (1995) (7)
Myxedema with Erb's limb girdle muscular dystrophy. Report of a case with a review of the muscular abnormalities of myxedema. (1962) (7)
The D2 Dopamine Receptor and Tourette's Syndrome-Reply (1992) (7)
New frontiers in genetic medicine. (1986) (7)
Two-dimensional gel electrophoresis of 125I-labeled surface proteins of human fibroblasts. (1979) (7)
Both Genes and Environment Play a Role in Antisocial Behavior (1996) (6)
Age at First Childbirth: A Major Selective Factor for Psychiatric Genes in the Twentieth Century (2000) (6)
Substitution of polybuffer for ampholytes in isoelectric focusing. (1982) (6)
Normal two-dimensional gel electrophoresis of alpha-2-macroglobulin in cystic fibrosis. (1980) (6)
Familial Multifocal Fibrosclerosis (2020) (6)
A THIRD γ-GLOBULIN CHAIN ? (1963) (6)
Single Amino-acid Substitutions as a Result of Unequal Crossing-over (1966) (6)
Polygenic inheritance and minisatellites (1996) (6)
Studies of human germinal mutations by deoxyribonucleic acid hybridization. (1989) (6)
109-5 Association of polymorphisms of dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes with schizoid/avoidant behaviors (SAB) and pathological violence (PV) (1997) (6)
The Genetics of Tourette Syndrome and its Relationship to Other Psychiatric Disorders (1989) (5)
SNPs and polygenic disorders: a less gloomy view (1999) (5)
Absence of cis delta chain synthesis in (sigma beta) thalassemia (F-thalassemia). (1966) (5)
Superiority of lyophilization over sodium dodecyl sulfate (SDS) in the preservation of chromatin for electrophoresis. (1975) (5)
Sexual abuse or Tourette syndrome? (1993) (5)
Specific interaction between mouse liver non-histone chromosomal proteins and mouse DNA demonstrated by a sequential DNA-protein binding procedure. (1978) (5)
Heavy shoulder DNA in snakes. (1973) (5)
Structure of mammalian chromosomes. (1974) (5)
Modulation of a number of genes on personality traits in a sample of healthy subjects (2014) (5)
Association between the gamma-aminobutyric acid A3 receptor gene and multiple sclerosis. (1998) (5)
SIDS and tourette syndrome: Is there an etiologic relationship? (1993) (4)
Monoamine oxidase gene variants in Tourette syndrome (1996) (4)
Two-Dimensional Gel Electrophoresis of Human Brain Proteins. Part V (1982) (4)
GENETIC HETEROGENEITY OF HUMAN BRAIN PROTEINS AND THEIR DIAGNOSIS IN LIVING PATIENTS (1982) (4)
Nuclear proteins. V. Studies of histone-binding proteins from mouse liver by affinity chromatography. (1978) (4)
Model for Evolutionary Origin of Chromosome Bands (1973) (4)
Methods and mechanisms of chromosome banding. (1978) (4)
Attention-defi cit-hyperactivity disorder and reward defi ciency syndrome (2008) (3)
Dopamine D2 receptor and Tourette's syndrome. (1995) (3)
Heavy shoulder DNA. (1972) (3)
Psychology Autosomal dominant insensitivity to pain with hyperplastic myelinopathy and dominant indifference to painNeurology (Minneap.), 24 (1974) 838–848 (1976) (3)
The Neurobiology, Genetics and Evolution of Human Spirituality The Central Role of the Temporal Lobes (2010) (3)
Mechanisms of chromosome banding. XI. The ability of various acridine derivatives to cause Q-banding. (1978) (3)
Triple-spot proteins in two-dimensional gel electrophoresis. (1979) (3)
A note on experimental approaches to Huntington's disease. (1976) (2)
Genetic analysis of the X chromosome—Studies of duchenne muscular dystrophy and related disorders. (1983) (2)
Dopamine D1 receptor gene and addictive behaviors (1996) (2)
Input from Our Readers (1999) (2)
Polygenes associated with intravenous drug use (1996) (2)
DOPAMINE D2 RECEPTOR (DRD2) HAPLOTYPE STATUS AND GENETIC RISK FOR ALCOHOLISM AND POLYSUBSTANCE ABUSE (1992) (2)
Clinical and genetic relationships between autism--pervasive developmental disorder and Tourette Syndrome. A study of 19 cases (1995) (2)
Role of the HTR1A serotonin receptor gene in Tourette syndrome and conduct disorder (1996) (2)
Richard M. Goodman, M.D. (1991) (1)
Comparison of meralluride with a new oral diuretic. (1963) (1)
Molecular human cytogenetics (1977) (1)
Association of OB gene with obesity, depression and anxiety in young women (1996) (1)
Gene products of Amphiuma: An amphibian with an excessive amount of DNA (2005) (1)
Hereditary localized pruritus. (1965) (1)
Molecular structure of the number 21 chromosome and Down syndrome (1986) (1)
22% of preschool children, 8% of primary school students and 3% of adolescents have tics (2003) (1)
Obstructing aspergillus case to the renal pelvis. Report of a case in a patient having diabetes mellitus and Addison's disease. (1962) (1)
Homozygosity for Pc 1 Duarte-like protein in primates and other animals. (1981) (1)
Lateral asymmetry of human chromosomes. (1978) (1)
THE D2 DOPAMINE RECEPTOR AND TOURETTE'S SYNDROME. AUTHOR'S REPLY (1992) (1)
Mendelian inheritance in man (1979) (1)
A General Theory of Carcinogenesis ( genes / viruses ) (1)
S.10.02 Genetics of pathological gambling and substance use disorders (2006) (1)
109-4 Different genes for susceptibility to drug versus alcohol dependence (1997) (1)
Clinical genetics. A source book for physicians (1980) (1)
Two-dimensional Gel Electrophoresis of Rat Liver Nuclear Washes , Nuclear Matrix , and h n RNA Proteins (1)
Associations Between the Endothelial Nitric Oxide Synthase Gene (NOS3), Reproductive Behaviors, and Twinning (2000) (1)
The ups and downs of Huntington disease research. (1981) (1)
Examination of human brain proteins by two-dimensional gel electrophoresis. (1982) (1)
Relationship of the GABRB3 gene to adult ADHD and personality traits in Caucasian and African-American samples (1996) (1)
Association Between the g-Aminobutyric Acid A3 Receptor Gene and Multiple Sclerosis (2000) (1)
Planning for a healthy baby: A guide to genetic and environmental risks (1986) (1)
The hereditary ataxias and related disorders (1985) (1)
CANCER AND DERMATOGLYPHICS (1968) (1)
Genes and the mind: Inheritance of mentall illness (1981) (0)
An association between the neuronal nitric oxide synthase gene (nNOS1a) and aggressive/addictive behavior (1996) (0)
Maternal age as a potential explanation of the role of the L allele of the serotonin transporter gene in anxiety and depression in Asians (2014) (0)
Chromosome structure and chromosome banding. (1976) (0)
Editorial help (2004) (0)
Genetics of the brain (1983) (0)
Clinodactyly deformity simulating trisomy-18 hand malformation. (1970) (0)
Subject Index Vol. 9, 1970 (2004) (0)
The Genetics of Neurological Disorders (1967) (0)
Spontaneous genomic instability in humans: Final report (1989) (0)
Nonhistone proteins and chromosome structure. (1980) (0)
Is the Nuclear Membrane Involved in DNA Replication (1974) (0)
Brief Review: Increasing the Variance for Genes in RDS and Other Polygenic Disorders (2016) (0)
Maternal age as a potential explanation of the role of the L allele of the serotonin transporter gene in anxiety and depression in Asians (2014) (0)
Powerful new tools in genetics. (1979) (0)
Behaviour Genetics – Human (2002) (0)
The biochemical genetics of man (1979) (0)
Our Readers and Contributors. (0)
Associations between the 5HT-2R gene and psychiatric symptoms in substance abusers and controls (1996) (0)
Congenital and acquired cognitive disorders (1979) (0)
Miscellaneous: SEX CHROMATIN, NUCLEAR SIZE AND THE CELL CYCLE (1967) (0)
Comings replies (1998) (0)
Book Review Index Vol. 9, 1970 (1970) (0)
Symposia presented at the American Society of Human Genetics annual meeting, Portland, October 16–19, 1974: The X chromosome: A quarter century later. (1975) (0)
An association between the dopamine-β-hydroxylase dinucleotide repeat polymorphism and drug abuse patterns (1996) (0)
Practical genetic counselling (1982) (0)
Crush artifact may cloud electronmicroscopy (1975) (0)
Behavioral genetics —A primer (1980) (0)
Cannabinoid receptor gene (CBI) association with ERP P300 wave amplitude and drug dependence (1996) (0)
Response to letter by William H. James. (1995) (0)
Huntington's Chorea (1954) (0)
THE SPHERE OF INFLUENCE OF THE BETA-THALASSEMIA MUTATION. (1963) (0)
Genetic engineering. (1983) (0)
Psychology (1976) (0)
Malformations in children from one to seven years (1986) (0)
Beyond the lack of association between IFNG +874T>A polymorphism and personality traits in healthy Japanese subjects: Possible ethnic-specific effects (2016) (0)
Color atlas of clinical genetics. (1984) (0)

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