Lillian Lockhart, MD

  • 788 Citations
  • 16 h-Index
1964 …2011

Research output per year

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Research Output

  • 788 Citations
  • 16 h-Index
  • 45 Article
  • 4 Letter
  • 1 Editorial
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Article
2011

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia

Northup, J. K., Matalon, R., Lockhart, L. H., Hawkins, J. C. & Velagaleti, G. V. N., Jul 1 2011, In : European Journal of Medical Genetics. 54, 4, p. e394-e398

Research output: Contribution to journalArticle

3 Scopus citations
2008

Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement

Cooke, S. L., Northup, J. K., Champaige, N. L., Zinser, W., Edwards, P. A. W., Lockhart, L. H. & Velagaleti, G. V. N., May 1 2008, In : American Journal of Medical Genetics, Part A. 146, 9, p. 1166-1172 7 p.

Research output: Contribution to journalArticle

11 Scopus citations

Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family

Velagaleti, G. V. N., Hawkins, J. C., Panova, N. I. & Lockhart, L. H., Sep 1 2008, In : Indian Journal of Pediatrics. 75, 9, p. 956-960 5 p.

Research output: Contribution to journalArticle

2 Scopus citations
2007

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

Northup, J. K., Gadre, S. A., Ge, Y., Lockhart, L. H. & Velagaleti, G. V. N., Feb 1 2007, In : European Journal of Haematology. 78, 2, p. 152-156 5 p.

Research output: Contribution to journalArticle

7 Scopus citations

Unusual pseudo dicentric, psu dic (1;19)(q10;q13.42), in a female with premature ovarian failure

Northup, J., Griffis, K., Hawkins, J., Lockhart, L. & Velagaleti, G., Mar 2007, In : Fertility and Sterility. 87, 3, p. 697.e5-697.e8

Research output: Contribution to journalArticle

7 Scopus citations
2005

Position effects due to chromosome breakpoints that map ∼900 Kb upstream and ∼1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia

Velagaleti, G. V. N., Bien-Willner, G. A., Northup, J. K., Lockhart, L. H., Hawkins, J. C., Jalal, S. M., Withers, M., Lupski, J. R. & Stankiewicz, P., Apr 2005, In : American Journal of Human Genetics. 76, 4, p. 652-662 11 p.

Research output: Contribution to journalArticle

136 Scopus citations

Subtelomeric rearrangements in idiopathic mental retardation

Velagaleti, G. V. N., Robinson, S. S., Rouse, B. M., Tonk, V. S. & Lockhart, L. H., Aug 2005, In : Indian Journal of Pediatrics. 72, 8, p. 679-685 7 p.

Research output: Contribution to journalArticle

11 Scopus citations
2004

Molecular Cytogenetic Characterization of a Recombinant Chromosome rec(22)dup(22q)inv(22)(p13q12.2)

Tonk, V. S., Jesurun, C. A., Morgan, D. L., Lockhart, L. H. & Velagaleti, G. V. N., Jan 1 2004, In : American Journal of Medical Genetics. 124 A, 1, p. 92-95 4 p.

Research output: Contribution to journalArticle

2 Scopus citations
2003

A Rapid and Noninvasive Method for Detecting Tissue-Limited Mosaicism: Detection of i(12)(p10) in Buccal Smear from a Child with Pallister-Killian Syndrome

Velagaleti, G. V. N., Tapper, J. K., Rampy, B. A., Zhang, S., Hawkins, J. C. & Lockhart, L. H., Sep 1 2003, In : Genetic Testing. 7, 3, p. 219-223 5 p.

Research output: Contribution to journalArticle

20 Scopus citations

Disease associated balanced chromosome rearrangements (DBCR): Report of two new cases

Tonk, V. S., Wyandt, H. E., Huang, X., Patel, N., Morgan, D. L., Kukolich, M., Lockhart, L. H. & Velagaleti, G. V. N., Jan 1 2003, In : Annales de Genetique. 46, 1, p. 37-43 7 p.

Research output: Contribution to journalArticle

8 Scopus citations

Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25→qter and monosomy 18p11.3→pter in a girl with dysmorphic features

Velagaleti, G. V. N., Jalal, S. M., Michaelis, R. C., Rowe, T. F., Nichols, J. R. & Lockhart, L. H., Jan 1 2003, In : Clinical Dysmorphology. 12, 1, p. 29-33 5 p.

Research output: Contribution to journalArticle

6 Scopus citations
2002

Chromosome 13q neocentromeres: Molecular cytogenetic characterization of three additional cases and clinical spectrum

Li, S., Malafiej, P., Levy, B., Mahmood, R., Field, M., Hughes, T., Lockhart, L. H., Wu, Z., Huang, M., Hirschhorn, K., Velagaleti, G. V. N., Daniel, A. & Warburton, P. E., Jul 1 2002, In : American Journal of Medical Genetics. 110, 3, p. 258-267 10 p.

Research output: Contribution to journalArticle

22 Scopus citations

De novo supernumerary ring chromosome 7: First report of a non-mosaic patient and review of the literature

Velagaleti, G. V. N., Jalal, S. M., Kukolich, M. K., Lockhart, L. H. & Tonk, V. S., Mar 1 2002, In : Clinical Genetics. 61, 3, p. 202-206 5 p.

Research output: Contribution to journalArticle

16 Scopus citations

Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes

Tapper, J. K., Zhang, S., Harirah, H. M., Panova, N. I., Merryman, L. S., Hawkins, J. C., Lockhart, L. H., Gei, A. B. & Velagaleti, G. V. N., Dec 1 2002, In : Fetal Diagnosis and Therapy. 17, 6, p. 347-351 5 p.

Research output: Contribution to journalArticle

17 Scopus citations

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay

Levy, B., Jalal, S. M., Dunn, T. M., Warburton, P. E., Tonk, V. S., Hirschhorn, K., Lockhart, L. H., Hughes, T. & Velagaleti, G. V. N., Mar 15 2002, In : American Journal of Medical Genetics. 108, 3, p. 198-204 7 p.

Research output: Contribution to journalArticle

8 Scopus citations
2001

Trisomy 4 pter-q12 and monosomy of chromosome 13 pter-q12 in a male with deficiency of all blood lymphocyte populations

Velagaleti, G. V. N., Lockhart, L. H., Schmalstieg, F. C. & Goldman, A. S., Aug 1 2001, In : American Journal of Medical Genetics. 102, 2, p. 139-145 7 p.

Research output: Contribution to journalArticle

1 Scopus citations
2000

Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndrome

Velagaleti, G. V. N., Kumar, A., Lockhart, L. H. & Matalon, R., Jan 1 2000, In : Annales de Genetique. 43, 2, p. 105-107 3 p.

Research output: Contribution to journalArticle

11 Scopus citations
1999

Pregnancy in bone marrow failure syndromes: Diamond-Blackfan anaemia and Shwachman-Diamond syndrome

Alter, B. P., Kumar, M., Lockhart, L. L., Sprinz, P. G. & Rowe, T. F., Nov 6 1999, In : British Journal of Haematology. 107, 1, p. 49-54 6 p.

Research output: Contribution to journalArticle

22 Scopus citations
1990

Genetic services for underserved populations. B. Needs assessment: Identifying the underserved: Needs assessment for genetic services in Texas

McCabe, E. R. B., Patterson, P. J., Botsonis, H., Day, D. W., Lockhart, L., Martinec, J. D., Weber, B., Godbout, R. & Malitz, D., Sep 28 1990, In : Birth Defects: Original Article Series. 26, 2, p. 54-58 5 p.

Research output: Contribution to journalArticle

1 Scopus citations

Genetic services for underserved populations. C. Finance/insurance issues: A study of medical costs associated with selected genetic disorders in Texas

McCabe, E. R. B., Patterson, P. J., Botsonis, H., Day, D. W., Lockhart, L., Martinec, J. D., Weber, B., Godbout, R. & Malitz, D., Sep 28 1990, In : Birth Defects: Original Article Series. 26, 2, p. 132-138 7 p.

Research output: Contribution to journalArticle

Maternal phenylketonuria pregnancy outcome: a preliminary report of facial dysmorphology and major malformations

Rouse, B., Lockhart, L., Matalon, R., Azen, C., Koch, R., Hanley, W., Levy, H., dela Cruz, F. & Friedman, E., May 1 1990, In : Journal of Inherited Metabolic Disease. 13, 3, p. 289-291 3 p.

Research output: Contribution to journalArticle

36 Scopus citations
1989

Trisomy 18 and hepatoblastoma

Mamlok, V., Nichols, M., Lockhart, L. & Mamlok, R., Jan 1 1989, In : American Journal of Medical Genetics. 33, 1, p. 125-126 2 p.

Research output: Contribution to journalArticle

24 Scopus citations
1988

Cornelia de Lange syndrome with Peters anomaly and fat malabsorption

Ponder, S. W., Cynamon, H. A., Isenberg, J. N., Elder, F. F. B. & Lockhart, L., Jan 1 1988, In : Dysmorphology and Clinical Genetics. 2, 1, p. 2-5 4 p.

Research output: Contribution to journalArticle

4 Scopus citations
1986

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17

Greenberg, F., Stratton, R. F., Lockhart, L. H., Elder, F. F., Dobyns, W. B. & Ledbetter, D. H., Jan 1 1986, In : American Journal of Medical Genetics. 23, 4, p. 853-859 7 p.

Research output: Contribution to journalArticle

20 Scopus citations

Proximal duplications of chromosome 15: clinical dilemmas

Hood, O. J., Rouse, B. M., Lockhart, L. H. & Bodensteiner, J. B., Mar 1986, In : Clinical Genetics. 29, 3, p. 234-240 7 p.

Research output: Contribution to journalArticle

7 Scopus citations
1984

Familial autism and the fragile-X chromosome

August, G. J. & Lockhart, L. H., Jun 1 1984, In : Journal of Autism and Developmental Disorders. 14, 2, p. 197-204 8 p.

Research output: Contribution to journalArticle

13 Scopus citations

Identical twins with deletion 16q syndrome: Evidence that 16q12.2-q13 is the critical band region

Elder, F. F. B., Ferguson, J. W. & Lockhart, L. H., Jul 1 1984, In : Human Genetics. 67, 2, p. 233-236 4 p.

Research output: Contribution to journalArticle

16 Scopus citations
1981

A Care-by-Parent Unit: Its Planning, Implementation and Patient Satisfaction

Caldwell, B. S. & Lockhart, L. H., Jun 1 1981, In : Children's Health Care. 10, 1, p. 4-7 4 p.

Research output: Contribution to journalArticle

5 Scopus citations
1980

Observations on prostaglandins in normal and leukemic human lymphocytes

Carpentieri, U., Brouhard, B. H., LaGrone, L. & Lockhart, L. H., Jan 1 1980, In : Prostaglandins. 20, 6, p. 1117-1129 13 p.

Research output: Contribution to journalArticle

4 Scopus citations
1979

Nonrandom distribution of chromosomal aberrations induced by three chemicals

Meyne, J., Lockhart, L. H. & Arrighi, F. E., Nov 1979, In : Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 63, 1, p. 201-209 9 p.

Research output: Contribution to journalArticle

48 Scopus citations

Quantitative analysis and discussion of Mexican and Anglo-Americans' response to intervention in genetic disease

Naranjo, M. S. F. & Lockhart, L. H., Dec 1 1979, In : Birth Defects: Original Article Series. 15, 5 C, p. 267-280 14 p.

Research output: Contribution to journalArticle

1978

Clinical experience in prevention of candidiasis by nystatin in children with acute lymphocytic leukemia

Carpentieri, U., Haggard, M. E., Lockhart, L. H., Gustavson, L. P., Box, Q. T. & West, E. F., Apr 1978, In : The Journal of Pediatrics. 92, 4, p. 593-595 3 p.

Research output: Contribution to journalArticle

35 Scopus citations

Cytogenetic effects of cis-platinum(II)diamminedichloride on human lymphocyte cultures

Meyne, J. & Lockhart, L. H., Sep 1978, In : Mutation Research/Genetic Toxicology. 58, 1, p. 87-97 11 p.

Research output: Contribution to journalArticle

34 Scopus citations

Immunohemolytic anemia in children: a review. Part I.

Carpentieri, U., Haggard, M. E., Gustavson, L. P. & Lockhart, L. H., Sep 1 1978, In : Texas medicine. 74, 9, p. 43-50 8 p.

Research output: Contribution to journalArticle

1974

Acquired hypothyroidismwith muscular hypertrophy and precocious testicular enlargement

Hopwood, N. J., Lockhart, L. H. & Bryan, G. T., Aug 1974, In : The Journal of Pediatrics. 85, 2, p. 233-236 4 p.

Research output: Contribution to journalArticle

8 Scopus citations
1973

Assay for detection of the cystic fibrosis gene

Lockhart, L. H. & Bowman, B. H., Dec 1 1973, In : Texas reports on biology and medicine. 31, 4, p. 631-638 8 p.

Research output: Contribution to journalArticle

8 Scopus citations

Cystic fibrosis: growth kinetics and production of the ciliary inhibitor by cultured fibroblasts

Barnett, D. R., Barranco, S. C., Lockhart, L. H., Lankford, B. J., Meyne, J. & Bowman, B. H., Dec 1 1973, In : Texas reports on biology and medicine. 31, 4, p. 691-696 6 p.

Research output: Contribution to journalArticle

3 Scopus citations

Cystic fibrosis: Synthesis of ciliary inhibitor by amniotic cells

Bowman, B. H., Lockhart, L. H., Herzberg, V. L., Barnett, D. R., Armstrong, D. & Kramer, J., Nov 1973, In : Clinical Genetics. 4, 6, p. 461-463 3 p.

Research output: Contribution to journalArticle

9 Scopus citations
1972

Congenital idiopathic hypertrophic subaortic stenosis associated with a phenotypic Turner's syndrome

Nghiem, Q. X., Toledo, J. R., Schreiber, M. H., Harris, L. C., Lockhart, L. L. & Tyson, K. R. T., Nov 8 1972, In : The American Journal of Cardiology. 30, 6, p. 683-689 7 p.

Research output: Contribution to journalArticle

7 Scopus citations
1970

Cystic fibrosis: Characterization of the inhibitor to ciliary action in oyster gills

Bowman, B. H., McCombs, M. L. & Lockhart, L. H., Jan 1 1970, In : Science. 167, 3919, p. 871-873 3 p.

Research output: Contribution to journalArticle

46 Scopus citations
1969

Oyster ciliary inhibition by cystic fibrosis factor

Bowman, B. H., Lockhart, L. H. & McCombs, M. L., Jan 1 1969, In : Science. 164, 3877, p. 325-326 2 p.

Research output: Contribution to journalArticle

94 Scopus citations
1968

Chromosomes of the sterile hybrid duck

Mott, C. L., Lockhart, L. H. & Rigdon, R. H., Jan 1 1968, In : Cytogenetic and Genome Research. 7, 5, p. 403-412 10 p.

Research output: Contribution to journalArticle

14 Scopus citations
1967
18 Scopus citations
1965

THE BEGINNING AND THE TERMINAL STAGES OF DNA SYNTHESIS OF HUMAN CELLS WITH AN XXXXY CONSTITUTION

HSU, T. C. & LOCKHART, LILLIAN. H., Mar 1965, In : Hereditas. 52, 3, p. 320-324 5 p.

Research output: Contribution to journalArticle

Open Access
10 Scopus citations
1964

CYTOGENETIC STUDIES. DIAGNOSTIC TOOL IN CLINICAL MEDICINE.

ROUSE, B. M., LOCKHART, L. H. & HAGGARD, M. E., Aug 1 1964, In : Texas medicine. 60, p. 642-649 8 p.

Research output: Contribution to journalArticle