D. Wellesley

Details der Publikationsliste

Zeitraum

2003 - 2009

Anzahl

36

Co-Autoren

Ambient Air Pollution and Risk of Congenital Anomalies in England, 1991-99 (2009)

Dolk, H., Armstrong, B., Lachowycz, K., Vrijheid, M., Rankin, J., Abramsky, L., ...

OBJECTIVES: To investigate whether there is an association between risk of congenital anomaly and annual ward level exposure to air pollution in England during the 1990s. METHODS: A geographical...

Does lamotrigine use in pregnancy increase orofacial cleft risk relative to other malformations? (2009)

Dolk, H., Jentink, J., Loane, M., Morris, J., De Jong-van Den Berg, L.T., Calzolari, E., ...

Objective: to investigate whether first trimester exposure to lamotrigine (LTG) monotherapy is specifically associated with an increased risk of orofacial clefts (OCs) relative to other...

Parental attitude to participating in long-term follow up studies of their children's health after in utero diagnosis of abnormalities (2009)

Ramsay, L., Howe, D.T., Wellesley, D.

Objective: To determine whether parents might be distressed if approached to take part in long-term follow-up of their children's health and development. Methods: A short, closed format anonymous...

Parental attitude to participating in long-term follow-up studies of their children’s health after in utero diagnosis of abnormalities (2009)

Ramsay, L., Howe, D.T., Wellesley, D.

Objective To determine whether parents might be distressed if approached to take part in long-term follow-up of their children's health and development. Methods A short, closed format anonymous...

The hidden mortality of transposition of the great arteries and survival advantage provided by prenatal diagnosis (2008)

Blyth, M., Howe, D., Gnanapragasam, J., Wellesley, D.

Objective To describe the sensitivity of fetal anomaly scanning at detecting transposition of the great arteries (TGA) and to investigate whether prenatal detection improves survival. Design...

The hidden mortality of transposition of the great arteries and survival advantage provided by prenatal diagnosis (2008)

Blyth, M., Howe, D., Gnanapragasam, J., Wellesley, D.

OBJECTIVE: To describe the sensitivity of fetal anomaly scanning at detecting transposition of the great arteries (TGA) and to investigate whether prenatal detection improves survival. DESIGN:...

Geographic variation and localised clustering of congenital anomalies in Great Britain (2007)

Armstrong, B.G., Dolk, H., Pattenden, S., Vrijheid, M., Loane, M., Rankin, J., ...

Background Environmental pollution as a cause of congenital anomalies is sometimes suspected because of clustering of anomalies in areas of higher exposure. This highlights questions around spatial...

Prevalence of congenital anomalies in five British regions, 1991-99 (2005)

Rankin, J., Pattenden, S., Abramsky, L., Boyd, P., Jordan, H., Stone, D., ...

Aims: To describe trends in total and live birth prevalence, regional differences in prevalence, and outcome of pregnancy of selected congenital anomalies. Methods: Population based registry study of...

Prevalence of congenital anomalies in five British regions, 1991-99. [In, Fetal and Neonatal Edition] (2005)

Rankin, J., Pattenden, S., Abramsky, L., Boyd, P., Jordan, H., Stone, D., ...

AIMS: To describe trends in total and live birth prevalence, regional differences in prevalence, and outcome of pregnancy of selected congenital anomalies. METHODS: Population based registry study of...

Congenital anomaly surveillance in England—ascertainment deficiencies in the national system (2005)

Boyd, P A, Armstrong, B, Dolk, H, Botting, B, Pattenden, S, Abramsky, L, ...

Objective Firstly, to assess the completeness of ascertainment in the National Congenital Anomaly System (NCAS), the basis for congenital anomaly surveillance in England and Wales, and its variation...

An aetiological classification of birth defects for epidemiological research (2005)

Wellesley, D., Boyd, P., Dolk, H., Pattenden, S.

Background: Congenital anomaly registers collect data on antenatally and postnatally detected anomalies for surveillance, research, and public health purposes. Each anomaly is coded using the...

Congenital anomaly surveillance in England-ascertainment deficiencies in the national system (2005)

Boyd, P.A., Armstrong, B., Dolk, H., Botting, B., Pattenden, S., Abramsky, L., ...

Objective Firstly, to assess the completeness of ascertainment in the National Congenital Anomaly System (NCAS), the basis for congenital anomaly surveillance in England and Wales, and its variation...

An aetiological classification of birth defects for epidemiological research (2005)

Wellesley, D., Boyd, P., Dolk, H., Pattenden, S.

BACKGROUND: Congenital anomaly registers collect data on antenatally and postnatally detected anomalies for surveillance, research, and public health purposes. Each anomaly is coded using the...

SHOX mutations in a family and a fetus with Langer mesomelic dwarfism (2004)

Thomas, N. S., Maloney, V., Bass, P., Mulik, V., Wellesley, D., Castle, B.

Léri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD) are caused by mutations in the SHOX gene. LWD results from haploinsufficiency and is dominantly inherited, while the more...

Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registers (2004)

Wellesley, D., De Vigan, C., Baena, N., Cariati, E., Stoll, C., Boyd, P.A., ...

The objective of this study was to evaluate the contribution of ultrasound scanning to the prenatal detection of trisomy 21 in a large unselected European population. Data from 19 congenital...

Unusual prenatal presentation of Beckwith-Wiedemann syndrome (2004)

Mulik, V., Wellesley, D., Sawdy, R., Howe, D.T.

When Beckwith-Wiedemann syndrome (BWS) is detected prenatally, it is usually on the basis of macroglossia, exomphalos or enlarged kidneys. We describe a case that presented as gross hepatomegaly and...

SHOX mutations in a family and a fetus with Langer mesomelic dwarfism (2004)

Thomas, N.S., Maloney, V., Bass, P., Mulik, V., Wellesley, D., Castle, B.

Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD) are caused by mutations in the SHOX gene. LWD results from haploinsufficiency and is dominantly inherited, while the more...

Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registers (2004)

Wellesley, D., De Vigan, C., Baena, N., Cariati, E., Stoll, C., Boyd, P.A., ...

The objective of this study was to evaluate the contribution of ultrasound scanning to the prenatal detection of trisomy 21 in a large unselected European population. Data from 19 congenital...

Congenital anomaly surveillance in England—ascertainment deficiencies in the national system

Boyd, P A, Armstrong, B, Dolk, H, Botting, B, Pattenden, S, Abramsky, L, ...

Objective Firstly, to assess the completeness of ascertainment in the National Congenital Anomaly System (NCAS), the basis for congenital anomaly surveillance in England and Wales, and its variation...

Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Foy, C, Newton, V, Wellesley, D, Harris, R, Read, A P

We have demonstrated close linkage between the locus for the autosomal dominant Waardenburg syndrome type I and the placental alkaline phosphatase locus on chromosome 2q37. In five families the peak...

Congenital anomaly surveillance in England—ascertainment deficiencies in the national system

Boyd, P A, Armstrong, B, Dolk, H, Botting, B, Pattenden, S, Abramsky, L, ...

Objective Firstly, to assess the completeness of ascertainment in the National Congenital Anomaly System (NCAS), the basis for congenital anomaly surveillance in England and Wales, and its variation...

Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Foy, C, Newton, V, Wellesley, D, Harris, R, Read, A P

We have demonstrated close linkage between the locus for the autosomal dominant Waardenburg syndrome type I and the placental alkaline phosphatase locus on chromosome 2q37. In five families the peak...

Asymmetry and skin pigmentary anomalies in chromosome mosaicism.

Woods, C G, Bankier, A, Curry, J, Sheffield, L J, Slaney, S F, Smith, K, ...

We report six persons mosaic for a chromosome anomaly. All were mentally retarded and dysmorphic. Unilateral or asymmetrical features were found in all cases, in one an unusual transverse terminal...

Simultaneous trisomy 9q3 and monosomy 5p in two children with der(5),t(5;9)(p15.1;q34.13): report of an extended family.

Wellesley, D, Young, I D, Cooke, P, Callen, D F, Hockey, A

We present a family segregating for t(5;9)(p15.1;q34.13). Two cases with der(5),t(5;9), resulting in a partial duplication 9q34.13----qter and partial deletion of 5p15.12----pter, were ascertained....

An aetiological classification of birth defects for epidemiological research

Wellesley, D, Boyd, P, Dolk, H, Pattenden, S

Background: Congenital anomaly registers collect data on antenatally and postnatally detected anomalies for surveillance, research, and public health purposes. Each anomaly is coded using the...

Prevalence of congenital anomalies in five British regions, 1991–99

Rankin, J, Pattenden, S, Abramsky, L, Boyd, P, Jordan, H, Stone, D, ...

Aims: To describe trends in total and live birth prevalence, regional differences in prevalence, and outcome of pregnancy of selected congenital anomalies.